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Abstract

Human papillomavirus (HPV) remains a major public health concern because infection with high-risk HPV types can lead to several cancers, including cervical cancer and cancers of the anal, penile, vulvar, vaginal, and oropharyngeal regions. HPV vaccines offer a preventive approach by training the immune system to recognize and block infection by HPV types most strongly linked to these diseases. In this study/review, we summarize how available HPV vaccines generate strong immune responses and how vaccination programs—especially when given before sexual exposure—can substantially lower rates of vaccine-type HPV infection and related precancerous changes. We also discuss real-world implementation factors such as age at vaccination, coverage levels, and catch-up strategies, since these determine how much benefit a community can achieve. Finally, the long-term success of HPV vaccination depends on ongoing surveillance of vaccine effectiveness and duration of protection, along with continued efforts to reduce barriers to access and improve public confidence. Overall, HPV vaccination is an evidence-based, cost-effective intervention that can prevent disease across the life course when delivered with high uptake.

Keywords

Human Papillomavirus (HPV), HPV Vaccination, Cervical Cancer Prevention, Vaccine Effectiveness, Immunization Programs

Introduction

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Human papillomavirus (HPV) is one of the most common sexually transmitted infections worldwide. It mainly affects the skin and mucous membranes of the genital area, mouth, and throat. In many cases, HPV infection does not cause any noticeable symptoms, although some types can lead to the development of warts.

Most HPV infections clear up naturally as the body’s immune system fights the virus, without the need for medical treatment. However, some high-risk types of HPV can persist in the body and, over time, may cause serious health problems. Persistent infection with these high-risk types has been linked to several cancers, including cervical cancer and cancers of the oropharynx (such as the tonsils and base of the tongue), anus, and penis.

HPV usually infects the basal cells, which are located in the deeper layers of the skin and mucous membranes. The virus can enter the body through very small cuts, scratches, or breaks in the skin. Once it enters these cells, HPV begins to multiply as the infected cells grow, mature, and gradually move toward the surface.

With certain high-risk types of HPV, particularly HPV 16 and 18, the virus can interfere with the normal functioning of the infected cells. In some cases, the viral DNA can become incorporated into the DNA of the host cell. This can cause the infected cells to produce viral proteins continuously, which interfere with the mechanisms that normally keep cell growth under control. Over time, these changes can cause abnormal cell growth and may increase the risk of cancer.

If the infection persists, the continued and uncontrolled growth of abnormal cells can eventually contribute to the development of cancer, including cervical cancer. In contrast, low-risk HPV types, such as HPV 6 and 11, are generally not associated with cancer. However, they can still cause health problems, most commonly genital warts.

History and Discovery of Human Papillomavirus

Human papillomaviruses (HPVs) are a large group of small, host-specific viruses that can infect a wide range of animal species, including humans. In humans, more than 200 types of HPV have been identified, with around 85 genotypes having been well characterized.

The connection between HPV and cervical cancer was established in the 1980s through the work of Harald zur Hausen. His research played a major role in demonstrating that certain HPV types are responsible for cervical cancer and ultimately earned him the 2008 Nobel Prize in Physiology or Medicine.

Most HPV infections are naturally cleared by the body’s immune system and do not cause serious health problems. However, when infection with high-risk HPV types, particularly HPV 16 and 18, persists, it can cause abnormal changes in cervical cells. Over time, these changes may progress to cervical cancer.

Several factors can increase the likelihood of persistent HPV infection and disease progression. These include smoking, long-term use of oral contraceptives, other sexually transmitted infections, the individual’s immune response, and characteristics of the virus itself. Recognizing HPV as the main cause of cervical cancer has led to significant advances in prevention, particularly through HPV vaccination and regular cervical cancer screening.

Classification and Types of Human Papillomavirus

1. Clinical Classification

High-Risk HPV (Oncogenic Types)

High-risk HPV types are those that have the potential to cause cancer, particularly when the infection persists for a long period. There are approximately 12–14 high-risk HPV types, including HPV 16, 18, 31, 33, 35, 45, 51, 52, 56, 58, 59, 66, and 68. Among these, HPV 16 and 18 are the most significant because they are responsible for approximately 70% of cervical cancer cases worldwide. Persistent infection with high-risk HPV types is also associated with cancers of the anus, penis, vulva, vagina, and oropharynx (throat).

Low-Risk HPV (Non-Oncogenic Types)

Low-risk HPV types are generally not associated with cancer. Instead, they commonly cause benign conditions such as genital warts and other minor cellular changes. HPV 6 and 11 are the most common low-risk types and are responsible for more than 90% of anogenital warts. These types can also cause recurrent respiratory papillomatosis, a condition in which benign growths develop in the respiratory tract.

2. Tissue Tropism

Mucosal/Anogenital Epithelium

Some HPV types have a preference for infecting the moist mucosal surfaces of the body. These include the vagina, cervix, vulva, penis, anus, mouth, and throat. HPV types that infect these areas are commonly referred to as mucosal or anogenital types.

Cutaneous Epithelium

Other HPV types primarily infect the outer layers of the skin rather than mucosal surfaces. These cutaneous HPV types are commonly associated with skin warts, including plantar warts and flat warts, which may occur on the hands, knees, and feet. Common cutaneous HPV types include HPV 1, 2, 3, 4, 27, and 57.

Figure 1:Types of warts

Structure and Genome of Human Papillomavirus

HPV is a small, non enveloped virus with a icosahedral capsid composed of L1 and L2 proteins, enclosing a circular double stranded DNA genome of about 8,000 basepairs as mentioned in fig.2

Figure 2: Structure of HPV

Capsid structure:

Human papillomavirus (HPV) is a small, non-enveloped virus with a diameter of approximately 50–60 nanometers (nm). It has an icosahedral structure, meaning that its protein shell, or capsid, has a highly organized geometric shape. The capsid consists of 72 pentameric capsomers, with each capsomer being formed by five molecules of the major capsid protein L1.

L1 is the most abundant viral structural protein and accounts for approximately 80% of the proteins in the viral capsid. It plays an important role in maintaining the characteristic icosahedral shape of the virus and is also involved in the initial attachment of HPV to host cells.

The minor capsid protein, L2, is present in much smaller amounts and has a molecular weight of approximately 70 kDa. Unlike L1, much of L2 is located within or beneath the capsid structure. L2 contributes to the stability and organization of the viral capsid and also plays an important role during viral entry into host cells. The capsid is further stabilized by intra- and inter-pentameric disulfide bonds, which help maintain its structural integrity

Transmission of Human Papillomavirus

Sexual Activity:

Sexual contact is the most common way HPV is transmitted. The virus can spread through direct skin-to-skin contact with infected genital areas, as well as through oral or genital contact involving the mouth and throat.

Asymptomatic Transmission:

HPV can often be transmitted by individuals who have no visible signs or symptoms of infection. Because many people are unaware that they carry the virus, they may unknowingly pass it on to their sexual partners.

Mother-to-Child Transmission:

In rare cases, a pregnant person with a genital HPV infection may transmit the virus to their newborn during vaginal delivery. Although uncommon, this can occasionally result in HPV-related conditions in the infant.

Non-Sexual Contact:

HPV may also be transmitted through non-sexual skin-to-skin contact, although this is considered much less common. For example, contact between infected hands and the genital area may provide an opportunity for transmission. Indirect transmission through contaminated objects, such as towels, has also been suggested, but HPV does not generally remain viable for long periods outside the body.

Pathogensis of human papillomavirus

Entry of the virus through sexual/direct contact/microabrasions

Infection of basal epithelium cells

Viral DNA replication in nucleus

E6 and E7 protein production

E6-Inactivation of p53

E7-Inactivation of Rb protein

Uncontrolled cell proliferation

Persistent and progression of infection

Cervical intraepithelial neoplasia(CIN)

Cervical cancer (high-risk HPV types)

Figure 3 : Pathogensis of HPV

Epidemology of Human papillomavirus infection

  • Indian scenario

In India, HPV-related cancers continue to be an important public health concern. A National Cancer Registry Programme study projected that around 121,302 HPV-related cancer cases could occur in India in 2025, accounting for approximately 7.7% of all cancer cases. The projected burden was higher among females (12.0%) than males (3.3%). Cervical cancer represents a major proportion of HPV-related cancers among women in the country.

Cervical cancer remains a major health concern for women in India and continues to contribute substantially to the global burden of the disease. The high number of cases highlights the importance of improving awareness about HPV, encouraging regular cervical cancer screening, and increasing access to HPV vaccination. Early detection and timely treatment can significantly improve outcomes and help reduce deaths associated with cervical cancer.

Recognizing the importance of prevention, the Government of India launched a nationwide HPV vaccination programme on 28 February 2026. Prime Minister Shri Narendra Modi launched the programme in Ajmer, Rajasthan, targeting approximately 1.15 crore girls aged 14 years across the country. The vaccine is being provided free of cost at government health facilities as part of the national effort to prevent cervical cancer.

The introduction of nationwide HPV vaccination, together with cervical cancer screening, early diagnosis, and appropriate treatment, represents an important step toward reducing the burden of HPV-related disease in India. These preventive measures can play a major role in protecting women’s health and moving the country closer to the goal of cervical cancer elimination.

  • Global scenario

Table 1: Global burden of HPV

Category

Information

Global HPV prevalence

11-12% of women without cervical abnormalities are infected with HPV.

Highest HPV prevalence by region

Sub-Saharan Africa:24%

Eastern Europe:21%

Latin America:16%

Most common HPV types

HPV 16:3.2%

HPV 18:1.4%

Association with cervical disease

HPV prevalence increases with the severity of cervical lesions. Approximately 90% of women with invasive cervical cancer are HPV-positive

HPV -associated cancers

Cervix, Penis, Vulva, Vagina, Anus, Oropharynx(base of the tongue and tonsils)

Global cancer burden (2008)

Total cancers:12.7 million

HPV-attributable cancers:610,000 (4.8%)

Cervical cancer: 530,000(86.9% of HPV-related cancers)

Others five HPV-related cancers:~80,000 cases

Regional variation in HPV-attributable cancers (Population Attributable Fraction, PAF)

India:15.5%

Sub-Saharan Africa:14.2%

Less developed regions:6.9%

More developed regions:2.1%

North America:1.6%

Australia/New Zealand:1.2%

Cervical cancer burden

Third most common cancer among women worldwide; accounts for 86.9% of all HPV related cancers.

Risk factors for HPV infection

Primary Risk factors

  • Number of sexual partners - having multiple partners.
  • Age - Occur most frequently in adolescents and young adults ,common skin warts primarily affect children.
  • Weakened immune system - Conditions like HIV/AIDS or taking immunosuppressive drugs impair body’s ability to naturally clear virus.
  • Damaged skin -Areas of the skin that are punctured, opened, injured are more prone to developing non-genital common warts.

Secondary Risk factors for Severe strains and complications

Certain behaviours and factors do not directly cause initial infection but are heavily linked to high-risk HPV persistence and progression to conditions like cervical cancer.

  • Smoking tobacco -impairs cervical immunity ,making it harder to clear high-risk strains.
  • Long-term oral contraceptive use -using birth control pills for 5 years or longer is statistically linked to a higher risk of cervical cancer in HPV-positive individuals.
  • Early sexual activity -Becoming sexually active at young age elevates lifetime exposure risks.

Figure 4 : Risk factors of HPV

Clinical manifestation of HPV infection

Table 2: Clinical manifestations of HPV

Clinical form

Common HPV Strains

Primary body sites

Visible Signs and Lesions

Clinical symptoms

Common warts

HPV-2, HPV-4

Hands, fingers, around nails

Rough, raised, skin-coloured bumps; tiny black dots.

Usually painless; cosmetic concern.

Plantar warts

HPV-1,HPV-2

Soles of the feet

Hard, thick, flattened growths that interrupt foot lines.

Sharp pain when walking or standing.

Flat warts

HPV-3, HPV-10

Face, arms, legs, back of hands.

Small(1-5mm), smooth, flat-topped, brownish bumps.

Often appear in large groups or lines.

Genital warts

HPV-6, HPV-11

Penis, vulva, scrotum, cervix, anus

Soft, flesh-colored, pink, or gray bumps; can look like tiny cauliflowers.

Itching, mild burning, discomfort, or bleeding.

Respiratory papillomas

HPV-6, HPV-11

Larynx, vocal cords, airway

Small, wart-like tumors inside respiratory tract.

Chronic cough, breathing trouble.

Cervical Dysplasia and cancer

HPV-16, HPV-18

Uterine cervix (transformation zone)

Early stages are invisible; advanced stages show cervical ulcers/masses.

Early: asymptomatic (detected via Pap/HPV test).Late: Abnormal bleeding, pelvic pain.

Other Mucosal cancers

HPV-16, HPV-18

Anus, vulva, vagina, penis

Non-healing ulcers, structural changes, or hard lumps on tissues.

Chronic itching, bleeding, pain, or visible growths.

Oropharyngeal cancer

HPV-16

Base of tongue, tonsils, throat

Tumors or tissue changes at the back of the mouth and throat.

Persistent sore throat, difficulty swallowing, neck lump.

Figure 5: Clinical manifestations of HP

HPV associated diseases

  • HPV-associated Cervical cancer

Cervical cancer is the fourth most common cancer among women worldwide and remains a major public health program , particularly in low-and middle-income countries.

Persistent infection with high-risk HPV is recognized as the necessary cause of nearly all cervical cancers, with HPV-16 and HPV-18 accounting for approximately 70% of cases.

  • HPV-associated Anal cancer

Anal cancer is relatively uncommon but has shown increasing incidence globally.

Approximately 85-95% of anal squamous cell carcinomas are attributable to persistent infection with high-risk  HPV, particularly HPV-16.

  • Other HPV-associated Malignancies

Persistent infection with high-risk HPV is also implicated in several other cancers, including:

  • Oropharyngeal cancer, particularly involving the tonsils and base of the tongue.
  • Vulvar cancer
  • Vaginal cancer
  • Penile cancer

HPV-16 is the predominant genotype responsible for most HPV-associated cancers outside the cervix.

Diagnosis and screening of HPV infection

Human Papillomavirus (HPV) screening and diagnostic primarily target the early detection of high-risk viral strains to prevent cervical cancer.

  1. Primary Screening Methods

Screening tests check for the presence of the virus or abnormal cell changes before symptoms develop.

  • Primary HPV Test: this molecular lab test directly looks for the DNA or RNA of high -risk HPV types (such as HPV 16 and 18) in cervical cells.
  • Pap Smear (cytology):Clinician collects cells from cervix to look for precancerous changes under a microscope. It identifies cellular damage caused by the virus rather than virus itself.
  • Co-Testing: This approach performs both primary HPV test and a Pap smear simultaneously using same collected sample.
  1. Standard Screening Guidelines

Major health organizations like the World Health Organization (WHO) and the American Cancer Society recommend the following timelines for average-risk individuals:

  • Under Age 21: Screening is not recommended.
  • Ages 21-29: A standalone Pap smear every 3 years is standard.
  • Ages 30-65: Primarily HPV testing or Co-testing every 5 years is highly preferred. Alternatively, a standalone Pap smear every 3 years is acceptable.
  • Over Age 65: Screening can stop if previous consecutive test results have been consistently negative.
  • Immunocompromised Individuals: Individuals living with HIV require more frequent intervals, starting at age 25 and repeating every 3 years.
  1. Diagnostic Procedures for Abnormal Results

If a screening test comes back abnormal or positive for a high-risk, secondary diagnostic steps confirm the severity of the infection:

  • Colposcopy: A specialized, lighted magnifying tool examines the cervix , vagina and vulva for abnormal tissue.
  • Biopsy: The clinician removes a small tissue sample during a colposcopy for pathological testing to check cervical interepithelial neoplasia(CIN).
  • Visual inspection with acetic acid (VIA):Used primarily in low-resource settings, a vinegar solution applied to cervix turns HPV-affected areas white for immediate visual tracking.
  • Clinical Visual Exam: Low-risk HPV strains cause external genital warts, which healthcare providers typically diagnose through a standard physical examination without molecular tests.

Figure 6: Screening and diagnosis of HPV

Human papilloma virus Vaccine

Figure 7: HPV Vaccine

  • The HPV vaccine is a key to addressing the disproportionate distribution of cervical cancer    with much to be gained from increasing vaccine coverage and uptake globally.
  • HPV vaccination provide safe, effective, and long lasting protection against HPV infection that most commonly causes cancer.
  • The Human papillomavirus vaccine was officially introduced as a free nationwide campaign in India on February 28, 2026 for approximately 1.2 crore eligible beneficiary girls aged 14 years by Prime Minister Narendra Modi.

Figure 8: HPV Vaccination Campaign in India

  • Countries like India, United States, United Kingdom, China have successfully introduced national HPV vaccination programmes are on course for cancer elimination in a few decades.
  • The countries that lack structured screening and HPV vaccination programmes, cervical cancer remains a major cause of morbidity and mortality.
  • One of the important medical cases, an African American woman died from cervical cancer seventy years ago, at the age of 32. HeLa cells, as they are commonly referred to, are the cells which were collected from her cervix in 1951 shortly before her death, these were the first established in vitro immortal cancer cell line and have formed the basis for multiple advances in medical research including the development of the Human Papillomavirus (HPV) vaccine.

Types of HPV vaccine

  1. Bivalent Vaccine (HPV2)
  • Brand Name:  Cervarix
  • Target Strains: Types 6, 11, 16, and 18 (Includes cancer-causing strains plus 6 and 11, which cause 90% of genital warts)
  • Composition per 0.5ml dose:
  • 20 μg of HPV 16 L1 protein and 20 μg of HPV 18 L1 protein.
  • Adjuvant: AS049 (composed of aluminium hydroxide and 3-deacylated monophosphoryl lipid A) to boost immune response.
  1. Quadrivalent Vaccine (HPV4)
  • Brand Name: Gardasil, Cervavac
  • Target Strains: Types 6, 11,16, and 18( includes cancer-causing strains plus 6 and 11, which cause 90% of genital warts)
  • Composition per 0.5ml dose(e.g., Gardasil):
  • 20 μg HPV 6, 40 μg HPV 11, 40 μg HPV 16, 20 μg HPV 18.
  • Adjuvant: Amorphous aluminium hydroxyphosphate sulphate.
  1. Nonavalent Vaccine (HPV9)
  • Brand Name: Gardasil 9
  • Target Strain: 6, 11, 16, 18, 31, 33, 45, 52, 58 (the broadest protection, covering cancer-causing strains that account 90% of cervical cancer).
  • Composition per 0.5ml dose:  
  • Contains L1VLPs for all 9 strains
  • Adjuvant: Amorphous aluminium hydroxyphosphate sulphate.

Mechanism of Action:

HPV vaccine is a immunisation that works by stimulating the body to produce antibodies.

It uses hollow Virus-like particle (VLPs) made of the virus’s major capsid protein (L1).

As these Virus-like particle lacks viral DNA, they are completely infectious.

The immune system recognises the VLPs as foreign, actively priming antigen-presenting cells to generate long lasting antibodies and immunological memory

Antibodies binds to the virus, preventing it from entering mucosal cells

Prevents HPV infection, Cervical cancer and other HPV-related disease

Dose Schedule:

  • HPV vaccine Schedule depends on the person age at the time of the first dose.

Number of Doses

Age

Duration

Two Dose

  • First Dose.
  • Second Dose.

9 to 14 years.

After completion of first dose. Second dose is taken after 6 to 12 months.

Three Dose

  • First dose.
  • Second dose.
  • Third dose.

15 and above age.

 

After completion of first dose. Second dose is taken after 2 months. Third dose is taken after 6 months.

  • The younger recipients need fewer doses due to their immune system mount a strong antibody response to each dose.
  • Two doses in a younger recipients produce antibody levels comparable to three doses in above 20 years recipient.
  • Whereas the people above 25 years follows the three-dose schedule due to weaker immunity.
  • Pregnant women, people with moderate or severe illness, and people with allergic conditions are restricted to receive HPV vaccination.

Prevention of HPV

  • Prevents cervical cancer:  HPV Is responsible for nearly all cases of cervical cancer
  • Reduce other HPV-related cancers: It also helps to prevent cancers of the anus, vulva, vagina, penis, and the throat (oropharynx).
  • Prevents genital warts: The vaccine protects against HPV types that cause most genital warts.
  • Most effective before sexual activity begins: Vaccination before HPV exposure provides the strongest protection.
  • Long-lasting protection: Studies have shown durable immunity for many years after vaccination.
  • Reduces disease burden: Widespread vaccination lowers HPV transmission and decreases the incidence of HPV-related disease in the population.
  • Safe and effective: Extensive research and ongoing monitoring have demonstrated that HPV vaccines have a strong safety profile and are highly effective at preventing infections with the targeted HPV types.
  • Reduces transmission: Vaccinating both girls and boys decreases HPV circulation in the community, providing herd protection and reducing overall disease burden.
  • Cost-effective prevention: Vaccination is far less expensive and less invasive than treating HPV-related cancers screening and precancerous lesion.
  • Complements cervical cancer screening: Although vaccinated women should still undergo routine cervical screening, vaccination greatly reduces the likelihood of developing high-grade cervical lesions and cervical cancer.
  • Excellent safety profile: HPV vaccines have been extensively studied and are considered safe, with most adverse effects being mild and temporary, such as pain at the injection site or low-grade fever

WHO Recommendations:

  • Primary target group: Girls aged 9-14 years, preferably before sexual debut.
  • Boys: Vaccination is also recommended in many countries to prevent HPV-related disease and reduces transmission.
  • Catch-up vaccination: Recommendation up to 26 years for individual who were not vaccinated earlier. Adults aged 27-45 years may benefit based on individual risk after discussion with a healthcare provider.
  • Avoids HPV Transmission: Helps in reducing the spread of HPV through sexual contact. However, it does not completely block transmission. Therefore, precaution is necessary.
  • Protects Against Genital Warts: The Quadrivalent and nine-valent types provides protection against HPV types responsible for approximately 90% of genital warts.
  • Protects Against Cervical Cancer: The HPV vaccine for women protects against HPV types that causes about 70% of cervical cancer cases.
  • Reduces Risk of Other Cancer: Lowers the chance of developing anal, vulvar, vaginal, penile, and oropharyngeal cancers.
  • Provides Long-Lasting Protection: Offers strong immunity that can last more than a decade with no need for booster doses.
  • Boosts Herd Immunity: Widespread vaccination helps to protect people who are unvaccinated or have weaker immune system.

Side Effects of HPV Vaccine

HPV vaccine side effects are generally mild and temporary which involves

  • Swelling and redness
  • Pain at the site of injection
  • Tiredness
  • Nausea
  • Mild fever
  • Muscle pain.

AIM:

To evaluate the importance, safety, efficacy, and public health impact of the Human Papillomavirus (HPV) vaccine in preventing HPV-related infections and cancers, while promoting awareness about its role in disease prevention.

Objectives:

  1. To understand the Human Papillomavirus (HPV), its types, modes of transmission, and associated diseases.
  2. To study the mechanism of action of the HPV vaccine and how it provides immunity against HPV infection.
  3. To evaluate the effectiveness of the HPV vaccine in preventing cervical cancer and other HPV-related cancers and diseases.
  4. To assess the safety profile of the HPV vaccine, including common adverse events and rare adverse reactions through pharmacovigilance data.
  5. To examine the recommended vaccination schedule, target population, and current immunization guidelines.
  6. To analyze the role of the HPV vaccine in reducing the global burden of cervical cancer and improving public health.
  7. To identify barriers to HPV vaccination, such as lack of awareness, vaccine hesitancy, and accessibility, and suggest strategies to improve vaccine uptake.
  8. To emphasize the importance of pharmacovigilance in monitoring the long-term safety and effectiveness of HPV vaccines after their introduction into immunization programs.

REVIEW OF  LITERATURE

Saeeda Wasim et al., (2026) published on HPV Vaccination: Broader Implementation and Development of Next-Generation Vaccines Reduce the Incidence of Cervical Cancer

The protective effectiveness of prophylactic HPV vaccination has been firmly established through rigorous randomized controlled trials, as well as extensive long term observational studies conducted alongside national immunization programs. Together, these studies provide strong and reliable evidence demonstrating the vaccines significant benefits for public health. The scientific evidence is comprehensive and widely accepted, highlighting the important role of HPV vaccination in preventing HPV-related diseases and improving population health.

Cervical cancer continues to be significant global health challenge, with persistent infection by high risk Human Papillomavirus (HPV) identified as the primary etiological factor. Prophylactic HPV vaccination represents the most effective strategy for the primary prevention of cervical cancer. Extensive real-world evidence from national immunization programs implemented across multiple countries has consistently demonstrated the effectiveness of HPV vaccination. These programs have shown a marked reduction in the incidence of high grade cervical intraepithelial neoplasia (CIN2+ and CIN3+) and more importantly, a significant decrease in the risk of invasive cervical cancer among individuals vaccinated during early adolescence. The greatest protective benefit has been observed in cohorts immunized before exposure to HPV, understanding the importance of early vaccination. Collectively, these findings provide compelling evidence supporting the widespread implementation of HPV vaccination programs as a cornerstone of global cervical cancer prevention strategies.

Anna Beltrame et al., (2026) published on Impact of Male Human Papillomavirus (HPV) Vaccination on HPV Infection and HPV-related Diseases

Human papillomavirus (HPV) is the most prevalent sexually transmitted infection worldwide and is major cause of anogenital warts and several HPV-related cancers. Although the effectiveness of HPV vaccination in females has been extensively documented since its introduction in 2006, evidence regarding the impact of male vaccination programs has emerged more recently. Studies conducted in high-income countries examined the effects of gender-neutral vaccination(GNV) by comparing outcomes before and after implementation of male vaccination programs. The review found consistent evidence that GNV has contributed to improved  health outcomes among males. Reductions were observed in vaccine-targeted HPV infections and in the incidence of anogenital warts, particularly among adolescents and young adults. However, the authors noted that some of these benefits may also be influenced by herd immunity resulting from earlier female-only vaccination programs. Although the overall incidence of HPV-related cancers remained high, likely due to the long latency period between HPV infection and cancer development, encouraging declines were reported among younger male populations. These included reductions in oropharyngeal, penile, and anal cancers in countries such as the United States, Australia, and specific regions of Texas. The review concluded that, because male HPV vaccination programs have been implemented relatively recently, continued long-term surveillance is essential to accurately determine their full impact on reducing HPV-related cancers.

Uma Vasudevan et al., (2026) published on marginalized voices on HPV vaccination in India

A recent study explored the knowledge, attributes, and acceptability of Human Papillomavirus (HPV) vaccination among marginalized communities in India, where cervical cancer continues to be significant cause of illness and death among women. Conducted across three diverse settings, the study was undertaken in preparation for the national rollout of HPV vaccination for girls ages 9-14 years. The findings emphasized that marginalized populations often have limited awareness of HPV, cervical cancer, and the benefits of vaccination, which may hinder vaccine uptake. The study highlighted the importance of understanding community perceptions, cultural beliefs, and potential barriers to vaccination in order to ensure equitable access and acceptance. The authors concluded that community-based education, culturally appropriate awareness campaigns, and strategies that address the specific needs of underserved populations are essential for the successful implementation of India’s national HPV vaccination program and for reducing disparities in cervical cancer prevention.

Agapiti H. Chuwa (2026) published on Innovations in HPV vaccination and their global cervical cancer control

Cervical cancer remains a major global health concern, particularly in sub-Saharan Africa, where persistent infection with high-risk HPV types, especially HPV-16 and HPV-18, contributes significantly to disease burden. A review of HPV vaccine development highlighted the effectiveness of bivalent, quadrivalent, and nonvalent vaccines in preventing HPV infections and cervical lesions through strong immune responses. The introduction of affordable vaccines such as cecolin and cervavac, along with the WHO-recommended single-dose schedule, has improved opportunities for expanding vaccination coverage in low-and middle-income countries. However, challenges such as limited healthcare access, vaccine hesitancy, and lack of awareness continue to affect global vaccine uptake. The review emphasized that combining advances in vaccine technology with effective public health strategies is essential for achieving cervical cancer elimination goals.

Mengdi Ji et al., (2025) published on HPV vaccination coverage, hesitancy and barriers

Cervical cancer remains one of the leading causes of cancer related-morbidity and mortality among women worldwide, with China contributing nearly one-fifth of the global disease burden. Recognizing the effectiveness of the Human papillomavirus (HPV) vaccine in preventing high-risk HPV infections and cervical cancer, researchers conducted a serial cross-sectional study in Shanghai to examine to changes in HPV vaccination uptake and vaccine hesitancy between 2019 and 2024. The findings demonstrated a substantial increase in HPV vaccination coverage, rising from 6% to 30% over the five-year period. However, vaccination rates among girls aged 9-14 years, the primary target group recommended by the World Health Organization (WHO), remained low at only 8%. The study further identified HPV-specific vaccine hesitancy as a major barrier to vaccine uptake, with hesitant parents being significantly less likely to vaccinate their daughters. General vaccine hesitancy also negatively influenced vaccination, although its contribution to non-vaccination was smaller than that of HPV-specific concerns. Population Attributable Fraction analysis showed that HPV-specific hesitancy accounted for a considerable proportion of missed vaccinations, emphasizing the need for interventions that directly address misconceptions and concerns related to the HPV vaccine. Concluded that improving public awareness, promoting timely vaccination among the recommended age group, and addressing practical barriers to vaccine access are essential strategies for increasing vaccine coverage and supporting global efforts toward the elimination of cervical cancer.

Wojciech Miazga et al., (2025) published on Global Guidelines and Trends in HPV Vaccination for Cervical Cancer Prevention

Cervical cancer remains a major global health challenge, with persistent high-risk HPV infection as its primary cause. HPV vaccination is the most effective strategy for preventing HPV infection and reducing cervical cancer incidence. This review analyzed 16 clinical guidelines published between 2019 and 2024 and found strong international consensus on routine HPV vaccination before 15 years of age, preferably before sexual debut. Most guidelines recommend gender-neutral vaccination, with the 9-valent Gardasil 9 vaccine as the preferred option. The Who’s 2022 recommendation of a single-dose schedule is expected to improve vaccine access, reduce costs, and increase coverage, particularly in low-and middle-income countries. Expanding early, gender-neutral vaccination and simplified schedules will support the global goal of eliminating cervical cancer as a public health problem.

Anuradha Nadda et al., (2024) published on IAPSM’s Position paper on the Human papillomavirus (HPV) Vaccine for Adult Immunization in India

Cervical cancer remains one of the leading causes of cancer-related morbidity and mortality among women in India, ranking as the second most common cancer affecting women. Persistent infection with the Human papillomavirus (HPV), particularly high-risk HPV types, has been identified as the primary cause of cervical cancer. Because the disease develops over a prolonged latent period, secondary prevention through regular screening and early detection plays a crucial role in reducing its incidence and mortality. However, the uptake of screening services in India continues to be limited due to factors such as fear of a cancer diagnosis, social stigma, lack of awareness, and the financial burden associated with treatment.

Recent literature highlights HPV vaccination a the most effectiveness strategy for the primary prevention of cervical cancer. India currently has four prophylactic HPV vaccines available for use. These vaccines are non-infectious, highly immunogenic safe, and demonstrate high efficacy when administered before exposure to HPV. National and international guidelines recommend vaccination primarily for girls aged 9-14 years, as immunization before the onset of sexual activity provides maximum protection against HPV infection.

Evidence from recent studies further indicates that both single-dose and two-dose HPV vaccination schedules provide comparable protection and effectiveness against HPV infection, making vaccination programs more feasible and cost-effective, particularly in resource-limited settings. The vaccines are administered intramuscularly in the deltoid region at a standard dose of 0.5mL. Although mild adverse effects such as pain at the injection site, headache, and myalgia have been reported, these reactions are generally transient and resolve without serious complications.

Several studies also emphasize the importance of implementing catch-up vaccination programs for girls aged 9-14 years during the introduction of HPV vaccination initiatives. Such an approach has been shown to be both cost-effective and sustainable, increasing vaccine coverage and accelerating the reduction of HPV-related disease burden. Overall, the literature supports HPV vaccination as a key public health intervention that, when combined with effective screening programs, has the potential to significantly reduce HPV infections and contribute to the long-term elimination of cervical cancer in India.

Pei-Jen Lou et al., (2024) published on Systematic literature review on the clinical and economic burden of human papillomavirus-related diseases in select areas in the Asia-Pacific region

A systematic literature review examined the burden of human papillomavirus (HPV) and HPV-related diseases across selected Asia-Pacific (AP) countries, where the implementation of national HPV vaccination programs has lagged behind that of Europe and North America. The review included 254 observational studies published between 2000 and 2022, assessing the incidence, prevalence, healthcare resource utilization, and economic burden of HPV-related diseases among adults. The findings revealed a substantial burden of HPV-associated cancers, including cervical, head and neck, anal, penile, and vaginal or vulvar cancers, with considerable variation in reported incidence and prevalence across countries. Although relatively few studies evaluated healthcare costs and resource utilization, the available evidence suggested that HPV-related diseases impose a significant clinical and economic burden on healthcare systems in the region. The authors attributed the observed variability to differences in study design, surveillance systems, and data availability across countries. Despite these limitations, the review emphasized the urgent need to strengthen HPV prevention strategies through expanded vaccination programs, effective screening initiatives, public education to reduce vaccine hesitancy , and improved disease surveillance. The authors further highlighted the importance of generating high-quality epidemiological data, particularly in low-and middle-income settings within the Asia-Pacific region, to support evidence-based policy decisions and to monitor the long-term impact of HPV vaccination programs.

Elizabeth Goodman et al., (2022) published on Human Papillomavirus Vaccine Impact and Effectiveness

Specific adult populations known to be at high risk for human papillomavirus (HPV) related disease, such as men who have sex, are inconsistently included in national immunization programs. No complications of the evidence on the real-world impact and effectiveness of HPV vaccines in high-risk populations exists. This review identifies and synthesizes the evidence of the real-world impact and effectiveness of the quadrivalent and nonavalent HPV vaccines in high-risk populations: women with prior/current HPV-related anogenital disease, men who have sex with men, immunocompromised/immunosuppressed individuals, female sex workers, transgender and non-binary individuals, and patients with recurrent respiratory papillomatosis (RRP). The outcomes included anogenital precancers/cancers, head and neck cancers, genital warts, and RRP recurrence. The results, quantity, quality of these studies were highly variable. The evidence for effectiveness was of high quality only in women with prior/current cervical disease and in individuals with RRP, the most frequently studied populations. No studies of transgender/non-binary individuals or female sex workers were identified. The real-world evidence supports HPV vaccination among women with prior cervical disease and individuals with RRP. Significant real-world data gaps remain in these high-risk populations.

Mallory K. Ellingson et al., (2022) published on Human Papillomavirus vaccine effectiveness by age at vaccination

The effectiveness of Human Papillomavirus (HPV) vaccination according to the age at which the vaccine was initiated or completed. The review analyzed studies published between 2007 and 2022 that evaluated vaccine effectiveness against vaccine-type HPV infections, anogenital warts, cervical abnormalities, and cervical cancer. The findings consistently demonstrated that HPV vaccination is most effective when administered before exposure to the virus, particularly during early adolescence. Vaccine effectiveness among individuals among individuals vaccinated between the ages of 9 and 14 years ranged from approximately 74% to 93%, whereas effectiveness among those vaccinated between 15 and 18 years showed greater variability, ranging from 12% to 90%. These results indicate that earlier vaccination provides stronger protection against HPV-related diseases, supporting current recommendations for routine vaccination before the onset of sexual activity. The authors concluded that timely HPV vaccination during early adolescence is essential for maximizing vaccine effectiveness and reducing the long-term burden of HPV-associated diseases.

Sean A. Hebert et al., (2018) published on Acceptance of HPV Vaccination in Kidney Transplant Recipients

A survey-based study investigated the factors contributing to the low uptake of the Human Papillomavirus (HPV) vaccine among kidney transplant recipients, a population at increased risk of HPV-related malignancies because of long-term immunosuppression. The study found that only 32% of eligible transplant recipients had initiated or complete the HPV vaccination series at the time of the survey, despite the protective benefits of the nonavalent HPV vaccine (Gardasil 9). The most significant barrier to vaccine initiation was the lack of a strong recommendation from healthcare providers. Following the survey, participants received brief educational information about the risks of HPV infection and benefits of vaccination, resulting in a notable increase in vaccine initiation, from 32% to 62%. These findings highlight the critical role of physician recommendation and patient education in improving HPV vaccine uptake among high-risk populations. The authors concluded that integrating routine vaccine counselling into post- transplant care could substantially increase vaccination rates and reduce the future burden of HPV-related cancers in kidney transplant recipients.

METHODOLOGY -

STUDY DESIGN-

Cross sectional, Prospective, Retrospective, Questionnaire based descriptive study.

DATA SOURCE-

  1. Primary source-Literatures published during 2018-2026 that provided relevant data were added.
  2. Secondary source-Literatures, articles and other reliable sources published from 2018-2026 were studied.
  3. Data collected from OP departments of the hospitals mentioned below:
  • Spandana health clinic.
  • Vediika child care.
  • Sunray hospital.

INCLUSION CRITERIA

  • Relevant literatures and published articles published during 2018-2026 were included to support study.
  • Participants who have provided the required information and shared relevant medical data for the study.

EXCLUSION CRITERIA

  • Literatures and articles that did not support the study were excluded.
  • Participants who have not provided information or shared relevant medical data for the study.
  • Chronic ill patients.

STUDY PROCESS

  • It was collected from relevant literatures as mentioned in the inclusion criteria to obtain the information and support the study.
  • It was obtained from relevant literatures, including published research articles, journals, and other reliable sources, to provide information and support the study.
  • Hospital data-Data were collected directly from the hospitals with consent from the patients for the study purpose.
  • Questionnaire administration-A structured Google Forms questionnaire was distributed to collect the required study information.
  • Data analysis-The collected data were complied, verified, and analysed using appropriate statistical methods.

DATA COLLECTION :

PATIENT DETAILS :

Sr. No

Name

Age/ gender

Dose

Suggestion

Brand

01

Karparaksha

24/Female

0,2

Self

Gardasil 9

02

Lakshanasri

10/Female

0,2

Self

Gardasil 9

03

Anitha Princy

30/Female

(0,2)

Self

Cervavac

04

Megha

27/female

(0,2)

Self

Cervavac

05

Deepanjali

16/Female

(0,2)

Self

Cervavac

06

Thaniksha

14/Female

(0,6)

Self

Cervavac

07

Akshana

10/Female

(0,6)

Self

Cervavac

08

Yazhini

10/Female

(0,6)

Self

Cervavac

09

Smitha

22/Female

(0,2)

Self

Cervavac

10

Kurparaksha

24/Female

(0,2)

Self

Gardasil 9

VEDIIKAA CHILD CARE

Dr. Loganayaki Vediikaa Renukanth,

MBBS., MD., DNB.,

Reg No. 83406

Cell: 7708515557

Sr. No

Name

Age/ gender

Dose

Suggestion

Brand

1

Kavinya

10 / Female

(0, 2)

Self

Gardasil 9

2

Aaradhya

14/ Female

(0, 2)

Self

Gardasil 9

3

Revathi

12/ Female

(0,2)

Self

Gardasil 9

4

Tamilselvi

15/ Female

(0,2)

Self

Gardasil 9

5

Bavya

16/ Female

(0,6)

Self

Gardasil 9

6

Deepasri

11/ Female

(0,2)

Self

Gardasil 9

7

Jeevitha

14/ Female

(0,6)

Self

Gardasil 9

8

Krishika

16/ Female

(0,2)

Self

Gardasil 9

9

Meena

13/ Female

(0,6)

Self

Gardasil 9

10

Sobiya

22/ Female

(0,2)

Self

Cervavac

11

Santha

27/ Female

(0,2)

Self

Cervavac

12

Roshini

16/ Female

(0, 2)

Doctor suggested

Cervavac

13

Vishnupriya

12/ Female

(0, 2)

Self

Cervavac

14

Hemalatha

14/ Female

(0,6)

Self

Cervavac

15

Ashwini

16/ Female

(0, 2)

Self

Cervavac

Sunray Hospital

Lightens your path

No.926/927/928, M S Complex, Near Chandapura Circle, Next to Karur Vysya Bank, Chandapura, Anekal Taluk, Bengaluru-560081

Web : www.sunrayhospitalbangalore.com

Contact : 8150024454 / 8150044020

Email : care.sunrayhospital@gmail.com

PATIENT DETAILS:

Sr. No

Name

Age/ gender

Date

Dose

Suggestion

Brand

1

Druthi

25/Female

24/03/2026

25/05/2026

1,2

Doctor

Gardasil 4

2

Pooja

27/Female

27/03/2026

1

Self

Gardasil 9

3

Revathi

36/Female

20/04/2026

28/05/2026

1,2

Doctor

Gardasil 9

4

Priyanka

32/Female

29/04/2026

1

Doctor

Gardasil 9

5

Lavanya

30/Female

14/05/2026

25/06/2026

1,2

Doctor

Gardasil 9

6

Divya. G

27/Female

15/05/2026

1

Doctor

Gardasil 9

7

Pavana S N Gowda

11/Female

18/05/2026

1

Doctor

Gardasil 4

8

Saraswathi

32/Female

05/07/2026

1

Self

Gardasil 9

9

Kalavathy

41/Female

17/06/2026

08/07/2026

1,2

Doctor

Gardasil 9

10

Pushpavathi

41/Female

06/06/2026

13/07/2026

1,2

Doctor

Gardasil 4

11

Adharsh

27/Male

16/06/2026

1

Doctor

Gardasil 9

12

Trupthi

16/Female

24/06/2026

1

Doctor

Gardasil 9

13

Moksha

35/Female

08/07/026

1

Doctor

Gardasil 4

Figure 9: Gardasil Vaccines

Repor

1. To understand the Human Papillomavirus (HPV), its types, modes of transmission, and associated diseases.

  

 

HPV types:

Low-Risk Types: Strains like HPV 6 and 11 cause benign lesions and genital warts.

High-Risk Types: Strains like HPV 16,18,31, and 45 cause precancerous lesions.

Uncontrolled high-risk infections can integrate into cells and cause cancer.

Mode of Transmission:

Sexual Activity is most common frequent method of transmission.

Asymptomatic Spread Transmitted by individuals with no visible signs

Mother to Baby Happens if the mother has an active gential infection.

Non-Sexual Contact Infrequent route of transmission

Associated Diseases:

Cancer: Cervical, oropharyngeal(throat), anal, penile, vaginal, and vulvar cancers.

Non-Cancer: Genital warts and recurrent respiratory papillomatosis(benign airway tumors).

2. To study the mechanism of action of the HPV vaccine and how it provides immunity against HPV infection.

HPV vaccine protects the body by creating antibodies that block the virus from entering cells. HPV vaccine prevents infection by introducing harmless virus-like particles into the muscle, which are quickly detected by immune cells. This detection activates B cells to produce high levels of specific, neutralizing antibodies. If the body encounters the actual HPV virus later, these antibodies immediately bind to it and block its entry into host cells, establishing long-term immunity.

3. To evaluate the effectiveness of the HPV vaccine in preventing cervical cancer and other HPV-related cancers and diseases.

The HPV vaccinee introduces harmless, non-infectious virus-like particles into the body to trigger a protective immune response. Upon injection, the body creates targeted antibodies against specific viral strains covered vaccine. If the individual is exposed to the live virus later, these circulating antibodies bind to it immediately. This action blocks the virus from entering and infecting healthy epithelial cells. By preventing a persistent infection, the vaccine stops the development of abnormal cellular mutations. Consequently, this process prevents long-term HPV-related cancers and genital warts.

4. To assess the safety profile of the HPV vaccine, including common adverse events and rare adverse reactions through pharmacovigilance data.

 
  • HPV vaccines are generally safe and well tolerated.
  • Common adverse events include pain, redness, swelling, headache, fatigue, fever, and nausea, which are usually mild and temporary.
  • Rare reactions such as severe allergy nd fainting are monitored closely.
  • Pharmacovigilance continuously collects and evaluates safety data to ensure the vaccine remains safe and its benefits outweigh the risks.

5. To examine the recommended vaccination schedule, target population, and current immunization guidelines

HPV VACCINATION RECORD - GROUPED BY AGE AND BRAND

 

AGE GROUP: 10-15 YEARS                        TOTAL PATIENTS: 14

Sr. No

Name

Age/Gender

Dose

Suggestion

Brand

1

Pavana S gowda

11/Female

1

Doctor

Gardasil 4

2

Lakshanasri

10/Female

0,2

Self

Gardasil 9

3

Thaniksha

14/Female

0,6

Self

Cervavac

4

Akshana

10/Female

0,6

Self

Cervavac

5

Yazhini

10/Female

0,6

Self

Cervavac

6

Kavinya

10/Female

0,2

Self

Gardasil 9

7

Aaradhya

14/Female

0,2

Self

Gardasil 9

8

Revathi

12/Female

0,2

Self

Gardasil 9

9

Tamilselvi

15/Female

0,2

Self

Gardasil 9

10

Deepasri

11/Female

0,2

Self

Gardasil 9

11

Jeevitha

14/Female

0,6

Self

Gardasil 9

12

Meena

13/Female

0,6

Self

Gardasil 9

13

Vishnupriya

12/Female

0,2

Self

Cervavac

14

Hemalatha

14/Female

0,6

Self

Cervavac

 

AGE GROUP: 16-25 YEARS                              TOTAL PATIENTS: 11

Sr. No.

Name

Age/Gender

Dose

Suggestion

Brand

1

Druthi

25/Female

1,2

Doctor

Gardasil 4

2

Trupthi

16/Female

1

Doctor

Gardasil 9

3

Karparaksha

24/Female

0,2

Self

Gardasil 9

4

Deepanjali

16/Female

0,2

Self

Cervavac

5

Smitha

22/Female

0,2

Self

Cervavac

6

Karparaksha

24/Female

0,2

Self

Gardasil 9

7

Bavya

16/Female

0,6

Self

Gardasil 9

8

Krishika

16/Female

0,2

Self

Gardasil 9

9

Sobiya

22/Female

0,2

Self

Cervavac

10

Roshini

16/Female

0,2

Doctor

Cervavac

11

Ashwini

16/Female

0,2

Self

Cervavac

 

AGE GROUP: 26 YEARS AND ABOV               TOTAL PATIENTS: 13

Sr. No.

Name

Age/Gender

Dose

Suggestion

Brand

1

Pooja

27/Female

1

Self

Gardasil 9

2

Revathi

36/Female

1,2

Doctor

Gardasil 9

3

Priyanka

32/Female

1

Doctor

Gardasil 9

4

Lavanya

30/Female

1,2

Doctor

Gardasil 9

5

Divya G

27/Female

1

Doctor

Gardasil 9

6

Saraswathi

32/Female

1

Self

Gardasil 9

7

Kalavathy

41/Female

1,2

Doctor

Gardasil 9

8

Pusphavathi

41/Female

1,2

Doctor

Gardasil 4

9

Adharsh

27/Male

1

Doctor

Gardasil 9

10

Moksha

35/Female

1

Doctor

Gardasil 4

11

Anitha Princy

30/Female

0,2

Self

Cervavac

12

Megha

27/Female

0,2

Self

Cervavac

13

Santha

27/Female

0,2

Self

Cervavac

 

SUMMARY BY BRAND

Brand

Total Patients

Percentage (%)

Gardasil 9

21

55.3%

Cervavac

13

34.2%

Gardasil 4

4

10.5%

TOTAL

38

100%

The collected data show HPV vaccination among adolescents and adults aged 10–41 years. The records include single-dose and multi-dose schedules, such as 0,2 and 0,6, with vaccines including Gardasil 9, Cervavac, and Gardasil 4. Most vaccinations were recorded among females, with both doctor-recommended and self-initiated vaccination observed.

The data indicate that HPV vaccination is being provided to the recommended adolescent target group as well as adults, highlighting the importance of age-appropriate dosing and adherence to current immunization guidelines.

  • Target population: Primary Target :Girls 9-14 years 

Boys : Recommended for broader protection

Catch-up vaccination: Up to 26 years

Immunocompromised individuals: Up to 45 years

  • Current Immunization Guidelines
  • WHO recommends HPV vaccination for girls ages 9-14 years and considers boys vaccination for wider protection.
  • National immunization programs include HPV vaccine based on disease burden and cost-effectiveness.
  • Use of WHO prequalified vaccines and adherence to cold chain and safety standards.
  • Integration with adolescent health services and school-based vaccination programs.
  • Equity: Ensures access for all eligible populations, especially in low-and middle-income countries Suggestion.

6. To analyze the role of the HPV vaccine in reducing the global burden of cervical cancer and improving public health.

The global burden of HPV remains a major public health concern due to its strong association with cervical cancer and other HPV-related cancers. Increasing HPV vaccination coverage, regular screening, and public awareness can significantly reduce disease burden and prevent cervical cancer worldwide.

7. To identify barriers to HPV vaccination, such as lack of awareness, vaccine hesitancy, and accessibility, and suggest strategies to improve vaccine uptake.

Age Distribution

This table represents the age breakdown of the 39 respondents shown in the bar charts.

Age

Number of Responses

Percentage

18

4

10.3%

19

6

15.4%

20

7

17.9%

21

11

28.2%

22

7

17.9%

23

1

2.6%

25

2

5.1%

29

1

2.6%

Total

39

100%

Gender

This table displays the gender split among the 39 respondents from the pie chart.

Gender

Percentage

Female

64.1%

Male

35.9%

Total

100%

HPV Vaccine Awareness

This table summarises the responses regarding awareness of the HPV vaccine from the second pie chart.

Are you aware of HPV vaccine ?

Percentage

No

51.3%

Yes

48.7%

Total

100%

Vaccine Uptake

Total responses: 39

Answer option

Percentage (%)

Calculated Responses

No

87.2%

34

Yes

12.8%

5

Number of Doses Taken

Total Responses:39

Answer Option

Percentage (%)

Calculated Responses

Nil

87.2%

34

1

7.7%

3

2

5.1%

2

3

0.0.%

0

Vaccine Brand Distribution

Total Responses:39

Answer Option

Percentage (%)

Calculated Responses

Nil

87.2%

34

Cervavac

7.7%

3

Gardasil (4 and 9)

2.6%

1

Cervarix

2.5%

1

Adverse Effects Experienced

Total 39 Responses

Responses

Percentage

Nil (Orange)

79.5%

No (Red)

15.4%

Yes (Blue)

Remaining percentage (approx. 5.1%)

Recommendations

Total 39 responses

Recommendation Category

Percentage

Awareness (Blue)

53.8%

Social media (Orange)

20.5%

Government campaign (Green)

15.4%

Doctor

Remaining percentage (approx. 10.3%)

The findings from Google forms survey indicated that a majority of the respondents had not received the HPV vaccine. This suggests a lack of awareness regarding the importance and benefits of HPV vaccination. The results also indicate that social media has not been sufficiently effective in promoting accurate information and increasing public awareness about the HPV vaccine.

8. To emphasize the importance of pharmacovigilance in monitoring the long-term safety and effectiveness of HPV vaccines after their introduction into immunization programs.

Long-term Safety Monitoring: Pharmacovigilance continuously monitors HPV vaccines after their introduction into immunization programs to identify rare or delayed adverse events, ensuring that the vaccines remain safe for the population.

Assessment of Effectiveness: It evaluates the real-world effectiveness of HPV vaccines in preventing HPV infections and cervical cancer, providing evidence to support public health policies, maintain public confidence, and improve immunization programs.

HPV Vaccine Pharmacovigilance

Section

Key points

Vaccine pharmacovigilance

Systematic detection, assessment, understanding and prevention of adverse events following immunization (AEFIs) associated with HPV vaccines.

Why important for HPV vaccines

HPV vaccines are widely given to adolescents and young adults, who are generally healthy; therefore safety monitoring is important.

1. Common adverse events

Injection-site: pain, redness, swelling

Systemic: headache, fatigue, fever, dizziness Gastrointestinal: nausea

Syncope (fainting): may occur in adolescents; observation for about 15 minutes is commonly recommended.

2. Serious adverse events monitored

Anaphylaxis and severe allergic reactions

Seizures, Guillain–Barré syndrome

Other uncommon or serious events are monitored through pharmacovigilance systems.

3. Signal detection / investigation

Spontaneous-report databases can be assessed using statistical disproportionality methods, followed by epidemiological investigation.

4. Causality assessment

Timing between vaccination and event; biological plausibility; alternative explanations; previous evidence; rechallenge/dechallenge where relevant; epidemiological evidence; background incidence.

Causality framework

WHO AEFI causality-assessment framework can be used to classify the likelihood of vaccine-related causality.

5. Importance in HPV vaccination programs

HPV vaccines have a well-established safety profile, but pharmacovigilance remains important because very rare adverse events may become detectable only after millions of doses.

Pharmacovigilance process

Detection → Reporting → Investigation → Signal detection → Causality assessment → Risk evaluation → Risk minimization → Communication

DISCUSSION

Human Papillomavirus (HPV) infection is one of the most common viral infections and is an important public health concern because certain types of HPV can cause cancer. HPV has many different types, which can be broadly classified as low-risk and high-risk types. Low-risk types such as HPV-6 and HPV-11 are mainly associated with genital warts, while high-risk types such as HPV-16 and HPV-18 are strongly associated with cervical cancer. HPV infection can also contribute to cancers of the anus, penis, vulva, vagina, and oropharynx. Understanding the different types of HPV and how the virus spreads is therefore important for preventing HPV-related diseases.

The HPV vaccine has an important role in preventing HPV infection. It works by stimulating the immune system to produce antibodies against specific HPV types. The vaccine contains Virus-Like Particles (VLPs), which resemble the outer surface of the virus but cannot reproduce or cause infection. These particles help the immune system recognize HPV and respond quickly if a vaccinated person is exposed to the virus later. Therefore, vaccination is mainly preventive and provides the greatest benefit when given before exposure to HPV.

Different HPV vaccine formulations provide protection against different HPV types. Bivalent vaccines protect mainly against HPV-16 and HPV-18, while quadrivalent vaccines provide protection against HPV-6, HPV-11, HPV-16, and HPV-18. The nonavalent vaccine provides broader protection against nine HPV types, including HPV-31, 33, 45, 52, and 58. This wider coverage is particularly useful because several high-risk HPV types can contribute to cancer development.

The effectiveness of HPV vaccination has been demonstrated through clinical studies and population-level evidence. Vaccination significantly reduces HPV infections, precancerous cervical lesions, and other HPV-related diseases. Its greatest public health benefit is the prevention of cervical cancer. However, vaccination does not replace cervical cancer screening. Vaccinated individuals should continue to follow recommended screening programs because the vaccines do not protect against every cancer-causing HPV type.

The safety profile of HPV vaccines has also been an important part . Most adverse events are mild and temporary. Common reactions include pain, redness or swelling at the injection site, headache, fatigue, and mild fever. Fainting can occasionally occur after vaccination, particularly among adolescents, which is why observation for approximately 15 minutes after vaccination is recommended. Serious adverse reactions are rare. Continuous safety monitoring is important to identify any unusual or unexpected events after vaccination.

Pharmacovigilance plays an important role in ensuring the continued safety of HPV vaccines. Safety information is collected and evaluated after vaccines are introduced into the general population. Systems such as VAERS and other national and international monitoring programs help detect possible safety signals. These systems are important because clinical trials, although extensive, may not identify extremely rare adverse events. Pharmacovigilance therefore provides additional information about vaccine safety during large-scale and long-term use.

The recommended HPV vaccination schedule depends on factors such as age and immune status. Vaccination is generally recommended during early adolescence because it provides protection before exposure to HPV is likely to occur. Current immunization recommendations in many settings have also moved toward simplified schedules for younger adolescents. Older individuals and people with certain immune conditions may require additional doses. Following the appropriate vaccination schedule is important for achieving maximum protection.

Although HPV vaccines are highly effective, several barriers can reduce vaccination coverage. Lack of awareness, concerns about vaccine safety, misinformation, parental hesitation, cost, limited healthcare facilities, and difficulty accessing vaccination services can all affect vaccine uptake. Some people may also incorrectly believe that HPV vaccination is unnecessary or that it promotes risky sexual behavior. Providing clear, evidence-based information through healthcare professionals, schools, and public health programs can help address these concerns.

Healthcare professionals, including pharmacists, have an important role in improving HPV vaccine acceptance. Pharmacists can educate patients and parents about the benefits and safety of vaccination, answer questions, address misinformation, encourage completion of recommended vaccination schedules, and support reporting of suspected adverse events. Proper vaccine storage and handling are also important responsibilities in maintaining vaccine quality and effectiveness.

Overall, HPV vaccination is an important preventive strategy for reducing HPV infections and HPV-related cancers, particularly cervical cancer. The combination of early vaccination, appropriate screening, public education, improved accessibility, and continuous pharmacovigilance can significantly contribute to reducing the global burden of HPV-related diseases. Continued monitoring of vaccine safety and effectiveness will also help maintain public confidence and support successful immunization programs.

CONCLUSION

HPV vaccine are safe and effective ways to prevent the Human Papillomavirus which is responsible for reducing the risk of cervical cancer and other HPV related disease . HPV vaccination can provide long-term protection against several related cancers. It works best when given to young adolescents before any exposure to the virus. Taking HPV vaccine is a small step that can make a big difference in protecting our health and the health of future generations. This study improve public knowledge and create awareness about the importance of the HPV vaccination by providing accurate and reliable information about HPV-related disease, to reduce the burden of cervical cancer and contribute to a healthier future for individuals and the community.   

REFERENCES

  1. https://pharmeasy.in/blog/vaccine-human-papillomavirus-hpv-what-is-it-causes-symptoms-and-prevention/
  2. Hager, K. M. (2019). A history of diagnosing HPV. Loading... EBSCO Connect| Privacy policy| Terms of use| Copyright| Manage my cookies Journals| Subjects| Sitemap Software© 2026 EBSCO Industries, LLC. All rights reserved, 51(12), 28] https://share.google/fiS30N2HnRH96h6mu
  3. Wheeler, C. M. (2008). Natural history of human papillomavirus infections, cytologic and histologic abnormalities, and cancer. Obstetrics and gynecology clinics of North America, 35(4), 519-536. https://scholar.google.com/scholar?hl=en&as_sdt=0%2C5&q=history+and+discovery+of+hpv+infection+article+&btnG=#d=gs_qabs&t=1784384105497&u=%23p%3Dx_AM4dCxCiEJ
  4. 4. https://share.google/3AphEbgrO2d6nW5cu
  5. Forman, D., de Martel, C., Lacey, C. J., Soerjomataram, I., Lortet-Tieulent, J., Bruni, L., ... & Franceschi, S. (2012). Global burden of human papillomavirus and related diseases. Vaccine, 30, F12-F23. https://scholar.google.com/scholar?hl=en&as_sdt=0%2C5&q=burden+of+hpv+globally+&oq=gl#d=gs_qabs&t=1785850609957&u=%23p%3DXLZ4Lh1e-9wJ
  6. https://www.mdpi.com/2075-4418/13/2/243
  7. https://www.pib.gov.in/PressReleasePage.aspx?PRID=2233906&reg=3&lang=2
  8. https://www.cdc.gov/hpv/vaccines/index.html
  9. https://www.ncbi.nlm.nih.gov/books/NBK562186/#article-23033.s3
  10. https://www.rgcirc.org/blog/hpv-vaccination-in-india-new-progress-and-the-way-forward/
  11. https://www.mayoclinic.org/diseases-conditions/hpv-infection/in-depth/hpv-vaccine/art-20047292
  12. https://www.researchgate.net/publication/403033374_HPV_Vaccination_Broader_Implementation_and_Development_of_Next-Generation_Vaccines_Reduce_the_Incidence_of_Cervical_Cancer
  13. Beltrame, A., Dube Mandishora, R. S., Wang, W., Fan, W., Haver, M. K., & Giuliano, A. R. (2026). Impact of Male Human Papillomavirus (HPV) Vaccination on HPV Infection and HPV‐Related Diseases: A Systematic Review. Reviews in Medical Virology, 36(4), e70171.
  14. Vasudevan, U., Kelly-Hanku, A., Limbu, P., Jops, P., Shetty, R. S., Gupta, E., ... & Rajbangshi, P. R. (2026). Marginalized voices on HPV vaccination in India: exploring knowledge, attitudes, and acceptance. Frontiers in Global Women's Health, 7, 1791203.
  15. H. Chuwa, A. (2026). Innovations in HPV vaccination and their role in global cervical cancer control: a review. Therapeutic Advances in Vaccines and Immunotherapy, 14, 25151355261449446.
  16. https://pmc.ncbi.nlm.nih.gov/articles/PMC12153397/
  17. Miazga, W., Tatara, T., Gujski, M., Pinkas, J., Ostrowski, J., & Religioni, U. (2025). Global guidelines and trends in HPV vaccination for cervical cancer prevention. Medical Science Monitor: International Medical Journal of Experimental and Clinical Research, 31, e947173.
  18. Shetty, R. S., Nadda, A., Tambe, M., Raut, A., Goel, K., Rao, C. R., ... & Kamath, V. G. (2024). IAPSM’s position paper on the Human Papilloma Virus (HPV) vaccine for adult immunization in India. Indian journal of community medicine: official publication of Indian Association of Preventive & Social Medicine, 49(Suppl 2), S125.  
  19. Lou, P. J., Phongsamart, W., Sukarom, I., Wu, Y. H., Zaidi, O., Du, F., ... & Bernauer, M. (2024). Systematic literature review on the clinical and economic burden of human papillomavirus–related diseases in select areas in the Asia-Pacific region. Human vaccines & immunotherapeutics, 20(1), 2425535.
  20. Goodman, E., Reuschenbach, M., Kaminski, A., & Ronnebaum, S. (2022). Human papillomavirus vaccine impact and effectiveness in six high-risk populations: a systematic literature review. Vaccines, 10(9), 1543
  21. Ellingson, M. K., Sheikha, H., Nyhan, K., Oliveira, C. R., & Niccolai, L. M. (2023). Human papillomavirus vaccine effectiveness by age at vaccination: a systematic review. Human vaccines & immunotherapeutics, 19(2), 2239085.
  22. https://www.lidsen.com/journals/transplantation/transplantation-02-03-017

Reference

  1. https://pharmeasy.in/blog/vaccine-human-papillomavirus-hpv-what-is-it-causes-symptoms-and-prevention/
  2. Hager, K. M. (2019). A history of diagnosing HPV. Loading... EBSCO Connect| Privacy policy| Terms of use| Copyright| Manage my cookies Journals| Subjects| Sitemap Software© 2026 EBSCO Industries, LLC. All rights reserved, 51(12), 28] https://share.google/fiS30N2HnRH96h6mu
  3. Wheeler, C. M. (2008). Natural history of human papillomavirus infections, cytologic and histologic abnormalities, and cancer. Obstetrics and gynecology clinics of North America, 35(4), 519-536. https://scholar.google.com/scholar?hl=en&as_sdt=0%2C5&q=history+and+discovery+of+hpv+infection+article+&btnG=#d=gs_qabs&t=1784384105497&u=%23p%3Dx_AM4dCxCiEJ
  4. 4. https://share.google/3AphEbgrO2d6nW5cu
  5. Forman, D., de Martel, C., Lacey, C. J., Soerjomataram, I., Lortet-Tieulent, J., Bruni, L., ... & Franceschi, S. (2012). Global burden of human papillomavirus and related diseases. Vaccine, 30, F12-F23. https://scholar.google.com/scholar?hl=en&as_sdt=0%2C5&q=burden+of+hpv+globally+&oq=gl#d=gs_qabs&t=1785850609957&u=%23p%3DXLZ4Lh1e-9wJ
  6. https://www.mdpi.com/2075-4418/13/2/243
  7. https://www.pib.gov.in/PressReleasePage.aspx?PRID=2233906&reg=3&lang=2
  8. https://www.cdc.gov/hpv/vaccines/index.html
  9. https://www.ncbi.nlm.nih.gov/books/NBK562186/#article-23033.s3
  10. https://www.rgcirc.org/blog/hpv-vaccination-in-india-new-progress-and-the-way-forward/
  11. https://www.mayoclinic.org/diseases-conditions/hpv-infection/in-depth/hpv-vaccine/art-20047292
  12. https://www.researchgate.net/publication/403033374_HPV_Vaccination_Broader_Implementation_and_Development_of_Next-Generation_Vaccines_Reduce_the_Incidence_of_Cervical_Cancer
  13. Beltrame, A., Dube Mandishora, R. S., Wang, W., Fan, W., Haver, M. K., & Giuliano, A. R. (2026). Impact of Male Human Papillomavirus (HPV) Vaccination on HPV Infection and HPV?Related Diseases: A Systematic Review. Reviews in Medical Virology, 36(4), e70171.
  14. Vasudevan, U., Kelly-Hanku, A., Limbu, P., Jops, P., Shetty, R. S., Gupta, E., ... & Rajbangshi, P. R. (2026). Marginalized voices on HPV vaccination in India: exploring knowledge, attitudes, and acceptance. Frontiers in Global Women's Health, 7, 1791203.
  15. H. Chuwa, A. (2026). Innovations in HPV vaccination and their role in global cervical cancer control: a review. Therapeutic Advances in Vaccines and Immunotherapy, 14, 25151355261449446.
  16. https://pmc.ncbi.nlm.nih.gov/articles/PMC12153397/
  17. Miazga, W., Tatara, T., Gujski, M., Pinkas, J., Ostrowski, J., & Religioni, U. (2025). Global guidelines and trends in HPV vaccination for cervical cancer prevention. Medical Science Monitor: International Medical Journal of Experimental and Clinical Research, 31, e947173.
  18. Shetty, R. S., Nadda, A., Tambe, M., Raut, A., Goel, K., Rao, C. R., ... & Kamath, V. G. (2024). IAPSM’s position paper on the Human Papilloma Virus (HPV) vaccine for adult immunization in India. Indian journal of community medicine: official publication of Indian Association of Preventive & Social Medicine, 49(Suppl 2), S125.  
  19. Lou, P. J., Phongsamart, W., Sukarom, I., Wu, Y. H., Zaidi, O., Du, F., ... & Bernauer, M. (2024). Systematic literature review on the clinical and economic burden of human papillomavirus–related diseases in select areas in the Asia-Pacific region. Human vaccines & immunotherapeutics, 20(1), 2425535.
  20. Goodman, E., Reuschenbach, M., Kaminski, A., & Ronnebaum, S. (2022). Human papillomavirus vaccine impact and effectiveness in six high-risk populations: a systematic literature review. Vaccines, 10(9), 1543
  21. Ellingson, M. K., Sheikha, H., Nyhan, K., Oliveira, C. R., & Niccolai, L. M. (2023). Human papillomavirus vaccine effectiveness by age at vaccination: a systematic review. Human vaccines & immunotherapeutics, 19(2), 2239085.
  22. https://www.lidsen.com/journals/transplantation/transplantation-02-03-017

Photo
Jiji K
Corresponding author

Assistant Professor, Department of Pharmacy Practice, Spurthy College of Pharmacy, Rajiv Gandhi University of Health Sciences, Bengaluru, Karnataka.

Photo
Monisha M
Co-author

Department of Pharmacy Practice, Spurthy College of Pharmacy, Rajiv Gandhi University of Health Sciences, Bengaluru, Karnataka

Photo
B Rashmitha
Co-author

Department of Pharmacy Practice, Spurthy College of Pharmacy, Rajiv Gandhi University of Health Sciences, Bengaluru, Karnataka

Photo
Smitha D
Co-author

Department of Pharmacy Practice, Spurthy College of Pharmacy, Rajiv Gandhi University of Health Sciences, Bengaluru, Karnataka

Photo
Sneha S
Co-author

Department of Pharmacy Practice, Spurthy College of Pharmacy, Rajiv Gandhi University of Health Sciences, Bengaluru, Karnataka

Photo
Swathi S
Co-author

Department of Pharmacy Practice, Spurthy College of Pharmacy, Rajiv Gandhi University of Health Sciences, Bengaluru, Karnataka

B Rashmitha, Monisha M, Smitha D, Sneha S, Swathi S, Jiji K, Evaluation of HPV Vaccine: Safety, Efficacy and Public Health Impact, Int. J. of Pharm. Sci., 2026, Vol 4, Issue 8, 3353-3385. https://doi.org/10.5281/zenodo.22045911

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