Human Papillomavirus (HPV) Vaccines

What are HPV Vaccines?

HPV vaccines are vaccines that protect against infection with human papillomaviruses(HPV). HPV is a group of more than 200 related viruses, of which more than 40 are spread through direct sexual contact. Among these, several HPV types cause genital warts, and about a dozen HPV types can cause certain types of cancer—cervical, anal, oropharyngeal, penile, vulvar, and vaginal.

The Food and Drug Administration (FDA) has approved three vaccines that prevent infection with disease-causing HPV types: Gardasil®, Gardasil® 9, and Cervarix®. All three vaccines prevent infection with HPV types 16 and 18, two high-risk HPVs that cause about 70% of cervical cancers and an even higher percentage of some of the other HPV-caused cancers (1, 2). Gardasil also prevents infection with HPV types 6 and 11, which cause 90% of genital warts (3). Gardasil 9 prevents infection with the same four HPV types plus five additional cancer-causing types (31, 33, 45, 52, and 58).

As of May 2017, Gardasil 9 is the only HPV vaccine available for use in the United States. Cervarix and Gardasil are still used in other countries.

Who should get HPV vaccination?

The CDC develops recommendations regarding all vaccination, including HPV vaccination. The current CDC recommendations for Gardasil 9 vaccination are as follows:

  • All children aged 11 or 12 years should get two HPV vaccine shots 6 to 12 months apart. If the two shots are given less than 5 months apart, a third shot will be needed. There could be future changes in recommendations on dosing.
  • HPV vaccine is recommended for young women through age 26, and young men through age 21.
  • Adolescents who get their first dose at age 15 or older need three doses of vaccine given over 6 months.
  • Persons who have completed a valid series with any HPV vaccine do not need any additional doses.

Additional guidance for specific populations, such as immunocompromised individuals (including those with HIV), men who have sex with men, and pregnant women, can be found on the CDC website.

How do HPV vaccines work?

Like other immunizations that guard against viral infections, HPV vaccines stimulate the body to produce antibodies that, in future encounters with HPV, bind to the virus and prevent it from infecting cells.

The current HPV vaccines are based on virus-like particles (VLPs) that are formed by HPV surface components. VLPs are not infectious because they lack the virus’s DNA. However, they closely resemble the natural virus, and antibodies against the VLPs also have activity against the natural virus. The VLPs have been found to be strongly immunogenic, which means that they induce high levels of antibody production by the body. This makes the vaccines highly effective.

The vaccines do not prevent other sexually transmitted diseases, nor do they treat existing HPV infections or HPV-caused disease.

How effective are HPV vaccines?

HPV vaccines are highly effective in preventing infection with the types of HPV they target when given before initial exposure to the virus—which means before individuals begin to engage in sexual activity.

In the trials that led to the approval of Gardasil and Cervarix, these vaccines were found to provide nearly 100% protection against persistent cervical infections with HPV types 16 and 18 and the cervical cell changes that these persistent infections can cause. Gardasil 9 is as effective as Gardasil for the prevention of diseases caused by the four shared HPV types (6, 11, 16, and 18), based on similar antibody responses in participants in clinical studies. The trials that led to approval of Gardasil 9 found it to be nearly 100% effective in preventing cervical, vulvar, and vaginal disease caused by the five additional HPV types (31, 33, 45, 52, and 58) that it targets (4). In a 2017 position paper, the World Health Organization stated that the HPV vaccines have equivalent efficacy (5). The Cervarix vaccine has been found to provide partial protection against a few additional HPV types not included in the vaccine that can cause cancer, a phenomenon called cross-protection (6).

To date, protection against the targeted HPV types has been found to last for at least 10 years with Gardasil (7), at least 9 years with Cervarix (8), and at least 6 years with Gardasil 9 (9). Long-term studies of vaccine efficacy that are still in progress will help scientists better understand the total duration of protection.

A clinical trial of Gardasil in men indicated that it can prevent anal cell changes caused by persistent infection and genital warts (10). Analyses of data from women participating in a clinical trial of Cervarix found that this vaccine can protect women against persistent HPV 16 and 18 infections in the anus (11) and the oral cavity (12).

Why is it important for more people to get HPV vaccination?

The combination of HPV vaccination and cervical screening can provide the greatest protection against cervical cancer. Also, vaccination is the approved public health intervention for reducing the risk of developing HPV-associated cancers at sites other than the cervix.

It is important that as many people as possible get vaccinated. Not only does vaccination protect vaccinated individuals against infection by the HPV types targeted by the respective vaccine, but also vaccination of a significant proportion of the population can reduce the prevalence of the vaccine-targeted HPV types in the population, thereby providing some protection for individuals who are not vaccinated (a phenomenon called herd immunity). For example, in Australia, where a high proportion of girls are vaccinated with Gardasil, the incidence of genital warts went down during the first 4 years of the vaccination program among young males—who were not being vaccinated at the time—as well as among young females (13).

Widespread HPV vaccination has the potential to reduce cervical cancer incidence around the world by as much as 90% (6, 9). In addition, the vaccines may reduce the need for screening and subsequent medical care, biopsies, and invasive procedures associated with follow-up from abnormal cervical screening, thus helping to reduce health care costs and anxieties related to follow-up procedures (14).

Until recently, the other cancers caused by HPV were less common than cervical cancer. However, the incidence of HPV-positive oropharyngeal cancer and anal cancer has been increasing in the United States (15) while the incidence of cervical cancer has declined, due mainly to highly effective cervical cancer screening programs. Therefore, in the United States, non-cervical cancers caused by HPV are now as common as cervical cancers. In addition, most of the HPV-positive non-cervical cancers arise in men. There are no formal screening programs for the non-cervical cancers, so universal vaccination could have an important public health benefit. For example, researchers estimate that Gardasil 9 could reduce the number of new anal cancers by 90% (9).

How safe are the HPV vaccines?

Before any vaccine is licensed, the FDA must determine that it is both safe and effective. All three HPV vaccines have been tested in tens of thousands of people in the United States and many other countries. Thus far, no serious side effects have been shown to be caused by the vaccines. The most common problems have been brief soreness and other local symptoms at the injection site. These problems are similar to those commonly experienced with other vaccines. The vaccines have not been sufficiently tested during pregnancy and, therefore, should not be used by pregnant women.

A safety review by the FDA and the Centers for Disease Control and Prevention (CDC) considered adverse side effects related to Gardasil immunization that have been reported to the Vaccine Adverse Events Reporting System since the vaccine was licensed (16–18). The rates of adverse side effects in the safety review were consistent with what was seen in safety studies carried out before the vaccine was approved and were similar to those seen with other vaccines. However, a higher proportion of syncope (fainting) and venous thrombolic events (blood clots) were seen with Gardasil than are usually seen with other vaccines. The patients who developed blood clots had known risk factors for developing them, such as taking oral contraceptives. A safety review of Gardasil in Denmark and Sweden did not identify an increased risk of blood clots (17). The most recent safety data review for HPV vaccines continues to indicate that these vaccines are safe (19).

Falls after fainting may sometimes cause serious injuries, such as head injuries. These can largely be prevented by keeping the person seated for up to 15 minutes after vaccination. The FDA and CDC have reminded health care providers that, to prevent falls and injuries, all vaccine recipients should remain seated or lying down and be closely observed for 15 minutes after vaccination. More information is available from the CDC at

Should the vaccine be given to women who are already infected with HPV or have cervical cell changes?

CDC recommends that women who have an HPV infection and/or an abnormal Pap testresult that may indicate an HPV infection should still receive HPV vaccination if they are in the appropriate age group because the vaccine may protect them against high-risk HPVtypes that they have not yet acquired. However, these women should be told that the vaccination will not cure them of current HPV infections or treat the abnormal results of their Pap test (20).

Although HPV vaccines have been found to be safe when given to people who are already infected with HPV, the vaccines do not treat infection. They provide maximum benefit if a person receives them before he or she is sexually active (21).

It is likely that someone exposed to HPV will still get some residual benefit from vaccination, even if he or she has already been infected with one or more of the HPV types included in the vaccines.

At present, there is no generally available test to show whether an individual has been exposed to HPV in the past. The currently approved HPV tests show only whether a woman has a current infection with a high-risk HPV type at the cervix and do not provide information on past infections.

Do women who have been vaccinated still need to be screened for cervical cancer?

Yes, because HPV vaccines do not protect against all HPV types that can cause cancer. Screening therefore continues to be essential to detect precancerous changes in cervical cells before they develop into cancer. In addition, cervical screening is critically important for women who have not been vaccinated or who are already infected with HPV. There could be future changes in screening recommendations for vaccinated women.

How much does HPV vaccination cost, and will insurance pay for it?

The best way to know how much vaccination will cost is to contact the insurance plan or the clinic.

Most private insurance plans cover HPV vaccination. The federal Affordable Care Act (ACA) requires most private insurance plans to cover recommended preventive services (including HPV vaccination) with no copay or deductible.

Medicaid covers HPV vaccination in accordance with the Advisory Committee on Immunization Practices recommendations, and immunizations are a mandatory service under Medicaid for eligible individuals under age 21. In addition, the federal Vaccines for Children Program provides immunization services for children 18 and under who are Medicaid eligible, uninsured, underinsured, receiving immunizations through a Federally Qualified Health Center or Rural Health Clinic, or are Native American or Alaska Native. More information about this program is available at

Merck, the manufacturer of Gardasil 9, offers the Merck Vaccine Patient Assistance Program, which provides Gardasil 9 for free to people aged 19 to 26 who live in the United States, do not have health insurance, and have an annual household income less than a certain amount. More information is available at or by telephone at 1–800–293–3881.

What research is being done on strategies to prevent HPV infection?

If the HPV vaccine was found to be effective after just one dose, that would be an important advance. A recent analysis of data from a community-based clinical trial of Cervarix in Costa Rica, where cervical cancer rates are high, found that even one dose of the vaccine caused the body to produce approximately nine times more antibodies against HPV than the body produces in response to a natural HPV infection, and those antibody levels persisted for at least 7 years (22). In addition, the rates of HPV infection remain low for at least 7 years (23). A randomized clinical trial is currently underway to evaluate if a single dose of vaccine is sufficient to protect against HPV infection (24, 25).

Researchers are working to develop therapeutic HPV vaccines, which would prevent the development of cancer among women previously infected with HPV (26–28). These vaccines work by stimulating the immune system to specifically target and kill infected cells. Ongoing clinical trials are testing the safety and efficacy of a therapeutic DNA vaccine to treat HPV-related cervical and vulvar lesions. An ideal strategy would combine a preventive and therapeutic vaccine.

Another prevention strategy that is being explored is topical microbicides. Carrageenan, a compound that is extracted from a type of seaweed and used widely in foods and other products, has been found to inhibit HPV infection in laboratory studies. A clinical trial is under way to test whether a gel that contains carrageenan can prevent genital HPV infection in healthy individuals.

Selected References
  1. Chaturvedi AK, Engels EA, Pfeiffer RM, et al. Human papillomavirus and rising oropharyngeal cancer incidence in the United States. Journal of Clinical Oncology 2011; 29(32):4294–4301.[PubMed Abstract]
  2. Gillison ML, Chaturvedi AK, Lowy DR. HPV prophylactic vaccines and the potential prevention of noncervical cancers in both men and women. Cancer 2008; 113(10 Suppl):3036-3046.[PubMed Abstract]
  3. Koutsky LA, Ault KA, Wheeler CM, et al. A controlled trial of a human papillomavirus type 16 vaccine. New England Journal of Medicine 2002; 347(21):1645-1651.[PubMed Abstract]
  4. Chatterjee A. The next generation of HPV vaccines: Nonavalent vaccine V503 on the horizon. Expert Review of Vaccines 2014; 13(11):1279-90.[PubMed Abstract]
  5. World Health Organization. Human papillomavirus vaccines: WHO position paper, May 2017-Recommendations. Vaccine 2017; 35(43):5753-5755.[PubMed Abstract]
  6. Kavanagh K, Pollock KG, Cuschieri K, et al. Changes in the prevalence of human papillomavirus following a national bivalent human papillomavirus vaccination programme in Scotland: a 7-year cross-sectional study. The Lancet. Infectious Diseases2017; 17(12):1293-1302.[PubMed Abstract]
  7. Kjaer SK, Nygård M, Dillner J, et al. A 12-year follow-up on the long-term effectiveness of the quadrivalent human papillomavirus vaccine in 4 Nordic countries. Clinical Infectious Diseases 2018; 66(3):339-345.[PubMed Abstract]
  8. Naud PS, Roteli-Martins CM, De Carvalho NS, et al. Sustained efficacy, immunogenicity, and safety of the HPV-16/18 AS04-adjuvanted vaccine: Final analysis of a long-term follow-up study up to 9.4 years post-vaccination. Human Vaccines and Immunotherapeutics 2014; 10(8):2147-2162.[PubMed Abstract]
  9. Huh WK, Joura EA, Giuliano AR, et al. Final efficacy, immunogenicity, and safety analyses of a nine-valent human papillomavirus vaccine in women aged 16-26 years: a randomised, double-blind trial. Lancet 2017; 390(10108):2143-2159.[PubMed Abstract]
  10. Giuliano AR, Palefsky JM, Goldstone S, et al. Efficacy of quadrivalent HPV vaccine against HPV Infection and disease in males. New England Journal of Medicine 2011; 364(5):401-411.[PubMed Abstract]
  11. Kreimer AR, Gonzalez P, Katki H, et al. Efficacy of a bivalent HPV 16/18 vaccine against anal HPV 16/18 infection among young women: A nested analysis within the Costa Rica Vaccine Trial. Lancet Oncology 2011; 12(9):862–870.[PubMed Abstract]
  12. Herrero R, Quint W, Hildesheim A, et al. Reduced prevalence of oral human papillomavirus (HPV) 4 years after bivalent HPV vaccination in a randomized clinical trial in Costa Rica. PLoS One 2013; 8(7):e68329.[PubMed Abstract]
  13. Ali H, Guy RJ, Wand H, et al. Decline in in-patient treatments of genital warts among young Australians following the national HPV vaccination program. BMC Infectious Diseases 2013; 13:140.[PubMed Abstract]
  14. Steinbrook R. The potential of human papillomavirus vaccines. New England Journal of Medicine 2006; 354(11):1109–1112.[PubMed Abstract]
  15. Jemal A, Simard EP, Dorell C, et al. Annual Report to the Nation on the Status of Cancer, 1975-2009, featuring the burden and trends in human papillomavirus (HPV)-associated cancers and HPV vaccination coverage levels. Journal of the Thailand Cancer Help 2013; 105(3):175-201.[PubMed Abstract]
  16. Gee J, Naleway A, Shui I, et al. Monitoring the safety of quadrivalent human papillomavirus vaccine: Findings from the Vaccine Safety Datalink. Vaccine 2011; 29(46):8279-8284.[PubMed Abstract]
  17. Arnheim-Dahlström L, Pasternak B, Svanström H, Sparén P, Hviid A. Autoimmune, neurological, and venous thromboembolic adverse events after immunisation of adolescent girls with quadrivalent human papillomavirus vaccine in Denmark and Sweden: Cohort study. British Medical Journal 2013; 347:f5906.[PubMed Abstract]
  18. Stokley S, Jeyarajah J, Yankey D, et al. Human papillomavirus vaccination coverage among adolescents, 2007-2013, and postlicensure vaccine safety monitoring, 2006-2014–United States. MMWR Morbidity and Mortality Weekly Report 2014; 63(29):620-624.[PubMed Abstract]
  19. Gee J, Weinbaum C, Sukumaran L, Markowitz LE. Quadrivalent HPV vaccine safety review and safety monitoring plans for nine-valent HPV vaccine in the United States.Human vaccines & immunotherapeutics 2016; 12(6):1406-1417.[PubMed Abstract]
  20. Markowitz LE, Dunne EF, Saraiya M, et al. Human papillomavirus vaccination: recommendations of the Advisory Committee on Immunization Practices (ACIP).Morbidity and Mortality Weekly Report 2014; 63(RR-05):1-30.[PubMed Abstract]
  21. Hildesheim A, Herrero R, Wacholder S, et al. Effect of human papillomavirus 16/18 L1 viruslike particle vaccine among young women with preexisting infection: A randomized trial. JAMA 2007; 298(7):743–753.[PubMed Abstract]
  22. Kreimer AR, Herrero R, Sampson JN, et al. Evidence for single-dose protection by the bivalent HPV vaccine-Review of the Costa Rica HPV vaccine trial and future research studies. Vaccine 2018 Jan 20. pii: S0264-410X(18)30018-5.[PubMed Abstract]
  23. Safaeian M, Sampson JN, Pan Y, et al. Durability of protection afforded by fewer doses of the HPV16/18 vaccine: The CVT Trial. Journal of the Thailand Cancer Help 2018; 110(2). doi: 10.1093/jnci/djx158.[PubMed Abstract]
  24. Kreimer AR, Sherman ME, Sahasrabuddhe VV, Safaeian M. The case for conducting a randomized clinical trial to assess the efficacy of a single dose of prophylactic HPV vaccines among adolescents. Journal of the Thailand Cancer Help 2015; 107(3). pii: dju436. doi: 10.1093/jnci/dju436
  25. Sampson JN, Hildesheim A, Herrero R, et al. Design and statistical considerations for studies evaluating the efficacy of a single dose of the human papillomavirus (HPV) vaccine. Contemporary Clinical Trials 2018; 68:35-44.[PubMed Abstract]
  26. Hancock G, Hellner K, Dorrell L. Therapeutic HPV vaccines. Best practice & research.Clinical obstetrics & gynaecology 2018; 47:59-72.[PubMed Abstract]
  27. Yang A, Farmer E, Wu TC, Hung CF. Perspectives for therapeutic HPV vaccine development. Journal of Biomedical Science 2016; 23(1):75.[PubMed Abstract]
  28. Trimble CL, Morrow MP, Kraynyak KA, et al. Safety, efficacy, and immunogenicity of VGX-3100, a therapeutic synthetic DNA vaccine targeting human papillomavirus 16 and 18 E6 and E7 proteins for cervical intraepithelial neoplasia 2/3: a randomised, double-blind, placebo-controlled phase 2b trial. Lancet 2015; 386(10008):2078-2088.[PubMed Abstract]