Human Papillomavirus (US CDC Pink Book) Patient Information

Human papillomavirus (HPV) is the most common sexually transmitted infection in the United States. The relationship

of cervical cancer and sexual behavior was suspected for more than 100 years and was established by epidemiologic

studies in the 1960s. In the early 1980s, cervical cancer cells were demonstrated to contain HPV DNA. Epidemiologic

studies showing a consistent association between HPV and cervical cancer were published in the 1990s. The first

vaccine to prevent infection with four types of HPV was licensed in 2006.

Human Papillomavirus

Human papillomaviruses are small, double-stranded DNA viruses that infect the epithelium. More than 100 HPV

types have been identified; they are differentiated by the genetic sequence of the outer capsid protein L1. Most HPV

types infect the cutaneous epithelium and cause common skin warts. About 40 types infect the mucosal epithelium;

these are categorized according to their epidemiologic association with cervical cancer. Infection with low-risk,

or nononcogenic types, such as types 6 and 11, can cause benign or low-grade cervical cell abnormalities, genital warts

and laryngeal papillomas. High-risk, or oncogenic, HPV types act as carcinogens in the development of cervical

cancer and other anogenital cancers. High-risk types (currently including types 16, 18, 31, 33, 35, 39, 45, 51, 52,

56, 58, 59, 68, 69, 73, 82) can cause low-grade cervical cell abnormalities, high-grade cervical cell abnormalities that

are precursors to cancer, and anogenital cancers. High-risk HPV types are detected in 99% of cervical cancers. Type 16

is the cause of approximately 50% of cervical cancers worldwide, and types 16 and 18 together account for about 70%

of cervical cancers. Infection with a high-risk HPV type is considered necessary for the development of cervical cancer,

but by itself it is not sufficient to cause cancer because the vast majority of women with HPV infection do not develop


In addition to cervical cancer, HPV infection is also associated with anogenital cancers less common than cervical cancer, such as cancer of the vulva, vagina, penis and anus. The association of genital types of HPV with non-genital cancers is less well established, but studies support a role for these HPV types in a subset of oral cavity and pharyngeal cancers.


HPV infection occurs at the basal epithelium. Although the incidence of infection is high, most infections resolve

spontaneously. A small proportion of infected persons become persistently infected; persistent infection is the most

important risk factor for the development of cervical cancer precursor lesions. The most common clinically significant

manifestation of persistent genital HPV infection is cervical intraepithelial neoplasia, or CIN. Within a few years of

infection, low-grade CIN—called CIN 1—may develop, which may spontaneously resolve and the infection clear.

Persistent HPV infection, however, may progress directly to high-grade CIN, called CIN2 or CIN3. High-grade

abnormalities are at risk of progression to cancer and so are considered cancer precursors. A small proportion of highgrade abnormalities spontaneously regress. If left undetected and untreated, years or decades later CIN2 or 3 can progress to cervical cancer.

Infection with one type of HPV does not prevent infection with another type. Of persons infected with mucosal HPV,

5% to 30% are infected with multiple types of the virus.

Clinical Features

Most HPV infections are asymptomatic and result in no clinical disease. Clinical manifestations of HPV infection

include anogenital warts, recurrent respiratory papillomatosis, cervical cancer precursors (cervical intraepithelial neoplasia), and cancers, including cervical, anal, vaginal, vulvar, penile, and some head and neck cancer.

Laboratory Diagnosis

HPV has not been isolated in culture. Infection is identified by detection of HPV DNA from clinical samples. Assays for

HPV detection differ considerably in their sensitivity and type specificity, and detection is also affected by the anatomic

region sampled as well as the method of specimen collection. Currently, only the Digene Hybrid Capture®2 (hc2) High-

Risk HPV DNA Test is approved by the Food and Drug Administration for clinical use The hc2 uses liquid nucleic

acid hybridization and detects 13 high-risk types (HPV 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 68). Results are

reported as positive or negative and are not type-specific. The hc2 test is approved for triage of women with equivocal

Papanicolaou (Pap) test results (ASC-US, atypical cells of undetermined significance) and in combination with the

Pap test for cervical cancer screening in women over age 30. The test is not clinically indicated nor approved for use in men.

Epidemiologic and basic research studies of HPV generally use nucleic acid amplification methods that generate typespecific results. The PCR assays used most commonly in epidemiologic studies target genetically conserved regions in the L1 gene.

The most frequently used HPV serologic assays are VLPbased enzyme immunoassays. However, laboratory reagents

used for these assays are not standardized and there are no standards for setting a threshold for a positive result.

Medical Management

There is no specific treatment for HPV infection. Medical management depends on treatment of the specific clinical

manifestation of the infection (such as genital warts or abnormal cervical cell cytology).



HPV infection occurs throughout the world.


Viruses in the papillomavirus family affect other species (notably rabbits and cows). However, humans are the only

natural reservoir of HPV.


HPV is transmitted by direct contact, usually sexual, with an infected person. Transmission occurs most frequently

with sexual intercourse but can occur following nonpenetrative sexual activity. Studies of newly acquired HPV infection demonstrate that infection occurs soon after onset of sexual activity. In a prospective study of college women, the cumulative incidence of infection was 40% by 24 months after first sexual intercourse. HPV 16 accounted for 10.4% of infections.

Genital HPV infection also may be transmitted by nonsexual routes, but this appears to be uncommon. Nonsexual

routes of genital HPV transmission include transmission from a woman to a newborn infant at the time of birth.

Temporal Pattern

There is no known seasonal variation in HPV infection.


HPV is presumably communicable during the acute infection and during persistent infection. This issue is difficult to

study because of the inability to culture the virus. Communicability can presumed to be high because of the

large number of new infections estimated to occur each year.

Risk Factors

Risk factors for HPV infection are related to sexual behavior, including the number of sex partners, lifetime history of

sex partners, and the partners’ sexual history. Most studies suggest that young age (less than 25 years) is a risk factor

for infection. Results of epidemiologic studies are less consistent for other risk factors, including young age at sexual

initiation, inconsistent condom use, number of pregnancies, genetic factors, smoking, lack of circumcision of male partner, and oral contraceptive use

Disease Burden in the United States

Anogenital HPV infection is
believed to be the most common sexually transmitted infection in the United States. An

estimated 20 million persons are currently infected, and an estimated 6.2 million new HPV infections occur annually.

HPV infection is common among adolescents and young adults. Prevalence among adolescent girls is as high as 64%.

Up to 75% of new infections occur among persons 15–24 years of age. Modeling estimates suggest that more than 80%

of sexually active women will have been infected by age 50.

HPV infection is also common in men. Among heterosexual men in clinic-based studies, prevalence of genital HPV

infection is often greater than 20%. Prevalence is highly dependent on the anatomic sites sampled and method of

specimen collection.

The two most common types of cervical cancer worldwide, squamous cell carcinoma followed by adenocarcinoma, are

both caused by HPV. The American Cancer Society estimates that in 2006 about 9,700 new cases of cervical cancer

will be diagnosed in the United States. Approximately 3,700 women will die as a result of cervical cancer. HPV is

believed to be responsible for nearly all of these cases of cervical cancer. HPV types 16 and 18 are associated with

70% of these cancers.

In addition to cervical cancer, HPV is believed to be responsible for 90% of anal cancers, 40% of vulvar, vaginal,

or penile cancers, and 12% of oral and pharyngeal cancers. Population-based estimates, primarily from clinics treating

persons with sexually transmitted infections, indicate that about 1% of the sexually active adolescent and adult population in the United States have clinically apparent genital warts. More than 90% of cases of anogenital warts are associated with the low-risk HPV types 6 and 11.

About 4 billion dollars are spent annually on management of sequelae of HPV infections, primarily for the management

of abnormal cervical cytology and treatment of cervical neoplasia. This exceeds the economic burden of any other

sexually transmitted infection except human immunodeficiency virus.


HPV Infection

HPV transmission can be reduced but not eliminated with the use of physical barriers such as condoms. Recent studies

demonstrated a significant reduction in HPV infection among young women after initiation of sexual activity when

their partners used condoms consistently and correctly.

Abstaining from sexual activity (i.e., refraining from any genital contact with another individual) is the surest way to

prevent genital HPV infection. For those who choose to be sexually active, a monogamous relationship with an uninfected partner is the strategy most likely to prevent future genital HPV infections.

Cervical Cancer Screening

Most cases and deaths from cervical cancer can be prevented through detection of precancerous changes

within the cervix by cervical cytology using the Pap test.

Currently available Pap test screening can be done by a conventional Pap or a liquid-based cytology. CDC does

not issue recommendations for cervical cancer screening, but various professional groups have published recommendations.

The American College of Obstetricians and Gynecologists (ACOG), the American Cancer Society

(ACS), and the U.S. Preventive Services Task Force (USPSTF) guidelines recommend that all women should

have a Pap test for cervical cancer screening within 3 years of beginning sexual activity or by age 21, whichever

occurs first. While the USPSTF recommends a conventional Pap test at least every 3 years regardless of age, ACS

and ACOG recommend annual or biennial screening of women younger than age 30, depending on use of

conventional or liquid–based cytology. According to these national organizations, women over age 30 with three

normal consecutive Pap tests should be screened every 2 to 3 years.

The use of HPV vaccine does not eliminate the need for continued Pap test screening, since 30% of cervical cancers

are caused by HPV types not included in the vaccine.

Human Papillomavirus Vaccine


The currently licensed vaccine is a quadrivalent HPV vaccine (Gardasil, Merck). The vaccine antigen is the L1

major capsid protein of HPV, produced by using recombinant DNA technology. The L1 protein is expressed

in Saccharomyces cerevisiae (yeast) cells, and the protein self-assembles into noninfectious, nononcogenic viruslike-

particles (VLP). Each 0.5-mL dose contains 20 μg HPV 6 L1 protein, 40 μg HPV 11 L1 protein, 40 μg HPV

16 L1 protein, and 20 μg HPV 18 L1 protein. The VLPs are adsorbed on 225 μg alum adjuvant. The vaccine also

includes sodium chloride, L-histidine, polysorbate 80, sodium borate, and water for injection. The quadrivalent

HPV vaccine contains no thimerosal or antibiotics. The vaccine is supplied in single-dose vials and syringes.

Immunogenicity and Vaccine Efficacy

The immunogenicity of the quadrivalent HPV vaccine has been measured by detection of IgG antibody to the HPV L1

by a type-specific immunoassay developed by the manufacturer.

In all studies conducted to date, more than 99.5% of participants developed an antibody response to all four

HPV types in the vaccine 1 month after completing the three-dose series. At that time interval, antibody titers against

HPV types 6, 11, 16, and 18 were higher than those that developed after natural HPV infection.

There is no known serologic correlative of immunity and no known minimal titer determined to be protective. The high

efficacy found in the clinical trials to date has precluded identification of a minimum protective antibody titer. Further

follow-up of vaccinated cohorts may allow determination of serologic correlates of immunity in the future.

HPV vaccine has been found to have high efficacy for prevention of HPV vaccine type–related persistent infection,

vaccine type–related CIN, CIN2/3, and external genital lesions in women 16–26 years of age. Clinical efficacy

against cervical disease was determined in two double-blind, placebo-controlled trials, using various endpoints. Vaccine

efficacy was 100% for prevention of HPV 16 or 18–related CIN 2/3 or adenocarcinoma in-situ (AIS). Efficacy against

any CIN due to HPV 6, 11, 16, or 18 was 95%. Efficacy against HPV 6, 11, 16 or 18–related genital warts was 99%.

Although high efficacy among females without evidence of infection with vaccine HPV types was demonstrated in

clinical trials, there was no evidence of efficacy against disease caused by vaccine types with which participants were

infected at the time of vaccination. Participants infected with one or more vaccine HPV types prior to vaccination

were protected against disease caused by the other vaccine types. However, prior infection with one HPV type did not

diminish efficacy of the vaccine against other vaccine HPV types.

There is no evidence that the vaccine protects against disease due to non-vaccine HPV types or provides a therapeutic

effect against cervical disease or genital warts present at the time of vaccination.

A subset of participants in the phase II HPV vaccine study has been followed for 60 months post-dose 1 with no evidence

of waning protection. Study populations will continue to be followed for any evidence of waning immunity.

HPV vaccine has been shown to be immunogenic and safe in males. However, no clinical efficacy data are available for

males. These studies are in progress.

Vaccination Schedule and Use

As of January 2007, ACIP recommendations for use of HPV vaccine have not been published. Recommendations included
here are provisional until published in the Morbidity and Mortality Weekly Report.

Quadrivalent HPV vaccine is licensed by the Food and Drug Administration for use among females 9–26 years of

age. The recommended age for routine vaccination in the United States is 11–12 years. The vaccine can be given as

young as 9 years of age at the discretion of the clinician.

The vaccine should be given at the same visit as other vaccines recommended for persons of this age (e.g., Tdap,

meningococcal conjugate, hepatitis B).

At the beginning of a vaccination program, there will be females older than 12 years of age who did not have the

opportunity to receive vaccine at age 11–12 years. Catch-up vaccination is recommended for females 13 through 26 years of age who have not been previously vaccinated or who have not completed the full series. Ideally, vaccine should

be administered before potential exposure to HPV through sexual contact; however, females who may have already

been exposed to HPV should be vaccinated. Sexually active females who have not been infected with any of the HPV

vaccine types will receive full benefit from vaccination.

Vaccination will provide less benefit to females if they have already been infected with one or more of the four HPV

vaccine types. However, it is not possible for a clinician to assess the extent to which sexually active females would

benefit from vaccination, and the risk of HPV infection may continue as long as persons are sexually active. Pap testing

or screening for HPV DNA or HPV antibody is not recommended prior to vaccination at any age.

HPV vaccine is administered in a three-dose series administered by intramuscular injection. The second and third

doses should be administered 2 and 6 months after the first dose. The minimum interval between the first and second

doses is 4 weeks. The minimum interval between the second and third dose of vaccine is 12 weeks. Doses administered at an interval shorter than the minimum interval should not be counted as valid and should be repeated.

If the HPV vaccine schedule is interrupted, the vaccine series does not need to be restarted. If the series is interrupted

after the first dose, the second dose should be given as soon as possible, and the second and third doses should be

separated by an interval of at least 12 weeks. If only the third dose is delayed, it should be administered as soon as possible.

Although no data are available yet on administration of quadrivalent HPV vaccine with vaccines other than

hepatitis B vaccine, the vaccine contains only HPV capsid protein and has no components that have been found to

adversely affect safety or efficacy of other vaccinations.

The vaccine can be administered at the same visit as other age-appropriate vaccines, such as Tdap and quadrivalent

meningococcal conjugate (MCV4) vaccines. Administering all indicated vaccines at a single visit increases the likelihood

that adolescents and young adults will receive each of the vaccines on schedule. Each vaccine should be administered

using a separate syringe at a different anatomic site.

HPV vaccine is not approved for use among females younger than 9 years or older than 26 years of age. Use of the vaccine in females younger than 9 years or older than 26 years is not recommended. Studies with females older than 26 years of age are ongoing. There are no current studies among children younger than 9 years of age.

Quadrivalent HPV vaccine is not licensed for use among males, and off-label use among males is not recommended.

While data on immunogenicity and safety are available for 9–15-year-old males, there are no data on efficacy in males

at any age. Efficacy studies among males are under way.

Females who have an equivocal or abnormal Pap test could be infected with any of more than 40 high-risk or low-risk

genital HPV types. It is unlikely that such females would be infected with all four HPV vaccine types, and they may not

be infected with any HPV vaccine type. Women younger than 27 years with a previously abnormal Pap test may be

vaccinated. Women should be advised that data do not indicate the vaccine will have any therapeutic effect on

existing HPV infection or cervical lesions.

Females who have a positive HPV DNA test (Hybrid Capture 2®)done in conjunction with a Pap test could be infected with any of 13 high-risk types. This assay does not identify specific HPV types, and testing for specific HPV types is not done routinely in clinical practice. Women younger than 27 years with a positive HPV DNA test may be vaccinated. HPV DNA testing is not a prerequisite for vaccination. Women should be advised that the vaccine will not have a therapeutic effect on existing HPV infection or cervical lesions. A history of genital warts or clinically evident genital warts indicate infection with HPV, most often type 6 or 11. However, these females may be infected with HPV types other than the vaccine types, and therefore they may receive HPV vaccine if they are in the recommended age group. Women with a history of genital warts should be advised that data do not indicate the vaccine will have any therapeutic effect on existing HPV infection or genital warts.

Because quadrivalent HPV vaccine is a subunit vaccine, it can be administered to females who are immunosuppressed

because of disease or medications. However, the immune response and vaccine efficacy might be less than that in

persons who are immunocompetent. Women who are breastfeeding may receive HPV vaccine.

Adverse Reactions Following


The most common adverse reactions reported during clinical trials of HPV vaccine were local reactions at the site of

injection. These were most commonly pain (84%), swelling (25%), and erythema (25%). The majority of injection-site

adverse experiences reported by recipients of quadrivalent HPV vaccine were mild to moderate in intensity. Fever was

reported within 15 days of vaccination by 10% of vaccine recipients and 9% of placebo recipients. No serious adverse

reactions have been reported.

A variety of systemic adverse reactions were reported by vaccine recipients, including nausea, dizziness, myalgia and

malaise. However, these symptoms occurred with equal frequency among both vaccine and placebo recipients.

Contraindications and Precautions

to Vaccination

A severe allergic reaction (acute respiratory distress or collapse) to a vaccine component or following a prior dose

of HPV vaccine is a contraindication to receipt of HPV vaccine. A moderate or severe acute illness is a precaution

to vaccination, and vaccination should be deferred until symptoms of the acute illness improve. A minor acute illness

(e.g., diarrhea or mild upper respiratory tract infection, with or without fever) is not a reason to defer vaccination.

HPV vaccine is not recommended for use during pregnancy. The vaccine has not been associated with adverse outcomes

of pregnancy or with adverse effects on the developing fetus. However, data on vaccination during pregnancy are limited.

Until further information is available, initiation of the vaccine series should be delayed until after completion of

the pregnancy. If a woman is found to be pregnant after initiating the vaccination series, the remainder of the threedose regimen should be delayed until after completion of the pregnancy. If a vaccine dose has been administered during pregnancy, no intervention is indicated. A vaccine in pregnancy registry has been established; patients and healthcare providers are urged to report any exposure to quadrivalent

HPV vaccine during pregnancy by calling (800) 986-8999.

Vaccine Storage and H


HPV vaccine should be stored continuously at 35°–46°F (2°–8°C) and should be protected from light. The vaccine

should be removed from refrigeration immediately before administration. The vaccine must not be exposed to freezing

temperature. Vaccine exposed to freezing temperature should never be administered.

Selected References

American College of Obstetricians and Gynecologists.  Human papillomavirus vaccination. ACOG committee opinion No. 344. Obstet Gynecol 2006;108:699–705.

CDC. Provisional recommendations for the use of quadrivalent HPV vaccine. Available at http://www.cdc.

gov/nip/recs/provisional_recs/hpv.pdf (Publication of these recommendations is anticipated in early 2007.)

Dunne E, Markowitz L. Genital human papillomavirus infection. Clin Infect Dis 2006;43:624–9.

Koutsky LA, Kiviat NB. Genital human papillomavirus. In: Holmes KK, Sparling PF, Mardh PA, et al, eds. Sexually

Transmitted Diseases. 3rd ed. New York: McGraw-Hill; 1999:347–59.

Schiller J, Lowy D. Human papillomavirus vaccines for cervical cancer prevention. In: Plotkin SA, Orenstein, WA,

eds. Vaccines. 4th ed. Philadelphia: Saunders; 2003:1259–65.

Trottier H, Franco E. The epidemiology of genital human papillomavirus infection. Vaccine 2006;24(suppl1):51–15.

Parkin DM. The global health burden of infection-associated cancers in the year 2002. Int J Cancer. 2006;118:3030–44

Weinstock H, Berman S, Cates W, Jr. Sexually transmitted diseases among American youth: incidence and prevalence

estimates, 2000. Perspect Sex Reprod Health. 2004;36:6–10.

Winer R, Hughes J, Feng Q, et al. Condom use and the risk of genital human papillomavirus infection in young women.

N Engl J Med 2006;354:2645–54.

Winer R, Lee S, Hughes J, et al. Genital human papillomavirus infection incidence and risk factors in a cohort of

female university students. Am J Epidemiol 2003;157:218-26.


發佈留言必須填寫的電子郵件地址不會公開。 必填欄位標示為 *