An HPV infection is caused by thehuman papillomavirus, a DNA virus from the papillomavirus family.[8][9] Over 200 types have been described.[10][11] An individual can become infected with more than one type of HPV,[12] and the disease is only known to affect humans.[5][13] More than 40 types may bespread through sexual contact and infect theanus andgenitals.[4] Risk factors for persistent infection by sexually transmitted types include early age of firstsexual intercourse, multiple sexual partners, smoking, andpoor immune function.[1] These types are typically spread by sustained direct skin-to-skin contact, withvaginal andanal sex being the most common methods.[4] HPV infection can alsospread from a mother to baby during pregnancy.[12] There is no evidence that HPV can spread via common items like toilet seats,[14] but the types that cause warts may spread via surfaces such as floors.[15] HPV is not killed by common hand sanitizers and disinfectants, increasing the possibility of the virus being transferred via non-living infectious agents calledfomites.[16]
HPV vaccines can prevent the most common types of infection.[4] To be most effective, inoculation should occur before the onset of sexual activity, and are therefore recommended between the ages of 9–13 years.[1] For children between the ages of 9–14 years, vaccination effectiveness is reported to range between 74% and 93%, decreasing to 12% to 90% for 15–18 year old adolescents.[17]Cervical cancer screening, such as thePapanicolaou test ("pap smear"), or examination of the cervix after applyingacetic acid, can detect both early cancer and abnormal cells that may develop into cancer.[1] Screening allows for early treatment which results in better outcomes.[1] Screening has reduced both the number of cases and the number of deaths from cervical cancer.[18] Genital warts can be removed byfreezing.[5]
Nearly every sexually active individual is infected by HPV at some point in their lives.[4] HPV is the most commonsexually transmitted infection (STI), globally.[5] High-risk HPVs cause about 5% of all cancers worldwide and about 37,300 cases of cancer in the United States each year.[11] Cervical cancer is among the most common cancers worldwide, causing an estimated 604,000 new cases and 342,000 deaths in 2020.[1] About 90% of these new cases and deaths of cervical cancer occurred inlow- and middle-income countries.[1] Roughly 1% of sexually active adults have genital warts.[12] Cases of skin warts have been described since the time ofancient Greece, but it was not until 1907 that they were determined to be caused by a virus.[19]
HPV is a group of more than 200 related viruses, which are designated by a number for each virus type.[11] Some HPV types, such as HPV5, may establish infections that persist for the lifetime of the individual without ever manifesting any clinical symptoms. HPV types 1 and 2 can cause common warts in some infected individuals.[20] HPV types 6 and 11 can cause genital warts andlaryngeal papillomatosis.[1]
Many HPV types arecarcinogenic.[21] About twelve HPV types (including types 16, 18, 31, and 45) are called "high-risk" types because persistent infection has been linked to cancer of theoropharynx,[3]larynx,[3]vulva,vagina,cervix,penis, andanus.[11][22][23] These cancers all involve sexually transmitted infection of HPV to thestratified epithelial tissue.[1][2] HPV type 16 is the strain most likely to cause cancer and is present in about 47% of all cervical cancers,[24][25] and in many vaginal and vulvar cancers,[26] penile cancers, anal cancers, and cancers of the head and neck.
The table below lists common symptoms of HPV infection and the associated types of HPV.
AvailableHPV vaccines protect against either two, four, or nine types of HPV.[30] There are six prophylactic HPV vaccines licensed for use: the bivalent vaccinesCervarix,Cecolin, andWalrinvax; the quadrivalent vaccinesCervavax andGardasil; and the nonavalent vaccineGardasil 9.[30] All HPV vaccines protect against at least HPV types 16 and 18, which cause the greatest risk of cervical cancer. The quadrivalent vaccines also protect against HPV types 6 and 11. The nonavalent vaccine Gardasil 9 provides protection against those four types (6, 11, 16, and 18), along with five other high-risk HPV types responsible for 20% of cervical cancers (types 31, 33, 45, 52, and 58).[30]
PapillomaA sample DNA test report for HPV genotype from a laboratory
Skin infection ("cutaneous" infection) with HPV is very widespread.[31]Skin infections with HPV can cause noncancerous skin growths calledwarts (verrucae). Warts are caused by the rapid growth of cells on the outer layer of the skin.[32]While cases of warts have been described since the time of ancient Greece, their viral cause was not known until 1907.[19]
Skin warts are most common in childhood and typically appear and regress spontaneously over weeks to months. Recurring skin warts are common.[33] All HPVs are believed to be capable of establishing long-term "latent" infections in small numbers ofstem cells present in the skin. Although these latent infections may never be fully eradicated, immunological control is thought to block the appearance of symptoms such as warts. Immunological control is HPV type-specific, meaning an individual may become resistant to one HPV type while remaining susceptible to other types.[citation needed]
Types of warts include:
Common warts are usually found on the hands and feet, but can also occur in other areas, such as the elbows or knees. Common warts have a characteristiccauliflower-like surface and are typically slightly raised above the surrounding skin. Cutaneous HPV types can cause genital warts but are not associated with the development of cancer.[citation needed]
Plantar warts are found on the soles of the feet; they grow inward, generally causing pain when walking.
Subungual orperiungual warts form under thefingernail (subungual), around the fingernail, or on thecuticle (periungual). They are more difficult to treat than warts in other locations.[34]
Flat warts are most commonly found on the arms, face, or forehead. Like common warts, flat warts occur most frequently in children and teens. In people with normal immune function, flat warts are not associated with the development of cancer.[35]
Common, flat, and plantar warts are much less likely to spread from person to person.
HPV infection of the skin in the genital area is the most common sexually transmitted infection worldwide.[36] Such infections are associated withgenital or anal warts (medically known as condylomata acuminata or venereal warts), and these warts are the most easily recognized sign of genital HPV infection.[citation needed]
The strains of HPV that can cause genital warts are usually different from those that cause warts on other parts of the body, such as the hands or feet, or even the inner thighs. A wide variety of HPV types can cause genital warts, but types 6 and 11 together account for about 90% of all cases.[37][38] However, in total more than 40 types of HPV are transmitted through sexual contact and can infect the skin of the anus and genitals.[4] Such infections may cause genital warts, although they may also remain asymptomatic.[citation needed]
The great majority of genital HPV infections never cause any overt symptoms and are cleared by the immune system in a matter of months. Moreover, people may transmit the virus to others even if they do not display overt symptoms of infection. Most people acquire genital HPV infections at some point in their lives, and about 10% of women are currently infected.[36] A large increase in the incidence of genital HPV infection occurs at the age when individuals begin to engage in sexual activity. As with cutaneous HPVs, immunity to genital HPV is believed to be specific to a specific strain of HPV.[citation needed]
In addition to genital warts, infection by HPV types 6 and 11 can cause a rare condition known as recurrentlaryngeal papillomatosis, in which warts form on thelarynx[39] or other areas of the respiratory tract.[40][41]These warts can recur frequently, may interfere with breathing, and in extremely rare cases can progress to cancer. For these reasons, repeated surgery to remove the warts may be advisable.[40][42]
Cervical cancer is among the most common cancers worldwide, causing an estimated 604,000 new cases and 342,000 deaths in 2020.[1] About 90% of these new cases and deaths of cervical cancer occurred inlow- and middle-income countries, where screening tests and treatment of early cervical cell changes are not readily available.[1]
In the United States, about 37,300 cases of cancer due to HPV occur each year.[11]
The number of HPV-associated cancers in the period of 2008–2012 in the U.S.[43]
Genome organization of human papillomavirus type 16, one of the subtypes known to cause cervical cancer (E1-E7 early genes, L1-L2 late genes: capsid)
In some infected individuals, their immune systems may fail to control HPV. Lingering infection with high-risk HPV types, such as types 16, 18, 31, and 45, can favor the development of cancer.[44]Co-factors such as cigarette smoke can also enhance the risk of HPV-related cancers.[45][46]
HPV is believed to cause cancer by integrating its genome intonuclear DNA. Some of the early genes expressed by HPV, such as E6 and E7, act asoncogenes that promote tumor growth andmalignant transformation.[19] HPV genome integration can also causecarcinogenesis by promoting genomic instability associated with alterations in DNA copy number.[47]
E6 produces a protein (also called E6) that simultaneously binds to two host cell proteins calledp53 and E6-Associated Protein (E6-AP). E6AP is an E3Ubiquitin ligase, an enzyme whose purpose is to tag proteins with apost-translational modification called Ubiquitin. By binding both proteins, E6 induces E6AP to attach a chain ofubiquitin molecules to p53, thereby flagging p53 forproteosomal degradation.[48][49] Normally, p53 acts to prevent cell growth and promotescell death in the presence of DNA damage. p53 also upregulates the p21 protein, which blocks the formation of thecyclin D/Cdk4 complex, thereby preventing the phosphorylation ofretinoblastoma protein (RB), and in turn, halting cell cycle progression by preventing the activation ofE2F. In short, p53 is a tumor-suppressor protein that arrests the cell cycle and prevents cell growth and survival when DNA damage occurs.[50] Thus, the degradation of p53, induced by E6, promotes unregulated cell division, cell growth and cell survival, all characteristics of cancer.[51]
It is important to note, that while the interaction between E6, E6AP, and p53 was the first to be characterized, there are multiple other proteins in the host cell which interact with E6 and assist in the induction of cancer.[52]
Artist's impression of cervical cancer caused by HPV.
Nearly all cases ofcervical cancer are associated with HPV infection, with two types, HPV16 and HPV18, present in 70% of cases.[1][7][24][54][55][56] In 2012, twelve HPV types were considered carcinogenic for cervical cancer by theInternational Agency for Research on Cancer: 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, and 59.[57] One study found that 74% of squamous cell carcinomas and 78% of adenocarcinomas tested positive for HPV types 16 or 18.[58] Persistent HPV infection increases the risk for developing cervical carcinoma. Individuals who have an increased incidence of these types of infection are women with HIV/AIDS, who are at a 22-fold increased risk of cervical cancer.[59][60]
The carcinogenic HPV types in cervical cancer belong to thealphapapillomavirus genus and can be grouped further into HPVclades.[61] The two major carcinogenic HPV clades, alphapapillomavirus-9 (A9) and alphapapillomavirus-7 (A7), containHPV16 andHPV18, respectively.[62] These two HPV clades were shown to have different effects on tumour molecular characteristics and patient prognosis, with clade A7 being associated with more aggressive pathways and an inferior prognosis.[63]
In 2020, about 604,000 new cases and 342,000 deaths from cervical cancer occurred worldwide. Around 90% of these occurred in thedeveloping world.[1]
Most HPV infections of the cervix are cleared rapidly by the immune system and do not progress to cervical cancer (see below theClearance subsection in Virology). Because the process of transforming normal cervical cells into cancerous ones is slow, cancer occurs in people having been infected with HPV for a long time, usually over a decade or more (persistent infection).[40][64] Furthermore, both the HPV infection and cervical cancer drive metabolic modifications that may be correlated with the aberrant regulation of enzymes related to metabolic pathways.[65]
Non-European (NE) HPV16 variants are significantly more carcinogenic than European (E) HPV16 variants.[66]
The risk for anal cancer is 17 to 31 times higher among HIV-positive individuals who were coinfected with high-risk HPV, and 80 times higher for particularly HIV-positive men who have sex with men.[67]
Anal Pap smear screening for anal cancer might benefit some subpopulations of men or women engaging in anal sex.[68] No consensus exists, though, that such screening is beneficial, or who should get an anal Pap smear.[69][70]
HPV is associated with approximately 50% ofpenile cancers. In the United States, penile cancer accounts for about 0.5% of all cancer cases in men. HPV16 is the most commonly associated type detected. The risk of penile cancer increases 2- to 3-fold for individuals who are infected with HIV as well as HPV.[67]
The local percentage varies widely, from 70% in the United States[76] to 4% in Brazil.[77] Engaging in anal or oral sex with an HPV-infected partner may increase the risk of developing these types of cancers.[72]
In the United States, the number of newly diagnosed, HPV-associated head and neck cancers has surpassed that of cervical cancer cases.[71] The rate of such cancers has increased from an estimated 0.8 cases per 100,000 people in 1988[78] to 4.5 per 100,000 in 2012,[43] and, as of 2021, the rate has continued to increase.[79] Researchers explain these recent data by an increase in oral sex. This type of cancer is more common in men than in women.[80]
The mutational profile of HPV-positive and HPV-negative head and neck cancer has been reported, further demonstrating that they are fundamentally distinct diseases.[81]
Some evidence links HPV to benign and malignant tumors of the upper respiratory tract. The International Agency for Research on Cancer has found that people with lung cancer were significantly more likely to have several high-risk forms of HPV antibodies compared to those who did not have lung cancer.[82] Researchers looking for HPV among 1,633 lung cancer patients and 2,729 people without the lung disease found that people with lung cancer had more types of HPV than noncancer patients did, and among lung cancer patients, the chances of having eight types of serious HPV were significantly increased.[83] In addition, expression of HPV structural proteins by immunohistochemistry andin vitro studies suggest HPV presence in bronchial cancer and its precursor lesions.[84] Another study detected HPV in theexhaled breath condensate (EBC), bronchial brushing and neoplastic lung tissue of cases, and found a presence of an HPV infection in 16.4% of the subjects affected by nonsmall cell lung cancer, but in none of the controls.[85] The reported average frequencies of HPV in lung cancers were 17% and 15% in Europe and the Americas, respectively, and the mean number of HPV in Asian lung cancer samples was 35.7%, with considerable heterogeneity between certain countries and regions.[86]
In very rare cases, HPV may causeepidermodysplasia verruciformis (EV) in individuals with aweakened immune system. The virus, unchecked by the immune system, causes the overproduction ofkeratin byskin cells, resulting in lesions resembling warts orcutaneous horns which can ultimately transform intoskin cancer, but the development is not well understood.[87][88] The specific types of HPV that are associated with EV are HPV5, HPV8, and HPV14.[88]
Sexually transmitted HPV is divided into two categories: low-risk and high-risk. Low-risk HPVs cause warts on or around the genitals. Type 6 and 11 cause 90% of all genital warts and recurrent respiratory papillomatosis that causes benign tumors in the air passages. High-risk HPVs cause cancer and consist of about twelve identified types.[11] Types 16 and 18 are responsible for causing most of HPV-caused cancers. These high-risk HPVs cause 5% of the cancers in the world. In the United States, high-risk HPVs cause 3% of all cancer cases in women and 2% in men.[89]
Risk factors for persistent genital HPV infections, which increase the risk of developing cancer, include early age of first sexual intercourse, multiple partners, smoking, and immunosuppression.[1] Genital HPV is spread by sustained direct skin-to-skin contact, with vaginal, anal, and oral sex being the most common methods.[4][22] Occasionally, it can spread frommanual sex orfrom a mother to her baby during pregnancy.[90][91] HPV is difficult to remove via standard hospital disinfection techniques and may be transmitted in a healthcare setting on re-usable gynecological equipment, such as vaginal ultrasound transducers. The period of communicability is still unknown, but probably at least as long as visible HPV lesions persist. HPV may still be transmitted even after lesions are treated and no longer visible or present.[92]
Although genital HPV types can be transmitted from mother to child during birth, the appearance of genital HPV-related diseases in newborns is rare. However, the lack of appearance does not rule out asymptomatic latent infection, as the virus has proven to be capable of hiding for decades.Perinatal transmission of HPV types 6 and 11 can result in the development of juvenile-onset recurrentrespiratory papillomatosis (JORRP). JORRP is very rare, with rates of about 2 cases per 100,000 children in the United States.[40] Although JORRP rates are substantially higher if a woman presents with genital warts at the time of giving birth, the risk of JORRP in such cases is still less than 1%.[citation needed]
Genital HPV infections are transmitted primarily by contact with the genitals, anus, or mouth of an infected sexual partner.[93]
Of the 120 known human papillomaviruses, 51 species and three subtypes infect the genital mucosa.[94] Fifteen are classified as high-risk types (16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 68, 73, and 82), three as probable high-risk (26, 53, and 66), and twelve as low-risk (6, 11, 40, 42, 43, 44, 54, 61, 70, 72, 81, and 89).[21]
Condoms do not completely protect from the virus because the areas around the genitals including the inner thigh area are not covered, thus exposing these areas to the infected person's skin.[95]
Studies have shown HPV transmission between the hands and genitals of the same person and sexual partners. Hernandez tested the genitals and dominant hand of each person in 25 heterosexual couples every other month for an average of seven months. She found two couples where the man's genitals infected the woman's hand with high-risk HPV, two where her hand infected his genitals, one where her genitals infected his hand, two each where he infected his own hand, and she infected her own hand.[96] Hands were not the main source of transmission in these 25 couples, but they were significant.[citation needed]
Partridge reports men's fingertips became positive for high-risk HPV at more than half the rate (26% per two years) as their genitals (48%).[97] Winer reports 14% of fingertip samples from sexually active women were positive.[98]
Non-sexual hand contact seems to have little or no role in HPV transmission. Winer found all fourteen fingertip samples from virgin women negative at the start of her fingertip study.[98] In a separate report on genital HPV infection, 1% of virgin women (1 of 76) with no sexual contact tested positive for HPV, while 10% of virgin women reporting non-penetrative sexual contact were positive (7 of 72).[99]
Sharing of possibly contaminated objects, for example, razors,[92] may transmit HPV.[100][101][102] Although possible, transmission by routes other than sexual intercourse is less common for female genital HPV infection.[93] Fingers-genital contact is a possible way of transmission but unlikely to be a significant source.[98][103]
Though it has traditionally been assumed that HPV is not transmissible via blood – as it is thought to only infect cutaneous and mucosal tissues – recent studies have called this notion into question. Historically, HPV DNA has been detected in the blood of cervical cancer patients.[104] In 2005, a group reported that, in frozen blood samples of 57 sexually naive pediatric patients who hadvertical ortransfusion-acquired HIV infection, 8 (14.0%) of these samples also tested positive for HPV-16.[105] This seems to indicate that it may be possible for HPV to be transmitted viablood transfusion. However, as non-sexual transmission of HPV by other means is not uncommon, this could not be definitively proven. In 2009, a group testedAustralian Red Cross blood samples from 180 healthy male donors for HPV, and subsequently found DNA of one or more strains of the virus in 15 (8.3%) of the samples.[106] However, it is important to note that detecting the presence of HPV DNA in blood is not the same as detecting the virus itself in blood, and whether or not the virus itself can or does reside in blood in infected individuals is still unknown. As such, it remains to be determined whether HPV can or cannot be transmitted via blood.[104] This is of concern, as blood donations are not currently screened for HPV, and at least some organizations such as theAmerican Red Cross and other Red Cross societies do not presently appear to disallow HPV-positive individuals from donating blood.[107]
Hospital transmission of HPV, especially to surgical staff, has been documented. Surgeons, including urologists and/or anyone in the room, are subject to HPV infection by inhalation of noxious viral particles duringelectrocautery orlaser ablation of a condyloma (wart).[108] There has been a case report of a laser surgeon who developed extensive laryngeal papillomatosis after providing laser ablation to patients with anogenital condylomata.[108]
HPV infection is limited to thebasal cells ofstratified epithelium, the only tissue in which they replicate.[110] The virus cannot bind to live tissue; instead, it infectsepithelial tissues through micro-abrasions or other epithelial trauma that exposes segments of thebasement membrane.[110] The infectious process is slow, taking 12–24 hours for initiation of transcription. It is believed that involved antibodies play a major neutralizing role while thevirions still reside on the basement membrane and cell surfaces.[110]
HPV lesions are thought to arise from the proliferation of infected basalkeratinocytes. Infection typically occurs when basal cells in the host are exposed to the infectious virus through a disturbed epithelial barrier as would occur during sexual intercourse or after minor skin abrasions. HPV infections have not been shown to becytolytic; rather, viral particles are released as a result of degeneration ofdesquamating cells. HPV can survive for many months and at low temperatures without a host; therefore, an individual with plantar warts can spread the virus by walking barefoot.[38]
HPV is a small double-stranded circular DNA virus with a genome of approximately 8000 base pairs.[22][111] The HPV life cycle strictly follows the differentiation program of the host keratinocyte. It is thought that the HPVvirion infectsepithelial tissues through micro-abrasions, whereby the virion associates with putative receptors such as alphaintegrins,laminins, andannexin A2[112] leading to the entry of the virions intobasal epithelial cells throughclathrin-mediated endocytosis and/orcaveolin-mediated endocytosis depending on the type of HPV.[113] At this point, the viralgenome is transported to the nucleus by unknown mechanisms and establishes itself at a copy number of 10-200 viral genomes per cell. A sophisticatedtranscriptional cascade then occurs as the host keratinocyte begins to divide and become increasingly differentiated in the upper layers of the epithelium.[citation needed]
The phylogeny of the various strains of HPV generally reflects the migration patterns ofHomo sapiens and suggests that HPV may have diversified along with the human population. Studies suggest that HPV evolved along five major branches that reflect the ethnicity of human hosts, and diversified along with the human population.[114]
Researchers initially identified two major variants of HPV16, European (HPV16-E), and Non-European (HPV16-NE).[115] More recent analyses based on thousands of HPV16 genomes show that indeed two major clades exist, that are further subdivided into four lineages (designated A-D) and even further subdivided into 16 sublineages (A1–4, B1–4, C1–4 and D1–4).[116][117] The A1-A3 sublineages constitute the European variant, A4 the Asian variant, B1-B4 the African type I variant, C1–C4 the African type II variant, D1 the North American variant, D2 the Asian American type I variant, D3 the Asian American type II variant.[116] The various lineages and sublineages have different oncogenic capacity, where overall, the non-European lineages are considered to increase the risk for cancer.[118] Although HPV16 is a DNA virus, there are signs of recombination among the different lineages.[117][119] Based on an analysis of more than 3600 genomes, between 0.3 and 1.2% of them could be recombinant.[117] Thus, ideally, genotyping (for cancer-risk assessment) of HPV16 should not be based only on certain genes, but on all genes from the entire genome.[117]
A bioinformatics tool named HPV16-Genotyper performs i) HPV16 lineage genotyping, ii) detects potential recombination events, iii) identifies, within the submitted sequences, mutations/SNPs that have been reported (in literature) to increase the risk for cancer.[117]
Structure of the HPV type 16 oncoprotein E6 (purple), as obtained byX-ray crystallography, shown bound to the LxxLLpeptide motif of the human proteinUBE3A (cyan). Rendered fromPDB:4GIZ.[120]
The two primary oncoproteins of high-risk HPV types are E6 and E7. The "E" designation indicates that these two proteins areearly proteins (expressed early in the HPV life cycle), while the "L" designation indicates that they arelate proteins (late expression).[55] The HPV genome is composed of six early (E1, E2, E4, E5, E6, and E7)open reading frames (ORF), two late (L1 and L2) ORFs, and a non-coding long control region (LCR).[121] After the host cell is infected viral early promoter is activated and a polycistronic primary RNA containing all six early ORFs is transcribed. This polycistronic RNA then undergoes active RNA splicing to generate multiple isoforms ofmRNAs.[122] One of the spliced isoform RNAs, E6*I, serves as an E7 mRNA to translate E7 protein.[123] However, viral early transcription subjects to viral E2 regulation and high E2 levels repress the transcription. HPV genomes integrate into the host genome by disruption of E2 ORF, preventing E2 repression on E6 and E7. Thus, viral genome integration into the host DNA genome increases E6 and E7 expression to promote cellular proliferation and the chance of malignancy. The degree to which E6 and E7 are expressed is correlated with the type of cervical lesion that can ultimately develop.[111]
Role in cancer
Sometimes papillomavirus genomes are found integrated into the host genome, and this is especially noticeable with oncogenic HPVs.[124] The E6/E7 proteins inactivate two tumor suppressor proteins,p53 (inactivated by E6) andpRb (inactivated by E7).[125] The viraloncogenes E6 and E7[126] are thought to modify the cell cycle so as to retain the differentiating host keratinocyte in a state that is favourable to the amplification of viral genome replication and consequent late gene expression. E6 in association with host E6-associated protein, which has ubiquitin ligase activity, acts to ubiquitinate p53, leading to its proteosomal degradation. E7 (in oncogenic HPVs) acts as the primary transforming protein. E7 competes forretinoblastoma protein (pRb) binding, freeing the transcription factorE2F to transactivate its targets, thus pushing the cell cycle forward. All HPV can induce transient proliferation, but only strains 16 and 18 can immortalize cell linesin vitro. It has also been shown that HPV 16 and 18 cannot immortalize primaryrat cells alone; there needs to be activation of theras oncogene. In the upper layers of the host epithelium, the late genes L1 and L2 are transcribed/translated and serve as structural proteins that encapsidate the amplified viral genomes. Once the genome is encapsidated, the capsid appears to undergo a redox-dependent assembly/maturation event, which is tied to a natural redox gradient that spans both suprabasal and cornified epithelial tissue layers. This assembly/maturation event stabilizes virions and increases their specific infectivity.[127] Virions can then be sloughed off in the deadsquames of the host epithelium and the viral lifecycle continues.[128] A 2010 study has found that E6 and E7 are involved inbeta-catenin nuclear accumulation and activation ofWnt signaling in HPV-induced cancers.[129]
Once an HPV virion invades a cell, an active infection occurs, and the virus can be transmitted. Several months to years may elapse before squamous intraepithelial lesions (SIL) develop and can be clinically detected. The time from active infection to clinically detectable disease may make it difficult for epidemiologists to establish which partner was the source of infection.[108]
Most HPV infections are cleared up by most people without medical action or consequences. The table provides data for high-risk types (i.e. the types found in cancers).[citation needed]
Clearing an infection does not always create immunity if there is a new or continuing source of infection. Hernandez' 2005-6 study of 25 couples reports "A number of instances indicated apparent reinfection [from partner] after viral clearance."[96]
Over 200 types of HPV have been identified, and they are designated by numbers.[11][8][125] They may be divided into "low-risk" and "high-risk" types. Low-risk types cause warts and high-risk types can cause lesions or cancer.[132][133]
Guidelines from theAmerican Cancer Society recommend different screening strategies for cervical cancer based on a woman's age, screening history, risk factors, and choice of tests.[134] Because of the link between HPV and cervical cancer, the ACS currently recommends early detection of cervical cancer in average-risk asymptomatic adults primarily with cervical cytology by Pap smear, regardless of HPV vaccination status. Women aged 30–65 should preferably be tested every 5 years with both the HPV test and the Pap test. In other age groups, a Pap test alone can suffice unless they have been diagnosed withatypical squamous cells of undetermined significance (ASC-US).[135] Co-testing with a Pap test and HPV test is recommended because it decreases the rate of false-negatives. According to the National Cancer Institute, "The most common test detects DNA from several high-risk HPV types, but it cannot identify the types that are present. Another test is specific for DNA from HPV types 16 and 18, the two types that cause most HPV-associated cancers. A third test can detect DNA from several high-risk HPV types and can indicate whether HPV-16 or HPV-18 is present. A fourth test detects RNA from the most common high-risk HPV types. These tests can detect HPV infections before cell abnormalities are evident.[citation needed]
"Theoretically, the HPV DNA and RNA tests could be used to identify HPV infections in cells taken from any part of the body. However, the tests are approved by the FDA for only two indications: for follow-up testing of women who seem to have abnormal Pap test results and for cervical cancer screening in combination with aPap test among women over age 30."[136]
Guidelines for oropharyngeal cancer screening by the Preventive Services Task Force andAmerican Dental Association in the U.S. suggest conventional visual examination, but because some parts of the oropharynx are hard to see, this cancer is often only detected in later stages.[67]
The diagnosis of oropharyngeal cancer occurs by biopsy of exfoliated cells or tissues. TheNational Comprehensive Cancer Network andCollege of American Pathologists recommend testing for HPV in oropharyngeal cancer.[67] However, while testing is recommended, there is no specific type of test used to detect HPV from oral tumors that is currently recommended by the FDA in the United States. Because HPV type 16 is the most common type found in oropharyngeal cancer, p16immunohistochemistry is one test option used to determine if HPV is present,[137] which can help determine course of treatment since tumors that are negative for p16 have better outcomes. Another option that has emerged as a reliable option is HPV DNAin situ hybridization (ISH) which allows for visualization of the HPV.[67]
There is not a wide range of tests available even though HPV is common; most studies of HPV used tools and custom analysis not available to the general public.[138][needs update] Clinicians often depend on the vaccine among young people and high clearance rates (seeClearance subsection in Virology) to create a low risk of disease and mortality, and treat the cancers when they appear. Others believe that reducing HPV infection in more men and women, even when it has no symptoms, is important (herd immunity) to prevent more cancers rather than just treating them.[139][140][needs update] Where tests are used, negative test results show safety from transmission, and positive test results show where shielding (condoms, gloves) is needed to prevent transmission until the infection clears.[141]
Studies have tested for and found HPV in men, including high-risk types (i.e. the types found in cancers), on fingers, mouth, saliva, anus, urethra, urine, semen, blood, scrotum and penis.[138]
The aforementioned Qiagen/Digene kit was successfully usedoff-label to test the penis, scrotum, and anus[142] of men in long-term relationships with women who were positive for high-risk HPV. Of these men, 60% were found to carry the virus, primarily on the penis.[142][needs update] Similar studies have been conducted on women using cytobrushes - an endocervical brush for sampling the cervix in females - and custom analysis.[143][144][needs update]
In one study researchers sampled subjects' urethra, scrotum, and penis.[143][144][needs update] Samples taken from the urethra added less than 1% to the HPV rate. Studies like this led Giuliano to recommend sampling the glans, shaft, and crease between them, along with the scrotum, since sampling the urethra or anus added very little to the diagnosis.[97] Dunne recommends the glans, shaft, their crease, and the foreskin.[138]
In one study the subjects were asked not to wash their genitals for 12 hours before sampling, including the urethra as well as the scrotum and the penis.[143] Other studies are silent on washing – a particular gap in studies of the hands.[citation needed]
One small study used wet cytobrushes, rather than wet the skin.[144] It found a higher proportion of men to be HPV-positive when the skin was rubbed with a 600 grit emery paper before being swabbed with the brush, rather than swabbed with no preparation. It's unclear whether the emery paper collected the virions or simply loosened them for the swab to collect.[citation needed]
Studies have found self-collection (with emery paper and Dacron swabs) as effective as collection done by a clinician, and sometimes more so, since patients were more willing than a clinician to scrape vigorously.[145][needs update][146] Women had similar success in self-sampling using tampons, swabs, cytobrushes, and lavage.[147][needs update]
Several studies used cytobrushes to sample fingertips and under fingernails, without wetting the area or the brush.[98][103][148][needs update]
Other studies analyzed urine, semen, and blood and found varying amounts of HPV,[138] but there is not a publicly available test for those yet.
Although it is possible to test for HPV DNA in other kinds of infections,[138] there are no FDA-approved tests for general screening in the United States[149] or tests approved by the Canadian government,[150] since the testing is inconclusive and considered medically unnecessary.[151]
Genital warts are the only visible sign of low-risk genital HPV and can be identified with a visual check. These visible growths, however, are the result of non-carcinogenic HPV types. Five percent acetic acid (vinegar) is used to identify both warts and squamous intraepithelial neoplasia (SIL) lesions with limited success[citation needed] by causing abnormal tissue to appear white, but most doctors have found this technique helpful only in moist areas, such as the female genital tract.[citation needed] At this time, HPV tests for males are used only in research.[citation needed]
Research into testing for HPV by antibody presence has been done. The approach is looking for an immune response in blood, which would contain antibodies for HPV if the patient is HPV positive.[152][153][154][155] The reliability of such tests has not been proven, as there has not been a FDA approved product as of August 2018;[156] testing by blood would be a less invasive test for screening purposes.
TheHPV vaccines can prevent the most common types of infection.[4] To be effective they must be used before an infection occurs and are therefore recommended between the ages of nine and thirteen.Cervical cancer screening, such as with thePapanicolaou test (pap) or looking at the cervix after usingacetic acid, can detect early cancer or abnormal cells that may develop into cancer. This allows for early treatment which results in better outcomes.[1] Screening has reduced both the number and deaths from cervical cancer in the developed world.[18] Warts can be removed byfreezing.[5]
Three vaccines are available to prevent infection by some HPV types:Gardasil,Gardasil 9 andCervarix; all three protect against initial infection with HPV types 16 and 18, which cause most of the HPV-associated cancer cases. Gardasil also protects against HPV types 6 and 11, which cause 90% of genital warts. Gardasil is a recombinant quadrivalent vaccine, whereas Cervarix is bivalent, and is prepared from virus-like particles (VLP) of the L1capsid protein. Gardasil 9 is nonavalent, having the potential to prevent about 90% of cervical, vulvar, vaginal, and anal cancers. It can protect for HPV types 6, 11, 16, 18, 31, 33, 45, 52, and 58; the latter five cause up to 20% of cervical cancers which were not previously covered.[157]
The vaccines provide little benefit to women already infected with HPV types 16 and 18.[158] For this reason, the vaccine is recommended primarily for those women not yet having been exposed to HPV during sex. TheWorld Health Organization position paper on HPV vaccination clearly outlines appropriate, cost-effective strategies for using HPV vaccine in public sector programs.[159]
There is high-certainty evidence that HPV vaccines protect against precancerous cervical lesions in young women, particularly those vaccinated aged 15 to 26.[160] HPV vaccines do not increase the risk of serious adverse events.[160] Longer follow-up is needed to monitor the impact of HPV vaccines on cervical cancer.[160]
The CDC recommends the vaccines be delivered in two shots at an interval of at least 6 months for those aged 11–12, and three doses for those 13 and older.[161] In most countries, they are funded only for female use, but are approved for male use in many countries, and funded for teenage boys in Australia. The vaccine does not have any therapeutic effect on existing HPV infections or cervical lesions.[162] In 2010, 49% of teenage girls in the US got the HPV vaccine.[citation needed]
Following studies suggesting that the vaccine is more effective in younger girls[163] than in older teenagers, the United Kingdom, Switzerland, Mexico, the Netherlands, and Quebec began offering the vaccine in a two-dose schedule for girls aged under 15 in 2014.[citation needed]
Cervical cancer screening recommendations have not changed for females who receive the HPV vaccine. It remains a recommendation that women continue cervical screening, such as Pap smear testing, even after receiving the vaccine, since it does not prevent all types of cervical cancer.[162][164]
Both men and women are carriers of HPV.[165] The Gardasil vaccine also protects men against anal cancers and warts and genital warts.[166]
Duration of both vaccines' efficacy has been observed since they were first developed, and is expected to be long-lasting.[167]
In December 2014, theFDA approved a nine-valent Gardasil-based vaccine, Gardasil 9, to protect against infection with the four strains of HPV covered by the first generation of Gardasil as well as five other strains responsible for 20% of cervical cancers (HPV-31, HPV-33, HPV-45, HPV-52, and HPV-58).[168]
TheCenters for Disease Control and Prevention says that male "condom use may reduce the risk for genital human papillomavirus (HPV) infection" but provides a lesser degree of protection compared with other sexual transmitted infections "because HPV also may be transmitted by exposure to areas (e.g., infected skin or mucosal surfaces) that are not covered or protected by the condom."[169]
The virus is unusually hardy and is immune to most common disinfectants. It is the first virus ever shown to be resistant to inactivation byglutaraldehyde, which is among the most common strong disinfectants used in hospitals.[170] Dilutedsodium hypochlorite bleach is effective,[170] but cannot be used on some types of re-usable equipment, such as ultrasound transducers.[90] As a result of these difficulties, there is developing concern about the possibility of transmitting the virus on healthcare equipment, particularly reusable gynecological equipment that cannot beautoclaved.[171][172] For such equipment, some health authorities encourage use ofUV disinfection[173] or a non-hypochlorite "oxidizing‐based high‐level disinfectant [bleach] with label claims for non‐enveloped viruses",[174] such as a stronghydrogen peroxide solution[175][173] orchlorine dioxide wipes.[173] Such disinfection methods are expected to be relatively effective against HPV.[citation needed]
There is currently no specific treatment for HPV infection.[176][177][178] However, the viral infection is usually cleared to undetectable levels by the immune system.[179] According to theCenters for Disease Control and Prevention, the body's immune system clears HPV naturally within two years for 90% of cases (seeClearance subsection in Virology for more detail).[176] However, experts do not agree on whether the virus is eliminated or reduced to undetectable levels, and it is difficult to know when it is contagious.[180][needs update]
Follow up care is usually recommended and practiced by many health clinics.[181] Follow-up is sometimes not successful because a portion of those treated do not return to be evaluated. In addition to the normal methods of phone calls and mail, text messaging and email can improve the number of people who return for care.[182] As of 2015 it is unclear the best method of follow up following treatment ofcervical intraepithelial neoplasia.[183]
Globally, 12% of women are positive for HPV DNA, with rates varying by age and country.[184] The highest rates of HPV are in younger women, with a rate of 24% in women under 25 years.[185] Rates decline in older age groups in Europe and the Americas, but less so in Africa and Asia. The rates are highest in Sub-Saharan Africa (24%) and Eastern Europe (21%) and lowest in North America (5%) and Western Asia (2%).[184]
The most common types of HPV worldwide are HPV16 (3.2%), HPV18 (1.4%), HPV52 (0.9%), HPV31 (0.8%), and HPV58 (0.7%). High-risk types of HPV are also distributed unevenly, with HPV16 having a rate of around 13% in Africa and 30% in West and Central Asia.[185]
Like many diseases, HPV disproportionately affects low-income and resource-poor countries. The higher rates of HPV in Sub-Saharan Africa, for example, may be related to high exposure tohuman immunodeficiency virus (HIV) in the region. Other factors that impact the global spread of disease are sexual behaviors including age of sexual debut, number of sexual partners, and ease of access to barrier contraception, all of which vary globally.[184][186]
HPV prevalence among women by age, including 20 low-risk types and 23 high-risk types[187]
Age (years)
Prevalence (%)
14 to 19
24.5%
20 to 24
44.8%
25 to 29
27.4%
30 to 39
27.5%
40 to 49
25.2%
50 to 59
19.6%
14 to 59
26.8%
HPV is estimated to be the most common sexually transmitted infection in the United States.[187] Most sexually active men and women will probably acquire genital HPV infection at some point in their lives.[24] TheAmerican Social Health Association estimates that about 75–80% of sexually active Americans will be infected with HPV at some point in their lifetime.[188][189] By the age of 50 more than 80% of American women will have contracted at least one strain of genital HPV.[187][190] It was estimated that, in the year 2000, there were approximately 6.2 million new HPV infections among Americans aged 15–44; of these, an estimated 74% occurred to people between ages of 15 and 24.[191] Of the STIs studied, genital HPV was the most commonly acquired.[191] In the United States, it is estimated that 10% of the population has an active HPV infection, 4% has an infection that has caused cytological abnormalities, and an additional 1% has an infection causing genital warts.[192]
Estimates of HPV prevalence vary from 14% to more than 90%.[193] One reason for the difference is that some studies report women who currently have a detectable infection, while other studies report women who have ever had a detectable infection.[194][195] Another cause of discrepancy is the difference in strains that were tested for.[citation needed]
One study found that, during 2003–2004,at any given time, 26.8% of women aged 14 to 59 were infected with at least one type of HPV. This was higher than previous estimates; 15.2% were infected with one or more of the high-risk types that can cause cancer.[187][196]
The prevalence for high-risk and low-risk types is roughly similar over time.[187]
Human papillomavirus is not included among the diseases that are typically reportable to theCDC as of 2011.[197][198]
On average 538 cases of HPV-associated cancers were diagnosed per year in Ireland during the period 2010 to 2014.[199] Cervical cancer was the most frequent HPV-associated cancer with on average 292 cases per year (74% of the female total, and 54% of the overall total of HPV-associated cancers).[199] A study of 996 cervical cytology samples in an Irish urban female, opportunistically screened population, found an overall HPV prevalence of 19.8%, HPV 16 at 20% and HPV 18 at 12% were the commonest high-risk types detected. In Europe, types 16 and 18 are responsible for over 70% of cervical cancers.[200] Overall rates of HPV-associated invasive cancers may be increasing. Between 1994 and 2014, there was a 2% increase in the rate of HPV-associated invasive cancers per year for both sexes in Ireland.[199]
As HPV is known to be associated with anogenital warts, these are notifiable to the Health Protection Surveillance Centre (HPSC). Genital warts are the second most common STI in Ireland.[201] There were 1,281 cases of anogenital warts notified in 2017, which was a decrease on the 2016 figure of 1,593.[202] The highest age-specific rate for both male and female was in the 25–29 year old age range; 53% of cases were among males.[202]
In the Autonomous Region ofInner Mongolia overall HPV prevalence is 14.5% but shows substantial ethnical disparity, the prevalence in Mongolian women (14.9%) being much higher than that of Han participants (4.3%).[204] Urbanization, the number of sex partners, and PAP history appear as risk factors for HPV infection in Han, but not in Mongolian women. The region is thus an important example that the epidemiology of HPV is more related to cultural and ethnical factors and not to geography per se.[citation needed]
One of the first studies linking risk ofuterine carcinoma with the number of sexual activity was performed in 1842, in Verona. Dr. Domenico Rigoni-Stern observed that uterine cancer incidence among Catholic nuns living in convents in the countryside was lower than in women living in the city. Highest incidence was seen for prostitutes, thereby linking uterine cancer prevalence to the number of sexual partners, and suggesting that this disease might have a sexually transmissible component.[205]
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