Association Between HLA-DRB1 polymorphism, high-risk HPV infection and cervical neoplasia in southern Chinese
Multiple determinants are involved in the progression of human papillomavirus (HPV)‐infected cervical lesion to invasive cancer. Human leukocyte antigen (HLA) polymorphism seems to play a role. This study examined the association between HLA‐DRB1 polymorphism, high‐risk HPV infection, and the develo...
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creator | Chan, Paul K.S. Cheung, Tak-Hong Lin, C. K. Siu, Shing-Shun N. Yim, So-Fan Lo, Keith W.K. Cheung, Jo L. K. Tam, Ann O.Y. Tang, Julian W. |
description | Multiple determinants are involved in the progression of human papillomavirus (HPV)‐infected cervical lesion to invasive cancer. Human leukocyte antigen (HLA) polymorphism seems to play a role. This study examined the association between HLA‐DRB1 polymorphism, high‐risk HPV infection, and the development of cervical neoplasia in southern Chinese. Three hundred and seventy women with cervical neoplasia (43 cervical intraepithelial neoplasia grade II, 154 grade III, and 173 invasive cancers) and 323 controls were recruited for HLA‐DRB1 typing by a sequence‐based approach. Cervical specimens were collected for HPV detection by a consensus primer‐based polymerase chain reaction, and with the type of HPV identified by hybridization with type‐specific oligonucleotide probes. A protective effect of HLA‐DRB1*12 for cervical neoplasia was observed, and with stronger associations when subgroup analyses were carried out for patients infected with HPV16 and HPV58. The protective effect of HLA‐DRB1*13 that had been reported from other populations was not observed. The data obtained in this study showed that HLA‐DRB1*03 conferred a higher risk for HPV18‐infected, but not for HPV16‐, HPV52‐, or HPV58‐infected cervical lesions. Although, HPV52 was reported as uncommon worldwide, it was found to be the second most prevalent type in the southern Chinese population. However, no additional risk association was observed when subgroup analyses were performed for HPV52‐infected patients. The current study shows that, among southern Chinese, the outcome of HPV‐infected cervical lesions is associated with HLA‐DRB1 polymorphism. These associations often vary with the type of HPV infection. J. Med. Virol. 79:970‐976, 2007. © 2007 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/jmv.20805 |
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K. ; Siu, Shing-Shun N. ; Yim, So-Fan ; Lo, Keith W.K. ; Cheung, Jo L. K. ; Tam, Ann O.Y. ; Tang, Julian W.</creator><creatorcontrib>Chan, Paul K.S. ; Cheung, Tak-Hong ; Lin, C. K. ; Siu, Shing-Shun N. ; Yim, So-Fan ; Lo, Keith W.K. ; Cheung, Jo L. K. ; Tam, Ann O.Y. ; Tang, Julian W.</creatorcontrib><description>Multiple determinants are involved in the progression of human papillomavirus (HPV)‐infected cervical lesion to invasive cancer. Human leukocyte antigen (HLA) polymorphism seems to play a role. This study examined the association between HLA‐DRB1 polymorphism, high‐risk HPV infection, and the development of cervical neoplasia in southern Chinese. Three hundred and seventy women with cervical neoplasia (43 cervical intraepithelial neoplasia grade II, 154 grade III, and 173 invasive cancers) and 323 controls were recruited for HLA‐DRB1 typing by a sequence‐based approach. Cervical specimens were collected for HPV detection by a consensus primer‐based polymerase chain reaction, and with the type of HPV identified by hybridization with type‐specific oligonucleotide probes. A protective effect of HLA‐DRB1*12 for cervical neoplasia was observed, and with stronger associations when subgroup analyses were carried out for patients infected with HPV16 and HPV58. The protective effect of HLA‐DRB1*13 that had been reported from other populations was not observed. The data obtained in this study showed that HLA‐DRB1*03 conferred a higher risk for HPV18‐infected, but not for HPV16‐, HPV52‐, or HPV58‐infected cervical lesions. Although, HPV52 was reported as uncommon worldwide, it was found to be the second most prevalent type in the southern Chinese population. However, no additional risk association was observed when subgroup analyses were performed for HPV52‐infected patients. The current study shows that, among southern Chinese, the outcome of HPV‐infected cervical lesions is associated with HLA‐DRB1 polymorphism. These associations often vary with the type of HPV infection. J. Med. Virol. 79:970‐976, 2007. © 2007 Wiley‐Liss, Inc.</description><identifier>ISSN: 0146-6615</identifier><identifier>EISSN: 1096-9071</identifier><identifier>DOI: 10.1002/jmv.20805</identifier><identifier>PMID: 17516530</identifier><identifier>CODEN: JMVIDB</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Asian Continental Ancestry Group - genetics ; Biological and medical sciences ; Carcinogenesis, carcinogens and anticarcinogens ; Case-Control Studies ; cervical cancer ; Cervical Intraepithelial Neoplasia - genetics ; Cervical Intraepithelial Neoplasia - immunology ; Cervical Intraepithelial Neoplasia - virology ; Chinese ; Female ; HLA ; HLA-DR Antigens - genetics ; HLA-DRB1 Chains ; Hong Kong ; host genetics ; HPV ; Human papillomavirus ; Human papillomavirus 16 ; Human papillomavirus 16 - genetics ; Human papillomavirus 16 - isolation & purification ; Human papillomavirus 16 - pathogenicity ; Humans ; Male ; Medical sciences ; Middle Aged ; Papillomaviridae - classification ; Papillomaviridae - genetics ; Papillomaviridae - isolation & purification ; Papillomaviridae - pathogenicity ; Papillomavirus Infections - genetics ; Papillomavirus Infections - immunology ; Papillomavirus Infections - virology ; Polymorphism, Genetic ; Risk Factors ; Tumors ; Uterine Cervical Neoplasms - genetics ; Uterine Cervical Neoplasms - immunology ; Uterine Cervical Neoplasms - virology ; Viruses</subject><ispartof>Journal of medical virology, 2007-07, Vol.79 (7), p.970-976</ispartof><rights>Copyright © 2007 Wiley‐Liss, Inc.</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5235-b9b1a88941c112cac89feefe8f085ff9b58a37ced49e29fd521c8bd237c4a3343</citedby><cites>FETCH-LOGICAL-c5235-b9b1a88941c112cac89feefe8f085ff9b58a37ced49e29fd521c8bd237c4a3343</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjmv.20805$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjmv.20805$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18847701$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17516530$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chan, Paul K.S.</creatorcontrib><creatorcontrib>Cheung, Tak-Hong</creatorcontrib><creatorcontrib>Lin, C. K.</creatorcontrib><creatorcontrib>Siu, Shing-Shun N.</creatorcontrib><creatorcontrib>Yim, So-Fan</creatorcontrib><creatorcontrib>Lo, Keith W.K.</creatorcontrib><creatorcontrib>Cheung, Jo L. K.</creatorcontrib><creatorcontrib>Tam, Ann O.Y.</creatorcontrib><creatorcontrib>Tang, Julian W.</creatorcontrib><title>Association Between HLA-DRB1 polymorphism, high-risk HPV infection and cervical neoplasia in southern Chinese</title><title>Journal of medical virology</title><addtitle>J. Med. Virol</addtitle><description>Multiple determinants are involved in the progression of human papillomavirus (HPV)‐infected cervical lesion to invasive cancer. Human leukocyte antigen (HLA) polymorphism seems to play a role. This study examined the association between HLA‐DRB1 polymorphism, high‐risk HPV infection, and the development of cervical neoplasia in southern Chinese. Three hundred and seventy women with cervical neoplasia (43 cervical intraepithelial neoplasia grade II, 154 grade III, and 173 invasive cancers) and 323 controls were recruited for HLA‐DRB1 typing by a sequence‐based approach. Cervical specimens were collected for HPV detection by a consensus primer‐based polymerase chain reaction, and with the type of HPV identified by hybridization with type‐specific oligonucleotide probes. A protective effect of HLA‐DRB1*12 for cervical neoplasia was observed, and with stronger associations when subgroup analyses were carried out for patients infected with HPV16 and HPV58. The protective effect of HLA‐DRB1*13 that had been reported from other populations was not observed. The data obtained in this study showed that HLA‐DRB1*03 conferred a higher risk for HPV18‐infected, but not for HPV16‐, HPV52‐, or HPV58‐infected cervical lesions. Although, HPV52 was reported as uncommon worldwide, it was found to be the second most prevalent type in the southern Chinese population. However, no additional risk association was observed when subgroup analyses were performed for HPV52‐infected patients. The current study shows that, among southern Chinese, the outcome of HPV‐infected cervical lesions is associated with HLA‐DRB1 polymorphism. These associations often vary with the type of HPV infection. J. Med. Virol. 79:970‐976, 2007. © 2007 Wiley‐Liss, Inc.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Asian Continental Ancestry Group - genetics</subject><subject>Biological and medical sciences</subject><subject>Carcinogenesis, carcinogens and anticarcinogens</subject><subject>Case-Control Studies</subject><subject>cervical cancer</subject><subject>Cervical Intraepithelial Neoplasia - genetics</subject><subject>Cervical Intraepithelial Neoplasia - immunology</subject><subject>Cervical Intraepithelial Neoplasia - virology</subject><subject>Chinese</subject><subject>Female</subject><subject>HLA</subject><subject>HLA-DR Antigens - genetics</subject><subject>HLA-DRB1 Chains</subject><subject>Hong Kong</subject><subject>host genetics</subject><subject>HPV</subject><subject>Human papillomavirus</subject><subject>Human papillomavirus 16</subject><subject>Human papillomavirus 16 - genetics</subject><subject>Human papillomavirus 16 - isolation & purification</subject><subject>Human papillomavirus 16 - pathogenicity</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Papillomaviridae - classification</subject><subject>Papillomaviridae - genetics</subject><subject>Papillomaviridae - isolation & purification</subject><subject>Papillomaviridae - pathogenicity</subject><subject>Papillomavirus Infections - genetics</subject><subject>Papillomavirus Infections - immunology</subject><subject>Papillomavirus Infections - virology</subject><subject>Polymorphism, Genetic</subject><subject>Risk Factors</subject><subject>Tumors</subject><subject>Uterine Cervical Neoplasms - genetics</subject><subject>Uterine Cervical Neoplasms - immunology</subject><subject>Uterine Cervical Neoplasms - virology</subject><subject>Viruses</subject><issn>0146-6615</issn><issn>1096-9071</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0U1vEzEQBmALgWgoHPgDyBeQkNjWH-td-5gGSEChVKgUbpbXO2bd7hf2piX_HrcJ9IQ4WJasZ2asdxB6TskRJYQdX3bXR4xIIh6gGSWqyBQp6UM0IzQvsqKg4gA9ifGSECIVY4_RAS0FLQQnM9TNYxysN5MfenwC0w1Aj1frefb2ywnF49BuuyGMjY_dG9z4H00WfLzCq7ML7HsH9q7M9DW2EK69NS3uYRhbE71JAMdhMzUQerxofA8RnqJHzrQRnu3vQ_T1_bvzxSpbf15-WMzXmRWMi6xSFTVSqpxaSpk1VioH4EA6IoVzqhLS8NJCnStgytWCUSurmqW33HCe80P0atd3DMPPDcRJdz5aaFuTvreJuiQiT0f-FzKSUsr5LXy9gzYMMQZwegy-M2GrKdG3S9BpCfpuCcm-2DfdVB3U93KfegIv98DElJkLprc-3jsp87IkNLnjnbvxLWz_PVF__HTxZ3S2q_Bxgl9_K0y40kXJS6G_nS41O-dseUa_61P-G4qArTE</recordid><startdate>200707</startdate><enddate>200707</enddate><creator>Chan, Paul K.S.</creator><creator>Cheung, Tak-Hong</creator><creator>Lin, C. K.</creator><creator>Siu, Shing-Shun N.</creator><creator>Yim, So-Fan</creator><creator>Lo, Keith W.K.</creator><creator>Cheung, Jo L. K.</creator><creator>Tam, Ann O.Y.</creator><creator>Tang, Julian W.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>200707</creationdate><title>Association Between HLA-DRB1 polymorphism, high-risk HPV infection and cervical neoplasia in southern Chinese</title><author>Chan, Paul K.S. ; Cheung, Tak-Hong ; Lin, C. K. ; Siu, Shing-Shun N. ; Yim, So-Fan ; Lo, Keith W.K. ; Cheung, Jo L. K. ; Tam, Ann O.Y. ; Tang, Julian W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5235-b9b1a88941c112cac89feefe8f085ff9b58a37ced49e29fd521c8bd237c4a3343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Asian Continental Ancestry Group - genetics</topic><topic>Biological and medical sciences</topic><topic>Carcinogenesis, carcinogens and anticarcinogens</topic><topic>Case-Control Studies</topic><topic>cervical cancer</topic><topic>Cervical Intraepithelial Neoplasia - genetics</topic><topic>Cervical Intraepithelial Neoplasia - immunology</topic><topic>Cervical Intraepithelial Neoplasia - virology</topic><topic>Chinese</topic><topic>Female</topic><topic>HLA</topic><topic>HLA-DR Antigens - genetics</topic><topic>HLA-DRB1 Chains</topic><topic>Hong Kong</topic><topic>host genetics</topic><topic>HPV</topic><topic>Human papillomavirus</topic><topic>Human papillomavirus 16</topic><topic>Human papillomavirus 16 - genetics</topic><topic>Human papillomavirus 16 - isolation & purification</topic><topic>Human papillomavirus 16 - pathogenicity</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Papillomaviridae - classification</topic><topic>Papillomaviridae - genetics</topic><topic>Papillomaviridae - isolation & purification</topic><topic>Papillomaviridae - pathogenicity</topic><topic>Papillomavirus Infections - genetics</topic><topic>Papillomavirus Infections - immunology</topic><topic>Papillomavirus Infections - virology</topic><topic>Polymorphism, Genetic</topic><topic>Risk Factors</topic><topic>Tumors</topic><topic>Uterine Cervical Neoplasms - genetics</topic><topic>Uterine Cervical Neoplasms - immunology</topic><topic>Uterine Cervical Neoplasms - virology</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chan, Paul K.S.</creatorcontrib><creatorcontrib>Cheung, Tak-Hong</creatorcontrib><creatorcontrib>Lin, C. K.</creatorcontrib><creatorcontrib>Siu, Shing-Shun N.</creatorcontrib><creatorcontrib>Yim, So-Fan</creatorcontrib><creatorcontrib>Lo, Keith W.K.</creatorcontrib><creatorcontrib>Cheung, Jo L. K.</creatorcontrib><creatorcontrib>Tam, Ann O.Y.</creatorcontrib><creatorcontrib>Tang, Julian W.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of medical virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chan, Paul K.S.</au><au>Cheung, Tak-Hong</au><au>Lin, C. K.</au><au>Siu, Shing-Shun N.</au><au>Yim, So-Fan</au><au>Lo, Keith W.K.</au><au>Cheung, Jo L. K.</au><au>Tam, Ann O.Y.</au><au>Tang, Julian W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association Between HLA-DRB1 polymorphism, high-risk HPV infection and cervical neoplasia in southern Chinese</atitle><jtitle>Journal of medical virology</jtitle><addtitle>J. Med. Virol</addtitle><date>2007-07</date><risdate>2007</risdate><volume>79</volume><issue>7</issue><spage>970</spage><epage>976</epage><pages>970-976</pages><issn>0146-6615</issn><eissn>1096-9071</eissn><coden>JMVIDB</coden><abstract>Multiple determinants are involved in the progression of human papillomavirus (HPV)‐infected cervical lesion to invasive cancer. Human leukocyte antigen (HLA) polymorphism seems to play a role. This study examined the association between HLA‐DRB1 polymorphism, high‐risk HPV infection, and the development of cervical neoplasia in southern Chinese. Three hundred and seventy women with cervical neoplasia (43 cervical intraepithelial neoplasia grade II, 154 grade III, and 173 invasive cancers) and 323 controls were recruited for HLA‐DRB1 typing by a sequence‐based approach. Cervical specimens were collected for HPV detection by a consensus primer‐based polymerase chain reaction, and with the type of HPV identified by hybridization with type‐specific oligonucleotide probes. A protective effect of HLA‐DRB1*12 for cervical neoplasia was observed, and with stronger associations when subgroup analyses were carried out for patients infected with HPV16 and HPV58. The protective effect of HLA‐DRB1*13 that had been reported from other populations was not observed. The data obtained in this study showed that HLA‐DRB1*03 conferred a higher risk for HPV18‐infected, but not for HPV16‐, HPV52‐, or HPV58‐infected cervical lesions. Although, HPV52 was reported as uncommon worldwide, it was found to be the second most prevalent type in the southern Chinese population. However, no additional risk association was observed when subgroup analyses were performed for HPV52‐infected patients. The current study shows that, among southern Chinese, the outcome of HPV‐infected cervical lesions is associated with HLA‐DRB1 polymorphism. These associations often vary with the type of HPV infection. J. Med. Virol. 79:970‐976, 2007. © 2007 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>17516530</pmid><doi>10.1002/jmv.20805</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Aged, 80 and over Asian Continental Ancestry Group - genetics Biological and medical sciences Carcinogenesis, carcinogens and anticarcinogens Case-Control Studies cervical cancer Cervical Intraepithelial Neoplasia - genetics Cervical Intraepithelial Neoplasia - immunology Cervical Intraepithelial Neoplasia - virology Chinese Female HLA HLA-DR Antigens - genetics HLA-DRB1 Chains Hong Kong host genetics HPV Human papillomavirus Human papillomavirus 16 Human papillomavirus 16 - genetics Human papillomavirus 16 - isolation & purification Human papillomavirus 16 - pathogenicity Humans Male Medical sciences Middle Aged Papillomaviridae - classification Papillomaviridae - genetics Papillomaviridae - isolation & purification Papillomaviridae - pathogenicity Papillomavirus Infections - genetics Papillomavirus Infections - immunology Papillomavirus Infections - virology Polymorphism, Genetic Risk Factors Tumors Uterine Cervical Neoplasms - genetics Uterine Cervical Neoplasms - immunology Uterine Cervical Neoplasms - virology Viruses |
title | Association Between HLA-DRB1 polymorphism, high-risk HPV infection and cervical neoplasia in southern Chinese |
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