Human papillomavirus type 16 E6/E7‐specific cytotoxic T lymphocytes in women with cervical neoplasia
Infection with oncogenic human papillomavirus (HPV) types is associated with the development of cervical neoplasia (CIN). The E6 and E7 oncoproteins are constitutively expressed in these lesions and are therefore putative targets for the immune response against HPV. The relation between HPV 16‐speci...
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creator | Bontkes, Hetty J. de Gruijl, Tanja D. van den Muysenberg, Adrie J.C. Verheijen, René H.M. Stukart, Marij J. Meijer, Chris J.L.M. Scheper, Rik J. Stacey, Simon N. Duggan‐Keen, Margaret F. Stern, Peter L. Man, Stephen Borysiewicz, Leszek K. Walboomers, Jan M.M. |
description | Infection with oncogenic human papillomavirus (HPV) types is associated with the development of cervical neoplasia (CIN). The E6 and E7 oncoproteins are constitutively expressed in these lesions and are therefore putative targets for the immune response against HPV. The relation between HPV 16‐specific memory cytotoxic T‐cell precursor (mCTLp) activity to both oncoproteins and the natural course of cervical dysplasia was analyzed in 38 patients participating in a nonintervention cohort study of women with CIN and 11 HPV 16‐positive cervical carcinoma patients. In a cross‐sectional study at the end of follow‐up prior to biopsy, 8 of 20 patients with a persistent HPV 16 infection had specific mCTLp against at least one of the two oncoproteins. By contrast, no specific mCTLp activity was detected in 11 HPV‐negative patients or in 7 patients who had cleared an HPV 16 infection at the end of follow‐up. However, 5 of 11 cervical carcinoma patients showed mCTLp activity against the E7 protein only. This study demonstrates that HPV 16 oncogene‐specific mCTLp are present in women with HPV 16‐positive CIN prior to any intervention. Since HPV‐specific mCTLp were detected predominantly in women with high‐grade lesions or invasive cervical carcinoma and not in women who cleared the virus, the role of naturally occurring mCTLp in the protection against HPV‐associated cervical neoplasia remains to be established. Int. J. Cancer 88:92–98, 2000. © 2000 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/1097-0215(20001001)88:1<92::AID-IJC15>3.0.CO;2-E |
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The E6 and E7 oncoproteins are constitutively expressed in these lesions and are therefore putative targets for the immune response against HPV. The relation between HPV 16‐specific memory cytotoxic T‐cell precursor (mCTLp) activity to both oncoproteins and the natural course of cervical dysplasia was analyzed in 38 patients participating in a nonintervention cohort study of women with CIN and 11 HPV 16‐positive cervical carcinoma patients. In a cross‐sectional study at the end of follow‐up prior to biopsy, 8 of 20 patients with a persistent HPV 16 infection had specific mCTLp against at least one of the two oncoproteins. By contrast, no specific mCTLp activity was detected in 11 HPV‐negative patients or in 7 patients who had cleared an HPV 16 infection at the end of follow‐up. However, 5 of 11 cervical carcinoma patients showed mCTLp activity against the E7 protein only. This study demonstrates that HPV 16 oncogene‐specific mCTLp are present in women with HPV 16‐positive CIN prior to any intervention. Since HPV‐specific mCTLp were detected predominantly in women with high‐grade lesions or invasive cervical carcinoma and not in women who cleared the virus, the role of naturally occurring mCTLp in the protection against HPV‐associated cervical neoplasia remains to be established. Int. J. Cancer 88:92–98, 2000. © 2000 Wiley‐Liss, Inc.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/1097-0215(20001001)88:1<92::AID-IJC15>3.0.CO;2-E</identifier><identifier>PMID: 10962445</identifier><identifier>CODEN: IJCNAW</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>Biological and medical sciences ; Cervical Intraepithelial Neoplasia - immunology ; Cervical Intraepithelial Neoplasia - virology ; Cohort Studies ; Cross-Sectional Studies ; Female ; Female genital diseases ; Gynecology. Andrology. Obstetrics ; Humans ; Immunologic Memory - immunology ; Interleukin-2 - biosynthesis ; Interleukin-2 - secretion ; Lymphocyte Activation - immunology ; Medical sciences ; Middle Aged ; Oncogene Proteins, Viral - immunology ; Papillomaviridae - immunology ; Papillomavirus Infections - immunology ; Papillomavirus Infections - virology ; Repressor Proteins ; T-Lymphocytes, Cytotoxic - immunology ; T-Lymphocytes, Helper-Inducer - immunology ; Tumor Virus Infections - immunology ; Tumor Virus Infections - virology ; Tumors ; Uterine Cervical Neoplasms - immunology ; Uterine Cervical Neoplasms - virology</subject><ispartof>International journal of cancer, 2000-10, Vol.88 (1), p.92-98</ispartof><rights>Copyright © 2000 Wiley‐Liss, Inc.</rights><rights>2000 INIST-CNRS</rights><rights>Copyright 2000 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3845-f36563a4f3e5b040f33edb2cff39a0e4fc3316f490bc79687868e82111b22c8d3</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%2F1097-0215%2820001001%2988%3A1%3C92%3A%3AAID-IJC15%3E3.0.CO%3B2-E$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F1097-0215%2820001001%2988%3A1%3C92%3A%3AAID-IJC15%3E3.0.CO%3B2-E$$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=1498138$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10962445$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bontkes, Hetty J.</creatorcontrib><creatorcontrib>de Gruijl, Tanja D.</creatorcontrib><creatorcontrib>van den Muysenberg, Adrie J.C.</creatorcontrib><creatorcontrib>Verheijen, René H.M.</creatorcontrib><creatorcontrib>Stukart, Marij J.</creatorcontrib><creatorcontrib>Meijer, Chris J.L.M.</creatorcontrib><creatorcontrib>Scheper, Rik J.</creatorcontrib><creatorcontrib>Stacey, Simon N.</creatorcontrib><creatorcontrib>Duggan‐Keen, Margaret F.</creatorcontrib><creatorcontrib>Stern, Peter L.</creatorcontrib><creatorcontrib>Man, Stephen</creatorcontrib><creatorcontrib>Borysiewicz, Leszek K.</creatorcontrib><creatorcontrib>Walboomers, Jan M.M.</creatorcontrib><title>Human papillomavirus type 16 E6/E7‐specific cytotoxic T lymphocytes in women with cervical neoplasia</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>Infection with oncogenic human papillomavirus (HPV) types is associated with the development of cervical neoplasia (CIN). The E6 and E7 oncoproteins are constitutively expressed in these lesions and are therefore putative targets for the immune response against HPV. The relation between HPV 16‐specific memory cytotoxic T‐cell precursor (mCTLp) activity to both oncoproteins and the natural course of cervical dysplasia was analyzed in 38 patients participating in a nonintervention cohort study of women with CIN and 11 HPV 16‐positive cervical carcinoma patients. In a cross‐sectional study at the end of follow‐up prior to biopsy, 8 of 20 patients with a persistent HPV 16 infection had specific mCTLp against at least one of the two oncoproteins. By contrast, no specific mCTLp activity was detected in 11 HPV‐negative patients or in 7 patients who had cleared an HPV 16 infection at the end of follow‐up. However, 5 of 11 cervical carcinoma patients showed mCTLp activity against the E7 protein only. This study demonstrates that HPV 16 oncogene‐specific mCTLp are present in women with HPV 16‐positive CIN prior to any intervention. Since HPV‐specific mCTLp were detected predominantly in women with high‐grade lesions or invasive cervical carcinoma and not in women who cleared the virus, the role of naturally occurring mCTLp in the protection against HPV‐associated cervical neoplasia remains to be established. Int. J. Cancer 88:92–98, 2000. © 2000 Wiley‐Liss, Inc.</description><subject>Biological and medical sciences</subject><subject>Cervical Intraepithelial Neoplasia - immunology</subject><subject>Cervical Intraepithelial Neoplasia - virology</subject><subject>Cohort Studies</subject><subject>Cross-Sectional Studies</subject><subject>Female</subject><subject>Female genital diseases</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Immunologic Memory - immunology</subject><subject>Interleukin-2 - biosynthesis</subject><subject>Interleukin-2 - secretion</subject><subject>Lymphocyte Activation - immunology</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Oncogene Proteins, Viral - immunology</subject><subject>Papillomaviridae - immunology</subject><subject>Papillomavirus Infections - immunology</subject><subject>Papillomavirus Infections - virology</subject><subject>Repressor Proteins</subject><subject>T-Lymphocytes, Cytotoxic - immunology</subject><subject>T-Lymphocytes, Helper-Inducer - immunology</subject><subject>Tumor Virus Infections - immunology</subject><subject>Tumor Virus Infections - virology</subject><subject>Tumors</subject><subject>Uterine Cervical Neoplasms - immunology</subject><subject>Uterine Cervical Neoplasms - virology</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkM1u1DAURi0EokPhFZAXCMEiU1_bSZwBIVUh0EGVBqGyvvJ4bNUomYQ4acmOR-AZeRI8ZPhZsGFjW1fnfv50CFHAlsAYPwNW5AnjkD7jjLE4gudKreBlwVer8_XrZP2uhPSVWLJluXnBk-oOWfxeuUsWMYIlOYjshDwI4VNch5TJ--QkQhmXMl0QdzE2ek873fm6bht94_sx0GHqLIWMVtlZlX__-i101njnDTXT0A7tl_i6ovXUdNdtnNhA_Z7eto2Npx-uqbH9jTe6pnvbdrUOXj8k95yug310vE_JxzfVVXmRXG7ersvzy8QIJdPEiSzNhJZO2HTLJHNC2N2WG-dEoZmVzggBmZMF25q8yFSuMmUVB4At50btxCl5Oud2fft5tGHAxgdj61rHKmPAnHOQwCGC72fQ9G0IvXXY9b7R_YTA8OAeDyLxIBJ_uUelELDgiNE9_nSPAhmWG-RYxcjHx7_HbWN3fwXOsiPw5AjoEO24Xu-ND384WSgQKmIfZuzW13b6n17_qjUPxA9bWKlC</recordid><startdate>20001001</startdate><enddate>20001001</enddate><creator>Bontkes, Hetty J.</creator><creator>de Gruijl, Tanja D.</creator><creator>van den Muysenberg, Adrie J.C.</creator><creator>Verheijen, René H.M.</creator><creator>Stukart, Marij J.</creator><creator>Meijer, Chris J.L.M.</creator><creator>Scheper, Rik J.</creator><creator>Stacey, Simon N.</creator><creator>Duggan‐Keen, Margaret F.</creator><creator>Stern, Peter L.</creator><creator>Man, Stephen</creator><creator>Borysiewicz, Leszek K.</creator><creator>Walboomers, Jan M.M.</creator><general>John Wiley & Sons, Inc</general><general>Wiley-Liss</general><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>7X8</scope></search><sort><creationdate>20001001</creationdate><title>Human papillomavirus type 16 E6/E7‐specific cytotoxic T lymphocytes in women with cervical neoplasia</title><author>Bontkes, Hetty J. ; de Gruijl, Tanja D. ; van den Muysenberg, Adrie J.C. ; Verheijen, René H.M. ; Stukart, Marij J. ; Meijer, Chris J.L.M. ; Scheper, Rik J. ; Stacey, Simon N. ; Duggan‐Keen, Margaret F. ; Stern, Peter L. ; Man, Stephen ; Borysiewicz, Leszek K. ; Walboomers, Jan M.M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3845-f36563a4f3e5b040f33edb2cff39a0e4fc3316f490bc79687868e82111b22c8d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Biological and medical sciences</topic><topic>Cervical Intraepithelial Neoplasia - immunology</topic><topic>Cervical Intraepithelial Neoplasia - virology</topic><topic>Cohort Studies</topic><topic>Cross-Sectional Studies</topic><topic>Female</topic><topic>Female genital diseases</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Immunologic Memory - immunology</topic><topic>Interleukin-2 - biosynthesis</topic><topic>Interleukin-2 - secretion</topic><topic>Lymphocyte Activation - immunology</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Oncogene Proteins, Viral - immunology</topic><topic>Papillomaviridae - immunology</topic><topic>Papillomavirus Infections - immunology</topic><topic>Papillomavirus Infections - virology</topic><topic>Repressor Proteins</topic><topic>T-Lymphocytes, Cytotoxic - immunology</topic><topic>T-Lymphocytes, Helper-Inducer - immunology</topic><topic>Tumor Virus Infections - immunology</topic><topic>Tumor Virus Infections - virology</topic><topic>Tumors</topic><topic>Uterine Cervical Neoplasms - immunology</topic><topic>Uterine Cervical Neoplasms - virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bontkes, Hetty J.</creatorcontrib><creatorcontrib>de Gruijl, Tanja D.</creatorcontrib><creatorcontrib>van den Muysenberg, Adrie J.C.</creatorcontrib><creatorcontrib>Verheijen, René H.M.</creatorcontrib><creatorcontrib>Stukart, Marij J.</creatorcontrib><creatorcontrib>Meijer, Chris J.L.M.</creatorcontrib><creatorcontrib>Scheper, Rik J.</creatorcontrib><creatorcontrib>Stacey, Simon N.</creatorcontrib><creatorcontrib>Duggan‐Keen, Margaret F.</creatorcontrib><creatorcontrib>Stern, Peter L.</creatorcontrib><creatorcontrib>Man, Stephen</creatorcontrib><creatorcontrib>Borysiewicz, Leszek K.</creatorcontrib><creatorcontrib>Walboomers, Jan M.M.</creatorcontrib><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>MEDLINE - Academic</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bontkes, Hetty J.</au><au>de Gruijl, Tanja D.</au><au>van den Muysenberg, Adrie J.C.</au><au>Verheijen, René H.M.</au><au>Stukart, Marij J.</au><au>Meijer, Chris J.L.M.</au><au>Scheper, Rik J.</au><au>Stacey, Simon N.</au><au>Duggan‐Keen, Margaret F.</au><au>Stern, Peter L.</au><au>Man, Stephen</au><au>Borysiewicz, Leszek K.</au><au>Walboomers, Jan M.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human papillomavirus type 16 E6/E7‐specific cytotoxic T lymphocytes in women with cervical neoplasia</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>2000-10-01</date><risdate>2000</risdate><volume>88</volume><issue>1</issue><spage>92</spage><epage>98</epage><pages>92-98</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><coden>IJCNAW</coden><abstract>Infection with oncogenic human papillomavirus (HPV) types is associated with the development of cervical neoplasia (CIN). The E6 and E7 oncoproteins are constitutively expressed in these lesions and are therefore putative targets for the immune response against HPV. The relation between HPV 16‐specific memory cytotoxic T‐cell precursor (mCTLp) activity to both oncoproteins and the natural course of cervical dysplasia was analyzed in 38 patients participating in a nonintervention cohort study of women with CIN and 11 HPV 16‐positive cervical carcinoma patients. In a cross‐sectional study at the end of follow‐up prior to biopsy, 8 of 20 patients with a persistent HPV 16 infection had specific mCTLp against at least one of the two oncoproteins. By contrast, no specific mCTLp activity was detected in 11 HPV‐negative patients or in 7 patients who had cleared an HPV 16 infection at the end of follow‐up. However, 5 of 11 cervical carcinoma patients showed mCTLp activity against the E7 protein only. This study demonstrates that HPV 16 oncogene‐specific mCTLp are present in women with HPV 16‐positive CIN prior to any intervention. Since HPV‐specific mCTLp were detected predominantly in women with high‐grade lesions or invasive cervical carcinoma and not in women who cleared the virus, the role of naturally occurring mCTLp in the protection against HPV‐associated cervical neoplasia remains to be established. Int. J. Cancer 88:92–98, 2000. © 2000 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>10962445</pmid><doi>10.1002/1097-0215(20001001)88:1<92::AID-IJC15>3.0.CO;2-E</doi><tpages>7</tpages></addata></record> |
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subjects | Biological and medical sciences Cervical Intraepithelial Neoplasia - immunology Cervical Intraepithelial Neoplasia - virology Cohort Studies Cross-Sectional Studies Female Female genital diseases Gynecology. Andrology. Obstetrics Humans Immunologic Memory - immunology Interleukin-2 - biosynthesis Interleukin-2 - secretion Lymphocyte Activation - immunology Medical sciences Middle Aged Oncogene Proteins, Viral - immunology Papillomaviridae - immunology Papillomavirus Infections - immunology Papillomavirus Infections - virology Repressor Proteins T-Lymphocytes, Cytotoxic - immunology T-Lymphocytes, Helper-Inducer - immunology Tumor Virus Infections - immunology Tumor Virus Infections - virology Tumors Uterine Cervical Neoplasms - immunology Uterine Cervical Neoplasms - virology |
title | Human papillomavirus type 16 E6/E7‐specific cytotoxic T lymphocytes in women with cervical neoplasia |
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