Temporal analysis of the antibody response to HIV envelope protein in HIV-infected laboratory workers
Three laboratory workers have been infected with the IIIB strain of HIV; their antibody response to HIV has been studied in serial serum specimens. Because the infecting virus is known, the fine specificity of the antibody response was studied on the homologous strain of HIV. Anti-p17, anti-p24, ant...
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Veröffentlicht in: | The Journal of clinical investigation 1994-06, Vol.93 (6), p.2505-2513 |
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creator | Pincus, S H Messer, K G Nara, P L Blattner, W A Colclough, G Reitz, M |
description | Three laboratory workers have been infected with the IIIB strain of HIV; their antibody response to HIV has been studied in serial serum specimens. Because the infecting virus is known, the fine specificity of the antibody response was studied on the homologous strain of HIV. Anti-p17, anti-p24, anti-gp160, CD4/gp120 blocking and neutralizing antibodies developed in parallel. Epitope mapping of the anti-gp160 response indicated several regions that consistently induced an antibody response. Serum contained antibody which reacted with V3-specific peptides corresponding to the very tip of the loop and crossreactivity was seen with V3 loop peptides from other sequence divergent strains of HIV. Antibody to the V1 loop was produced at levels comparable with that seen for the V3-loop. Anti-V1 neutralized HIV with a titration curve equivalent to an anti-V3 monoclonal antibody. Because the infecting virus is known and serial reisolates have been obtained, we explored the relationship between production of antibody to a given epitope and mutation in the virus. The data suggest that an association exists, but do not clearly indicate that antibody drives the selection for mutant viruses. The findings presented here provide a fine specificity analysis of the evolution of the antibody response to HIV in greater detail than has previously been performed. |
doi_str_mv | 10.1172/JCI117260 |
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Because the infecting virus is known, the fine specificity of the antibody response was studied on the homologous strain of HIV. Anti-p17, anti-p24, anti-gp160, CD4/gp120 blocking and neutralizing antibodies developed in parallel. Epitope mapping of the anti-gp160 response indicated several regions that consistently induced an antibody response. Serum contained antibody which reacted with V3-specific peptides corresponding to the very tip of the loop and crossreactivity was seen with V3 loop peptides from other sequence divergent strains of HIV. Antibody to the V1 loop was produced at levels comparable with that seen for the V3-loop. Anti-V1 neutralized HIV with a titration curve equivalent to an anti-V3 monoclonal antibody. Because the infecting virus is known and serial reisolates have been obtained, we explored the relationship between production of antibody to a given epitope and mutation in the virus. The data suggest that an association exists, but do not clearly indicate that antibody drives the selection for mutant viruses. The findings presented here provide a fine specificity analysis of the evolution of the antibody response to HIV in greater detail than has previously been performed.</description><identifier>ISSN: 0021-9738</identifier><identifier>DOI: 10.1172/JCI117260</identifier><identifier>PMID: 7515393</identifier><language>eng</language><publisher>United States</publisher><subject>Amino Acid Sequence ; Epitopes ; gag Gene Products, Human Immunodeficiency Virus ; Gene Products, env - immunology ; Gene Products, gag - immunology ; HIV Antibodies - blood ; HIV Antigens - immunology ; HIV Core Protein p24 - immunology ; HIV Envelope Protein gp120 - immunology ; HIV Envelope Protein gp160 ; HIV Infections - immunology ; Humans ; Medical Laboratory Personnel ; Molecular Sequence Data ; Occupational Diseases - immunology ; Protein Precursors - immunology ; Viral Proteins</subject><ispartof>The Journal of clinical investigation, 1994-06, Vol.93 (6), p.2505-2513</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c369t-6cb8d73f5e1ea77b95c9dc0668852aa630472554eb617a54666f4532ae1afcd33</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC294468/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC294468/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7515393$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pincus, S H</creatorcontrib><creatorcontrib>Messer, K G</creatorcontrib><creatorcontrib>Nara, P L</creatorcontrib><creatorcontrib>Blattner, W A</creatorcontrib><creatorcontrib>Colclough, G</creatorcontrib><creatorcontrib>Reitz, M</creatorcontrib><title>Temporal analysis of the antibody response to HIV envelope protein in HIV-infected laboratory workers</title><title>The Journal of clinical investigation</title><addtitle>J Clin Invest</addtitle><description>Three laboratory workers have been infected with the IIIB strain of HIV; their antibody response to HIV has been studied in serial serum specimens. Because the infecting virus is known, the fine specificity of the antibody response was studied on the homologous strain of HIV. Anti-p17, anti-p24, anti-gp160, CD4/gp120 blocking and neutralizing antibodies developed in parallel. Epitope mapping of the anti-gp160 response indicated several regions that consistently induced an antibody response. Serum contained antibody which reacted with V3-specific peptides corresponding to the very tip of the loop and crossreactivity was seen with V3 loop peptides from other sequence divergent strains of HIV. Antibody to the V1 loop was produced at levels comparable with that seen for the V3-loop. Anti-V1 neutralized HIV with a titration curve equivalent to an anti-V3 monoclonal antibody. Because the infecting virus is known and serial reisolates have been obtained, we explored the relationship between production of antibody to a given epitope and mutation in the virus. The data suggest that an association exists, but do not clearly indicate that antibody drives the selection for mutant viruses. The findings presented here provide a fine specificity analysis of the evolution of the antibody response to HIV in greater detail than has previously been performed.</description><subject>Amino Acid Sequence</subject><subject>Epitopes</subject><subject>gag Gene Products, Human Immunodeficiency Virus</subject><subject>Gene Products, env - immunology</subject><subject>Gene Products, gag - immunology</subject><subject>HIV Antibodies - blood</subject><subject>HIV Antigens - immunology</subject><subject>HIV Core Protein p24 - immunology</subject><subject>HIV Envelope Protein gp120 - immunology</subject><subject>HIV Envelope Protein gp160</subject><subject>HIV Infections - immunology</subject><subject>Humans</subject><subject>Medical Laboratory Personnel</subject><subject>Molecular Sequence Data</subject><subject>Occupational Diseases - immunology</subject><subject>Protein Precursors - immunology</subject><subject>Viral Proteins</subject><issn>0021-9738</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUMtOwzAQ9AFUSuHAByD5yiFgx6_kwAFVQIMqcSlcI8dZ00AaR7Ypyt-TqlUF0kqj3Z2Z1Q5CV5TcUqrSu5d5sUNJTtCUkJQmuWLZGToP4ZMQyrngEzRRggqWsymCFWx653WLdafbITQBO4vjGsY-NpWrB-wh9K4LgKPDi-IdQ7eF1vWAe-8iNB0ea5wnTWfBRKhxq6vRMTo_4B_nv8CHC3RqdRvg8oAz9Pb0uJovkuXrczF_WCaGyTwm0lRZrZgVQEErVeXC5LUhUmaZSLWWjHCVCsGhklRpwaWUlguWaqDampqxGbrf-_bf1QZqA10cXyt732y0H0qnm_L_pmvW5YfblmnOucxG_c1eb7wLwYM9Sikpd6mWx3RH7vXfW0fmIVr2Czh_eV8</recordid><startdate>19940601</startdate><enddate>19940601</enddate><creator>Pincus, S H</creator><creator>Messer, K G</creator><creator>Nara, P L</creator><creator>Blattner, W A</creator><creator>Colclough, G</creator><creator>Reitz, M</creator><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>5PM</scope></search><sort><creationdate>19940601</creationdate><title>Temporal analysis of the antibody response to HIV envelope protein in HIV-infected laboratory workers</title><author>Pincus, S H ; Messer, K G ; Nara, P L ; Blattner, W A ; Colclough, G ; Reitz, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c369t-6cb8d73f5e1ea77b95c9dc0668852aa630472554eb617a54666f4532ae1afcd33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Amino Acid Sequence</topic><topic>Epitopes</topic><topic>gag Gene Products, Human Immunodeficiency Virus</topic><topic>Gene Products, env - immunology</topic><topic>Gene Products, gag - immunology</topic><topic>HIV Antibodies - blood</topic><topic>HIV Antigens - immunology</topic><topic>HIV Core Protein p24 - immunology</topic><topic>HIV Envelope Protein gp120 - immunology</topic><topic>HIV Envelope Protein gp160</topic><topic>HIV Infections - immunology</topic><topic>Humans</topic><topic>Medical Laboratory Personnel</topic><topic>Molecular Sequence Data</topic><topic>Occupational Diseases - immunology</topic><topic>Protein Precursors - immunology</topic><topic>Viral Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pincus, S H</creatorcontrib><creatorcontrib>Messer, K G</creatorcontrib><creatorcontrib>Nara, P L</creatorcontrib><creatorcontrib>Blattner, W A</creatorcontrib><creatorcontrib>Colclough, G</creatorcontrib><creatorcontrib>Reitz, M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of clinical investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pincus, S H</au><au>Messer, K G</au><au>Nara, P L</au><au>Blattner, W A</au><au>Colclough, G</au><au>Reitz, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Temporal analysis of the antibody response to HIV envelope protein in HIV-infected laboratory workers</atitle><jtitle>The Journal of clinical investigation</jtitle><addtitle>J Clin Invest</addtitle><date>1994-06-01</date><risdate>1994</risdate><volume>93</volume><issue>6</issue><spage>2505</spage><epage>2513</epage><pages>2505-2513</pages><issn>0021-9738</issn><abstract>Three laboratory workers have been infected with the IIIB strain of HIV; their antibody response to HIV has been studied in serial serum specimens. Because the infecting virus is known, the fine specificity of the antibody response was studied on the homologous strain of HIV. Anti-p17, anti-p24, anti-gp160, CD4/gp120 blocking and neutralizing antibodies developed in parallel. Epitope mapping of the anti-gp160 response indicated several regions that consistently induced an antibody response. Serum contained antibody which reacted with V3-specific peptides corresponding to the very tip of the loop and crossreactivity was seen with V3 loop peptides from other sequence divergent strains of HIV. Antibody to the V1 loop was produced at levels comparable with that seen for the V3-loop. Anti-V1 neutralized HIV with a titration curve equivalent to an anti-V3 monoclonal antibody. Because the infecting virus is known and serial reisolates have been obtained, we explored the relationship between production of antibody to a given epitope and mutation in the virus. The data suggest that an association exists, but do not clearly indicate that antibody drives the selection for mutant viruses. The findings presented here provide a fine specificity analysis of the evolution of the antibody response to HIV in greater detail than has previously been performed.</abstract><cop>United States</cop><pmid>7515393</pmid><doi>10.1172/JCI117260</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Sequence Epitopes gag Gene Products, Human Immunodeficiency Virus Gene Products, env - immunology Gene Products, gag - immunology HIV Antibodies - blood HIV Antigens - immunology HIV Core Protein p24 - immunology HIV Envelope Protein gp120 - immunology HIV Envelope Protein gp160 HIV Infections - immunology Humans Medical Laboratory Personnel Molecular Sequence Data Occupational Diseases - immunology Protein Precursors - immunology Viral Proteins |
title | Temporal analysis of the antibody response to HIV envelope protein in HIV-infected laboratory workers |
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