Safety and immunogenicity of multiple conventional immunizations administered during early HIV infection
Twenty-one asymptomatic adults who had recently received multiple polysaccharide, live viral, and protein-derived vaccines were identified as being infected with human immunodeficiency virus (HIV). The mean subject age was 24 years (range 18-33); 20 of 21 (95%) were male. The mean T4 count was 523/m...
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Veröffentlicht in: | Journal of acquired immune deficiency syndromes (1988) 1991, Vol.4 (7), p.724-731 |
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creator | RHOADS, J. L BIRX, D. L WRIGHT, D. C BRUNDAGE, J. F BRANDT, B. L REDFIELD, R. R BURKE, D. S |
description | Twenty-one asymptomatic adults who had recently received multiple polysaccharide, live viral, and protein-derived vaccines were identified as being infected with human immunodeficiency virus (HIV). The mean subject age was 24 years (range 18-33); 20 of 21 (95%) were male. The mean T4 count was 523/mm3 with a mean T4/T8 ratio of 0.6. Serologic responses to immunization with meningococcus group C, adenovirus types 4 and 7, tetanus, and diphtheria were evaluated for the HIV seropositive subjects and were compared with the responses of similarly vaccinated age-, sex-, and race-matched HIV-seronegative controls. Significantly fewer (p less than 0.03) HIV subjects responded to meningococcus C (bactericidal antibody) and adenovirus 4 (neutralizing antibody) vaccines than did normals; the HIV-infected subjects who did respond produced functional antibody comparable to that of normals. Booster responses of HIV subjects to tetanus and diphtheria were comparable to those of normals. HIV-infected vaccine nonresponders did not differ from HIV-infected responders in total white blood cell, T4, T4/T8, total serum IgG, or delayed-type hypersensitivity skin test reactivity. All HIV subjects had negative cultures for live vaccine viruses (rubella, measles, adenovirus, and poliovirus). Postimmunization, no clinically apparent adverse reactions to vaccination were detected. |
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L ; BIRX, D. L ; WRIGHT, D. C ; BRUNDAGE, J. F ; BRANDT, B. L ; REDFIELD, R. R ; BURKE, D. S</creator><creatorcontrib>RHOADS, J. L ; BIRX, D. L ; WRIGHT, D. C ; BRUNDAGE, J. F ; BRANDT, B. L ; REDFIELD, R. R ; BURKE, D. S</creatorcontrib><description>Twenty-one asymptomatic adults who had recently received multiple polysaccharide, live viral, and protein-derived vaccines were identified as being infected with human immunodeficiency virus (HIV). The mean subject age was 24 years (range 18-33); 20 of 21 (95%) were male. The mean T4 count was 523/mm3 with a mean T4/T8 ratio of 0.6. Serologic responses to immunization with meningococcus group C, adenovirus types 4 and 7, tetanus, and diphtheria were evaluated for the HIV seropositive subjects and were compared with the responses of similarly vaccinated age-, sex-, and race-matched HIV-seronegative controls. Significantly fewer (p less than 0.03) HIV subjects responded to meningococcus C (bactericidal antibody) and adenovirus 4 (neutralizing antibody) vaccines than did normals; the HIV-infected subjects who did respond produced functional antibody comparable to that of normals. Booster responses of HIV subjects to tetanus and diphtheria were comparable to those of normals. HIV-infected vaccine nonresponders did not differ from HIV-infected responders in total white blood cell, T4, T4/T8, total serum IgG, or delayed-type hypersensitivity skin test reactivity. All HIV subjects had negative cultures for live vaccine viruses (rubella, measles, adenovirus, and poliovirus). Postimmunization, no clinically apparent adverse reactions to vaccination were detected.</description><identifier>ISSN: 0894-9255</identifier><identifier>EISSN: 2331-2289</identifier><identifier>PMID: 1675680</identifier><language>eng</language><publisher>New York, NY: Raven Press</publisher><subject>Adult ; AIDS/HIV ; Biological and medical sciences ; CD4-Positive T-Lymphocytes - immunology ; Female ; Gene Products, gag - immunology ; HIV Antigens - administration & dosage ; HIV Antigens - immunology ; HIV Antigens - standards ; HIV Core Protein p24 ; HIV Infections - complications ; HIV Infections - prevention & control ; Humans ; Hypersensitivity, Delayed - complications ; Hypersensitivity, Delayed - immunology ; Immunization, Secondary ; Immunopathology ; Leukocyte Count ; Male ; Medical sciences ; Skin Tests ; Viral Core Proteins - immunology ; Viral Vaccines - administration & dosage ; Viral Vaccines - immunology ; Viral Vaccines - standards</subject><ispartof>Journal of acquired immune deficiency syndromes (1988), 1991, Vol.4 (7), p.724-731</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5511823$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1675680$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>RHOADS, J. L</creatorcontrib><creatorcontrib>BIRX, D. L</creatorcontrib><creatorcontrib>WRIGHT, D. C</creatorcontrib><creatorcontrib>BRUNDAGE, J. F</creatorcontrib><creatorcontrib>BRANDT, B. L</creatorcontrib><creatorcontrib>REDFIELD, R. R</creatorcontrib><creatorcontrib>BURKE, D. S</creatorcontrib><title>Safety and immunogenicity of multiple conventional immunizations administered during early HIV infection</title><title>Journal of acquired immune deficiency syndromes (1988)</title><addtitle>J Acquir Immune Defic Syndr (1988)</addtitle><description>Twenty-one asymptomatic adults who had recently received multiple polysaccharide, live viral, and protein-derived vaccines were identified as being infected with human immunodeficiency virus (HIV). The mean subject age was 24 years (range 18-33); 20 of 21 (95%) were male. The mean T4 count was 523/mm3 with a mean T4/T8 ratio of 0.6. Serologic responses to immunization with meningococcus group C, adenovirus types 4 and 7, tetanus, and diphtheria were evaluated for the HIV seropositive subjects and were compared with the responses of similarly vaccinated age-, sex-, and race-matched HIV-seronegative controls. Significantly fewer (p less than 0.03) HIV subjects responded to meningococcus C (bactericidal antibody) and adenovirus 4 (neutralizing antibody) vaccines than did normals; the HIV-infected subjects who did respond produced functional antibody comparable to that of normals. Booster responses of HIV subjects to tetanus and diphtheria were comparable to those of normals. HIV-infected vaccine nonresponders did not differ from HIV-infected responders in total white blood cell, T4, T4/T8, total serum IgG, or delayed-type hypersensitivity skin test reactivity. All HIV subjects had negative cultures for live vaccine viruses (rubella, measles, adenovirus, and poliovirus). Postimmunization, no clinically apparent adverse reactions to vaccination were detected.</description><subject>Adult</subject><subject>AIDS/HIV</subject><subject>Biological and medical sciences</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>Female</subject><subject>Gene Products, gag - immunology</subject><subject>HIV Antigens - administration & dosage</subject><subject>HIV Antigens - immunology</subject><subject>HIV Antigens - standards</subject><subject>HIV Core Protein p24</subject><subject>HIV Infections - complications</subject><subject>HIV Infections - prevention & control</subject><subject>Humans</subject><subject>Hypersensitivity, Delayed - complications</subject><subject>Hypersensitivity, Delayed - immunology</subject><subject>Immunization, Secondary</subject><subject>Immunopathology</subject><subject>Leukocyte Count</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Skin Tests</subject><subject>Viral Core Proteins - immunology</subject><subject>Viral Vaccines - administration & dosage</subject><subject>Viral Vaccines - immunology</subject><subject>Viral Vaccines - standards</subject><issn>0894-9255</issn><issn>2331-2289</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo90E1LxDAQBuAgyrqu_gQhB_FWaJKmSY6yqLuw4MGPa0mTyRpJ09q0wvrr7bLF0zDzPszhPUNLyhjJKJXqHC1zqYpMUc4v0VVKX3nOpRJsgRakFLyU-RJ9vmoHwwHraLFvmjG2e4je-OnUOtyMYfBdAGza-ANx8G3U4eT8rz6uCWvb-OjTAD1YbMfexz0G3YcD3mw_sI8OzBFeowunQ4Kbea7Q-9Pj23qT7V6et-uHXdZRxoeM5Fw4zjlVYHPBoaxrYMqU1FgGFApujOWCKVEY5cAyZ6wxQgMlVFpXFGyF7k9_u779HiENVeOTgRB0hHZMlcxLoqQqJ3g7w7FuwFZd7xvdH6q5mim_m3OdjA6u19H49M84J0ROXf8BeGtwpQ</recordid><startdate>1991</startdate><enddate>1991</enddate><creator>RHOADS, J. L</creator><creator>BIRX, D. L</creator><creator>WRIGHT, D. C</creator><creator>BRUNDAGE, J. F</creator><creator>BRANDT, B. L</creator><creator>REDFIELD, R. R</creator><creator>BURKE, D. S</creator><general>Raven Press</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>1991</creationdate><title>Safety and immunogenicity of multiple conventional immunizations administered during early HIV infection</title><author>RHOADS, J. L ; BIRX, D. L ; WRIGHT, D. C ; BRUNDAGE, J. F ; BRANDT, B. L ; REDFIELD, R. R ; BURKE, D. S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p235t-1057f55529ed075e6bbe39c62cd3e2e45ccd573974c9fed3fcdcc7ae2128df443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Adult</topic><topic>AIDS/HIV</topic><topic>Biological and medical sciences</topic><topic>CD4-Positive T-Lymphocytes - immunology</topic><topic>Female</topic><topic>Gene Products, gag - immunology</topic><topic>HIV Antigens - administration & dosage</topic><topic>HIV Antigens - immunology</topic><topic>HIV Antigens - standards</topic><topic>HIV Core Protein p24</topic><topic>HIV Infections - complications</topic><topic>HIV Infections - prevention & control</topic><topic>Humans</topic><topic>Hypersensitivity, Delayed - complications</topic><topic>Hypersensitivity, Delayed - immunology</topic><topic>Immunization, Secondary</topic><topic>Immunopathology</topic><topic>Leukocyte Count</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Skin Tests</topic><topic>Viral Core Proteins - immunology</topic><topic>Viral Vaccines - administration & dosage</topic><topic>Viral Vaccines - immunology</topic><topic>Viral Vaccines - standards</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>RHOADS, J. L</creatorcontrib><creatorcontrib>BIRX, D. L</creatorcontrib><creatorcontrib>WRIGHT, D. C</creatorcontrib><creatorcontrib>BRUNDAGE, J. F</creatorcontrib><creatorcontrib>BRANDT, B. L</creatorcontrib><creatorcontrib>REDFIELD, R. R</creatorcontrib><creatorcontrib>BURKE, D. S</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>MEDLINE - Academic</collection><jtitle>Journal of acquired immune deficiency syndromes (1988)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>RHOADS, J. L</au><au>BIRX, D. L</au><au>WRIGHT, D. C</au><au>BRUNDAGE, J. F</au><au>BRANDT, B. L</au><au>REDFIELD, R. R</au><au>BURKE, D. S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Safety and immunogenicity of multiple conventional immunizations administered during early HIV infection</atitle><jtitle>Journal of acquired immune deficiency syndromes (1988)</jtitle><addtitle>J Acquir Immune Defic Syndr (1988)</addtitle><date>1991</date><risdate>1991</risdate><volume>4</volume><issue>7</issue><spage>724</spage><epage>731</epage><pages>724-731</pages><issn>0894-9255</issn><eissn>2331-2289</eissn><abstract>Twenty-one asymptomatic adults who had recently received multiple polysaccharide, live viral, and protein-derived vaccines were identified as being infected with human immunodeficiency virus (HIV). The mean subject age was 24 years (range 18-33); 20 of 21 (95%) were male. The mean T4 count was 523/mm3 with a mean T4/T8 ratio of 0.6. Serologic responses to immunization with meningococcus group C, adenovirus types 4 and 7, tetanus, and diphtheria were evaluated for the HIV seropositive subjects and were compared with the responses of similarly vaccinated age-, sex-, and race-matched HIV-seronegative controls. Significantly fewer (p less than 0.03) HIV subjects responded to meningococcus C (bactericidal antibody) and adenovirus 4 (neutralizing antibody) vaccines than did normals; the HIV-infected subjects who did respond produced functional antibody comparable to that of normals. Booster responses of HIV subjects to tetanus and diphtheria were comparable to those of normals. HIV-infected vaccine nonresponders did not differ from HIV-infected responders in total white blood cell, T4, T4/T8, total serum IgG, or delayed-type hypersensitivity skin test reactivity. All HIV subjects had negative cultures for live vaccine viruses (rubella, measles, adenovirus, and poliovirus). Postimmunization, no clinically apparent adverse reactions to vaccination were detected.</abstract><cop>New York, NY</cop><pub>Raven Press</pub><pmid>1675680</pmid><tpages>8</tpages></addata></record> |
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subjects | Adult AIDS/HIV Biological and medical sciences CD4-Positive T-Lymphocytes - immunology Female Gene Products, gag - immunology HIV Antigens - administration & dosage HIV Antigens - immunology HIV Antigens - standards HIV Core Protein p24 HIV Infections - complications HIV Infections - prevention & control Humans Hypersensitivity, Delayed - complications Hypersensitivity, Delayed - immunology Immunization, Secondary Immunopathology Leukocyte Count Male Medical sciences Skin Tests Viral Core Proteins - immunology Viral Vaccines - administration & dosage Viral Vaccines - immunology Viral Vaccines - standards |
title | Safety and immunogenicity of multiple conventional immunizations administered during early HIV infection |
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