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HIV-1 specific IgA detected in vaginal secretions of HIV uninfected women participating in a microbicide trial in Southern Africa are primarily directed toward gp120 and gp140 specificities.

Identifieur interne : 002A93 ( PubMed/Checkpoint ); précédent : 002A92; suivant : 002A94

HIV-1 specific IgA detected in vaginal secretions of HIV uninfected women participating in a microbicide trial in Southern Africa are primarily directed toward gp120 and gp140 specificities.

Auteurs : Kelly E. Seaton [États-Unis] ; Lamar Ballweber [États-Unis] ; Audrey Lan [États-Unis] ; Michele Donathan [États-Unis] ; Sean Hughes [États-Unis] ; Lucia Vojtech [États-Unis] ; M Anthony Moody [États-Unis] ; Hua-Xin Liao [États-Unis] ; Barton F. Haynes [États-Unis] ; Christine G. Galloway [États-Unis] ; Barbra A. Richardson [États-Unis] ; Salim Abdool Karim [États-Unis] ; Charlene S. Dezzutti [États-Unis] ; M Juliana Mcelrath [États-Unis] ; Georgia D. Tomaras [États-Unis] ; Florian Hladik [États-Unis]

Source :

RBID : pubmed:25054205

Descripteurs français

English descriptors

Abstract

Many participants in microbicide trials remain uninfected despite ongoing exposure to HIV-1. Determining the emergence and nature of mucosal HIV-specific immune responses in such women is important, since these responses may contribute to protection and could provide insight for the rational design of HIV-1 vaccines.

DOI: 10.1371/journal.pone.0101863
PubMed: 25054205


Affiliations:


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pubmed:25054205

Le document en format XML

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<date when="2014" type="published">2014</date>
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<keywords scheme="KwdEn" xml:lang="en">
<term>Analysis of Variance</term>
<term>Anti-Infective Agents (immunology)</term>
<term>Anti-Infective Agents (therapeutic use)</term>
<term>Bodily Secretions (immunology)</term>
<term>Bodily Secretions (virology)</term>
<term>Cohort Studies</term>
<term>Female</term>
<term>HIV Antibodies (immunology)</term>
<term>HIV Envelope Protein gp120 (immunology)</term>
<term>HIV Infections (diagnosis)</term>
<term>HIV Infections (immunology)</term>
<term>HIV Infections (prevention & control)</term>
<term>HIV Seronegativity (immunology)</term>
<term>HIV Seropositivity (immunology)</term>
<term>HIV-1 (drug effects)</term>
<term>HIV-1 (immunology)</term>
<term>Humans</term>
<term>Immunity, Mucosal (drug effects)</term>
<term>Immunity, Mucosal (immunology)</term>
<term>Immunoglobulin A (immunology)</term>
<term>Immunoglobulin G (immunology)</term>
<term>Pilot Projects</term>
<term>South Africa</term>
<term>Specimen Handling (instrumentation)</term>
<term>Specimen Handling (methods)</term>
<term>Vagina (immunology)</term>
<term>Vagina (virology)</term>
<term>env Gene Products, Human Immunodeficiency Virus (immunology)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Analyse de variance</term>
<term>Anti-infectieux (immunologie)</term>
<term>Anti-infectieux (usage thérapeutique)</term>
<term>Anticorps anti-VIH (immunologie)</term>
<term>Femelle</term>
<term>Humains</term>
<term>Immunité muqueuse ()</term>
<term>Immunité muqueuse (immunologie)</term>
<term>Immunoglobuline A (immunologie)</term>
<term>Immunoglobuline G (immunologie)</term>
<term>Infections à VIH ()</term>
<term>Infections à VIH (diagnostic)</term>
<term>Infections à VIH (immunologie)</term>
<term>Produits du gène env du virus de l'immunodéficience humaine (immunologie)</term>
<term>Projets pilotes</term>
<term>Protéine d'enveloppe gp120 du VIH (immunologie)</term>
<term>Prélèvement biologique ()</term>
<term>Prélèvement biologique (instrumentation)</term>
<term>République d'Afrique du Sud</term>
<term>Sécrétions corporelles (immunologie)</term>
<term>Sécrétions corporelles (virologie)</term>
<term>Séronégativité VIH (immunologie)</term>
<term>Séropositivité VIH (immunologie)</term>
<term>VIH-1 (Virus de l'Immunodéficience Humaine de type 1) ()</term>
<term>VIH-1 (Virus de l'Immunodéficience Humaine de type 1) (immunologie)</term>
<term>Vagin (immunologie)</term>
<term>Vagin (virologie)</term>
<term>Études de cohortes</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="immunology" xml:lang="en">
<term>Anti-Infective Agents</term>
<term>HIV Antibodies</term>
<term>HIV Envelope Protein gp120</term>
<term>Immunoglobulin A</term>
<term>Immunoglobulin G</term>
<term>env Gene Products, Human Immunodeficiency Virus</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en">
<term>Anti-Infective Agents</term>
</keywords>
<keywords scheme="MESH" type="geographic" xml:lang="en">
<term>South Africa</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en">
<term>HIV Infections</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr">
<term>Infections à VIH</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en">
<term>HIV-1</term>
<term>Immunity, Mucosal</term>
</keywords>
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<term>Anti-infectieux</term>
<term>Anticorps anti-VIH</term>
<term>Immunité muqueuse</term>
<term>Immunoglobuline A</term>
<term>Immunoglobuline G</term>
<term>Infections à VIH</term>
<term>Produits du gène env du virus de l'immunodéficience humaine</term>
<term>Protéine d'enveloppe gp120 du VIH</term>
<term>Sécrétions corporelles</term>
<term>Séronégativité VIH</term>
<term>Séropositivité VIH</term>
<term>VIH-1 (Virus de l'Immunodéficience Humaine de type 1)</term>
<term>Vagin</term>
</keywords>
<keywords scheme="MESH" qualifier="immunology" xml:lang="en">
<term>Bodily Secretions</term>
<term>HIV Infections</term>
<term>HIV Seronegativity</term>
<term>HIV Seropositivity</term>
<term>HIV-1</term>
<term>Immunity, Mucosal</term>
<term>Vagina</term>
</keywords>
<keywords scheme="MESH" qualifier="instrumentation" xml:lang="en">
<term>Specimen Handling</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en">
<term>Specimen Handling</term>
</keywords>
<keywords scheme="MESH" qualifier="prevention & control" xml:lang="en">
<term>HIV Infections</term>
</keywords>
<keywords scheme="MESH" qualifier="usage thérapeutique" xml:lang="fr">
<term>Anti-infectieux</term>
<term>Prélèvement biologique</term>
</keywords>
<keywords scheme="MESH" qualifier="virologie" xml:lang="fr">
<term>Sécrétions corporelles</term>
<term>Vagin</term>
</keywords>
<keywords scheme="MESH" qualifier="virology" xml:lang="en">
<term>Bodily Secretions</term>
<term>Vagina</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Analysis of Variance</term>
<term>Cohort Studies</term>
<term>Female</term>
<term>Humans</term>
<term>Pilot Projects</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Analyse de variance</term>
<term>Femelle</term>
<term>Humains</term>
<term>Immunité muqueuse</term>
<term>Infections à VIH</term>
<term>Projets pilotes</term>
<term>Prélèvement biologique</term>
<term>République d'Afrique du Sud</term>
<term>VIH-1 (Virus de l'Immunodéficience Humaine de type 1)</term>
<term>Études de cohortes</term>
</keywords>
<keywords scheme="Wicri" type="geographic" xml:lang="fr">
<term>Afrique du Sud</term>
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<front>
<div type="abstract" xml:lang="en">Many participants in microbicide trials remain uninfected despite ongoing exposure to HIV-1. Determining the emergence and nature of mucosal HIV-specific immune responses in such women is important, since these responses may contribute to protection and could provide insight for the rational design of HIV-1 vaccines.</div>
</front>
</TEI>
<pubmed>
<MedlineCitation Status="MEDLINE" Owner="NLM">
<PMID Version="1">25054205</PMID>
<DateCreated>
<Year>2014</Year>
<Month>07</Month>
<Day>24</Day>
</DateCreated>
<DateCompleted>
<Year>2015</Year>
<Month>04</Month>
<Day>20</Day>
</DateCompleted>
<DateRevised>
<Year>2016</Year>
<Month>12</Month>
<Day>15</Day>
</DateRevised>
<Article PubModel="Electronic-eCollection">
<Journal>
<ISSN IssnType="Electronic">1932-6203</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>9</Volume>
<Issue>7</Issue>
<PubDate>
<Year>2014</Year>
</PubDate>
</JournalIssue>
<Title>PloS one</Title>
<ISOAbbreviation>PLoS ONE</ISOAbbreviation>
</Journal>
<ArticleTitle>HIV-1 specific IgA detected in vaginal secretions of HIV uninfected women participating in a microbicide trial in Southern Africa are primarily directed toward gp120 and gp140 specificities.</ArticleTitle>
<Pagination>
<MedlinePgn>e101863</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1371/journal.pone.0101863</ELocationID>
<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Many participants in microbicide trials remain uninfected despite ongoing exposure to HIV-1. Determining the emergence and nature of mucosal HIV-specific immune responses in such women is important, since these responses may contribute to protection and could provide insight for the rational design of HIV-1 vaccines.</AbstractText>
<AbstractText Label="METHODS AND FINDINGS" NlmCategory="RESULTS">We first conducted a pilot study to compare three sampling devices (Dacron swabs, flocked nylon swabs and Merocel sponges) for detection of HIV-1-specific IgG and IgA antibodies in vaginal secretions. IgG antibodies from HIV-1-positive women reacted broadly across the full panel of eight HIV-1 envelope (Env) antigens tested, whereas IgA antibodies only reacted to the gp41 subunit. No Env-reactive antibodies were detected in the HIV-negative women. The three sampling devices yielded equal HIV-1-specific antibody titers, as well as total IgG and IgA concentrations. We then tested vaginal Dacron swabs archived from 57 HIV seronegative women who participated in a microbicide efficacy trial in Southern Africa (HPTN 035). We detected vaginal IgA antibodies directed at HIV-1 Env gp120/gp140 in six of these women, and at gp41 in another three women, but did not detect Env-specific IgG antibodies in any women.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Vaginal secretions of HIV-1 infected women contained IgG reactivity to a broad range of Env antigens and IgA reactivity to gp41. In contrast, Env-binding antibodies in the vaginal secretions of HIV-1 uninfected women participating in the microbicide trial were restricted to the IgA subtype and were mostly directed at HIV-1 gp120/gp140.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Seaton</LastName>
<ForeName>Kelly E</ForeName>
<Initials>KE</Initials>
<AffiliationInfo>
<Affiliation>Duke Human Vaccine Institute, Durham, North Carolina, United States of America.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Ballweber</LastName>
<ForeName>Lamar</ForeName>
<Initials>L</Initials>
<AffiliationInfo>
<Affiliation>Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington, United States of America.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Lan</LastName>
<ForeName>Audrey</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Duke Human Vaccine Institute, Durham, North Carolina, United States of America.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Donathan</LastName>
<ForeName>Michele</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>Duke Human Vaccine Institute, Durham, North Carolina, United States of America.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Hughes</LastName>
<ForeName>Sean</ForeName>
<Initials>S</Initials>
<AffiliationInfo>
<Affiliation>Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington, United States of America.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Vojtech</LastName>
<ForeName>Lucia</ForeName>
<Initials>L</Initials>
<AffiliationInfo>
<Affiliation>Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington, United States of America.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Moody</LastName>
<ForeName>M Anthony</ForeName>
<Initials>MA</Initials>
<AffiliationInfo>
<Affiliation>Duke Human Vaccine Institute, Durham, North Carolina, United States of America.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Liao</LastName>
<ForeName>Hua-Xin</ForeName>
<Initials>HX</Initials>
<AffiliationInfo>
<Affiliation>Duke Human Vaccine Institute, Durham, North Carolina, United States of America.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Haynes</LastName>
<ForeName>Barton F</ForeName>
<Initials>BF</Initials>
<AffiliationInfo>
<Affiliation>Duke Human Vaccine Institute, Durham, North Carolina, United States of America.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Galloway</LastName>
<ForeName>Christine G</ForeName>
<Initials>CG</Initials>
<AffiliationInfo>
<Affiliation>Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Richardson</LastName>
<ForeName>Barbra A</ForeName>
<Initials>BA</Initials>
<AffiliationInfo>
<Affiliation>Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America; Department of Biostatistics, University of Washington, Seattle, Washington, United States of America.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Karim</LastName>
<ForeName>Salim Abdool</ForeName>
<Initials>SA</Initials>
<AffiliationInfo>
<Affiliation>CAPRISA - Centre for the AIDS Programme of Research in South Africa, Nelson R Mandela School of Medicine, University of KwaZulu-Natal, Durban, South Africa; Department of Epidemiology, Columbia University, New York, New York, United States of America.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Dezzutti</LastName>
<ForeName>Charlene S</ForeName>
<Initials>CS</Initials>
<AffiliationInfo>
<Affiliation>Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, United States of America.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>McElrath</LastName>
<ForeName>M Juliana</ForeName>
<Initials>MJ</Initials>
<AffiliationInfo>
<Affiliation>Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America; Department of Medicine, University of Washington, Seattle, Washington, United States of America; Department of Laboratory Medicine, University of Washington, Seattle, Washington, United States of America; Department of Global Health, University of Washington, Seattle, Washington, United States of America.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Tomaras</LastName>
<ForeName>Georgia D</ForeName>
<Initials>GD</Initials>
<AffiliationInfo>
<Affiliation>Duke Human Vaccine Institute, Durham, North Carolina, United States of America.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Hladik</LastName>
<ForeName>Florian</ForeName>
<Initials>F</Initials>
<AffiliationInfo>
<Affiliation>Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington, United States of America; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America; Department of Medicine, University of Washington, Seattle, Washington, United States of America.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<GrantList CompleteYN="Y">
<Grant>
<GrantID>UL1 TR000005</GrantID>
<Acronym>TR</Acronym>
<Agency>NCATS NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant>
<GrantID>UM1 AI068633</GrantID>
<Acronym>AI</Acronym>
<Agency>NIAID NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant>
<GrantID>P30AI064518</GrantID>
<Acronym>AI</Acronym>
<Agency>NIAID NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant>
<GrantID>U19AI067854</GrantID>
<Acronym>AI</Acronym>
<Agency>NIAID NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant>
<GrantID>UM1 AI068615</GrantID>
<Acronym>AI</Acronym>
<Agency>NIAID NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant>
<GrantID>UM1 AI106707</GrantID>
<Acronym>AI</Acronym>
<Agency>NIAID NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant>
<GrantID>UM1 AI069481</GrantID>
<Acronym>AI</Acronym>
<Agency>NIAID NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant>
<GrantID>UM1 AI068618</GrantID>
<Acronym>AI</Acronym>
<Agency>NIAID NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant>
<GrantID>UM1AI068618</GrantID>
<Acronym>AI</Acronym>
<Agency>NIAID NIH HHS</Agency>
<Country>United States</Country>
</Grant>
</GrantList>
<PublicationTypeList>
<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D052061">Research Support, N.I.H., Extramural</PublicationType>
<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic">
<Year>2014</Year>
<Month>07</Month>
<Day>23</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo>
<Country>United States</Country>
<MedlineTA>PLoS One</MedlineTA>
<NlmUniqueID>101285081</NlmUniqueID>
<ISSNLinking>1932-6203</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D000890">Anti-Infective Agents</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D015483">HIV Antibodies</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D015699">HIV Envelope Protein gp120</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D007070">Immunoglobulin A</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D007074">Immunoglobulin G</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D054299">env Gene Products, Human Immunodeficiency Virus</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="C097729">gp140 envelope protein, Human immunodeficiency virus 1</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
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<MeshHeading>
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<MeshHeading>
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<name sortKey="Vojtech, Lucia" sort="Vojtech, Lucia" uniqKey="Vojtech L" first="Lucia" last="Vojtech">Lucia Vojtech</name>
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