rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2004-3-1
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pubmed:abstractText |
The high prevalence of preexisting immunity to adenovirus serotype 5 (Ad5) in human populations will likely limit the immunogenicity and clinical utility of recombinant Ad5 vector-based vaccines for human immunodeficiency virus type 1 and other pathogens. Ad5-specific neutralizing antibodies (NAbs) are thought to contribute substantially to anti-Ad5 immunity, but the potential importance of Ad5-specific T lymphocytes in this setting has not been fully characterized. Here we assess the relative contributions of Ad5-specific humoral and cellular immune responses in blunting the immunogenicity of a rAd5-Env vaccine in mice. Adoptive transfer of Ad5-specific NAbs resulted in a dramatic abrogation of Env-specific immune responses following immunization with rAd5-Env. Interestingly, adoptive transfer of Ad5-specific CD8(+) T lymphocytes also resulted in a significant and durable suppression of rAd5-Env immunogenicity. These data demonstrate that NAbs and CD8(+) T lymphocytes both contribute to immunity to Ad5. Novel adenovirus vectors that are currently being developed to circumvent the problem of preexisting anti-Ad5 immunity should therefore be designed to evade both humoral and cellular Ad5-specific immune responses.
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pubmed:grant |
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/14990686-10400791,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14990686-10906225,
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0022-538X
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pubmed:author |
pubmed-author:ArthurJanelle CJC,
pubmed-author:BarouchDan HDH,
pubmed-author:GorgoneDarci ADA,
pubmed-author:GoudsmitJaapJ,
pubmed-author:HavengaMenzo J EMJ,
pubmed-author:JacksonShawn SSS,
pubmed-author:KishkoMichael GMG,
pubmed-author:KostenseStefanS,
pubmed-author:KoudstaalWouterW,
pubmed-author:LetvinNorman LNL,
pubmed-author:LiftonMichelle AMA,
pubmed-author:PauMaria GMG,
pubmed-author:SumidaShawn MSM,
pubmed-author:TruittDiana MDM
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pubmed:issnType |
Print
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pubmed:volume |
78
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2666-73
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:14990686-Adenovirus Infections, Human,
pubmed-meshheading:14990686-Adenoviruses, Human,
pubmed-meshheading:14990686-Adoptive Transfer,
pubmed-meshheading:14990686-Animals,
pubmed-meshheading:14990686-Antibodies, Viral,
pubmed-meshheading:14990686-CD8-Positive T-Lymphocytes,
pubmed-meshheading:14990686-Genetic Vectors,
pubmed-meshheading:14990686-HIV Envelope Protein gp120,
pubmed-meshheading:14990686-Humans,
pubmed-meshheading:14990686-Mice,
pubmed-meshheading:14990686-Mice, Inbred BALB C,
pubmed-meshheading:14990686-Neutralization Tests,
pubmed-meshheading:14990686-Serotyping,
pubmed-meshheading:14990686-Viral Vaccines
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pubmed:year |
2004
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pubmed:articleTitle |
Neutralizing antibodies and CD8+ T lymphocytes both contribute to immunity to adenovirus serotype 5 vaccine vectors.
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pubmed:affiliation |
Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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