pubmed-article:12021347 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:12021347 | lifeskim:mentions | umls-concept:C0042216 | lld:lifeskim |
pubmed-article:12021347 | lifeskim:mentions | umls-concept:C0522424 | lld:lifeskim |
pubmed-article:12021347 | lifeskim:mentions | umls-concept:C0035820 | lld:lifeskim |
pubmed-article:12021347 | lifeskim:mentions | umls-concept:C0012854 | lld:lifeskim |
pubmed-article:12021347 | lifeskim:mentions | umls-concept:C0042210 | lld:lifeskim |
pubmed-article:12021347 | lifeskim:mentions | umls-concept:C0805586 | lld:lifeskim |
pubmed-article:12021347 | lifeskim:mentions | umls-concept:C2587213 | lld:lifeskim |
pubmed-article:12021347 | lifeskim:mentions | umls-concept:C0205349 | lld:lifeskim |
pubmed-article:12021347 | lifeskim:mentions | umls-concept:C1511545 | lld:lifeskim |
pubmed-article:12021347 | pubmed:issue | 12 | lld:pubmed |
pubmed-article:12021347 | pubmed:dateCreated | 2002-5-21 | lld:pubmed |
pubmed-article:12021347 | pubmed:abstractText | Cellular immune responses against epitopes in conserved Gag and Pol sequences of human immunodeficiency virus type 1 have become popular targets for candidate AIDS vaccines. Recently, we used a simian-human immunodeficiency virus model (SHIV 89.6P) with macaques to demonstrate the control of a pathogenic mucosal challenge by priming with Gag-Pol-Env-expressing DNA and boosting with Gag-Pol-Env-expressing recombinant modified vaccinia virus Ankara (rMVA). Here we tested Gag-Pol DNA priming and Gag-Pol rMVA boosting to evaluate the contribution of anti-Env immune responses to viral control. The Gag-Pol vaccine raised frequencies of Gag-specific T cells similar to those raised by the Gag-Pol-Env vaccine. Following challenge, these rapidly expanded to counter the challenge infection. Despite this, the control of the SHIV 89.6P challenge was delayed and inconsistent in the Gag-Pol-vaccinated group and all of the animals underwent severe and, in most cases, sustained loss of CD4(+) cells. Interestingly, most of the CD4(+) cells that were lost in the Gag-Pol-vaccinated group were uninfected cells. We suggest that the rapid appearance of binding antibody for Env in Gag-Pol-Env-vaccinated animals helped protect uninfected CD4(+) cells from Env-induced apoptosis. Our results highlight the importance of immune responses to Env, as well as to Gag-Pol, in the control of immunodeficiency virus challenges and the protection of CD4(+) cells. | lld:pubmed |
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pubmed-article:12021347 | pubmed:language | eng | lld:pubmed |
pubmed-article:12021347 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12021347 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:12021347 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:12021347 | pubmed:month | Jun | lld:pubmed |
pubmed-article:12021347 | pubmed:issn | 0022-538X | lld:pubmed |
pubmed-article:12021347 | pubmed:author | pubmed-author:KlosIu SIuS | lld:pubmed |
pubmed-article:12021347 | pubmed:author | pubmed-author:McClureHarold... | lld:pubmed |
pubmed-article:12021347 | pubmed:author | pubmed-author:MontefioriDav... | lld:pubmed |
pubmed-article:12021347 | pubmed:author | pubmed-author:MossBernardB | lld:pubmed |
pubmed-article:12021347 | pubmed:author | pubmed-author:AltmanJohn... | lld:pubmed |
pubmed-article:12021347 | pubmed:author | pubmed-author:VillingerFran... | lld:pubmed |
pubmed-article:12021347 | pubmed:author | pubmed-author:StapransSilvi... | lld:pubmed |
pubmed-article:12021347 | pubmed:author | pubmed-author:SmithJames... | lld:pubmed |
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pubmed-article:12021347 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:12021347 | pubmed:volume | 76 | lld:pubmed |
pubmed-article:12021347 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:12021347 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:12021347 | pubmed:pagination | 6138-46 | lld:pubmed |
pubmed-article:12021347 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:12021347 | pubmed:year | 2002 | lld:pubmed |
pubmed-article:12021347 | pubmed:articleTitle | Critical role for Env as well as Gag-Pol in control of a simian-human immunodeficiency virus 89.6P challenge by a DNA prime/recombinant modified vaccinia virus Ankara vaccine. | lld:pubmed |
pubmed-article:12021347 | pubmed:affiliation | Vaccine Research Center, Emory University School of Medicine, Atlanta, Georgia 30322, USA. | lld:pubmed |
pubmed-article:12021347 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:12021347 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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