Source:http://linkedlifedata.com/resource/pubmed/id/16910834
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rdf:type | |
lifeskim:mentions |
umls-concept:C0004083,
umls-concept:C0007584,
umls-concept:C0008115,
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umls-concept:C0021311,
umls-concept:C0039194,
umls-concept:C0085358,
umls-concept:C0332307,
umls-concept:C0449560,
umls-concept:C0456603,
umls-concept:C0871261,
umls-concept:C1332714,
umls-concept:C1332717,
umls-concept:C1413244,
umls-concept:C1704632,
umls-concept:C1706438,
umls-concept:C1706817,
umls-concept:C2698600,
umls-concept:C2911692
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pubmed:issue |
8
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pubmed:dateCreated |
2006-8-16
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pubmed:abstractText |
CD4+ T cell counts and CD4+:CD8+ T cell ratios represent key determinants of HIV disease progression and infectivity. However, the relationship between the HIV-1-specific cytotoxic T lymphocyte (CTL) response and these determinants has not been elucidated for all HIV-1B and HIV-1C proteins. In the present study, virusspecific T cell responses to HIV-1B and HIV-1C proteins were analyzed with interferon gamma (IFN-gamma) enzyme- linked immunospot (ELISpot) assays using synthetic overlapping peptides corresponding to naturally occurring HIV-1B and HIV-1C consensus sequences. For Gag/Gag p24/Gag p17, a correlation between T cell responses and CD4+ T cell count in HIV-1 clade B and clade C was seen: elevated T cell response resulted in higher CD4+ T cell production. A statistically significant correlation between the Pol-specific T cell response and CD4+ T cell counts was also found in HIV-1 subtype C. For all HIV-1B and HIV-1C proteins, a correlation between the HIV-1-specific T cell response and CD4+:CD8+ T cell ratios was found for Tat and Pol proteins. CD4+ T cell counts in patients with Tat and/or Rev T cell response were higher than in patients without Tat and/or Rev T cell response. We suggest that this correlation within HIV-1B and HIV-1C Gag p24/Gag p17 responses makes the Gag p24/Gag p17 region a potential vaccine candidate and that HIV-1-specific CTL epitopes toward Pol are important in controlling HIV-1 infection; we emphasize that future vaccination strategies should include these early antigens, Tat and Rev.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Gene Products, gag,
http://linkedlifedata.com/resource/pubmed/chemical/HIV Antigens,
http://linkedlifedata.com/resource/pubmed/chemical/HIV Core Protein p24,
http://linkedlifedata.com/resource/pubmed/chemical/Viral Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/gag Gene Products, Human...,
http://linkedlifedata.com/resource/pubmed/chemical/p17 protein, Human...
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0889-2229
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
22
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
780-7
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:16910834-Adolescent,
pubmed-meshheading:16910834-Adult,
pubmed-meshheading:16910834-CD4 Lymphocyte Count,
pubmed-meshheading:16910834-CD4-CD8 Ratio,
pubmed-meshheading:16910834-China,
pubmed-meshheading:16910834-Female,
pubmed-meshheading:16910834-Gene Products, gag,
pubmed-meshheading:16910834-HIV Antigens,
pubmed-meshheading:16910834-HIV Core Protein p24,
pubmed-meshheading:16910834-HIV Infections,
pubmed-meshheading:16910834-HIV-1,
pubmed-meshheading:16910834-Humans,
pubmed-meshheading:16910834-Male,
pubmed-meshheading:16910834-Middle Aged,
pubmed-meshheading:16910834-Species Specificity,
pubmed-meshheading:16910834-T-Lymphocytes, Cytotoxic,
pubmed-meshheading:16910834-Viral Load,
pubmed-meshheading:16910834-Viral Proteins,
pubmed-meshheading:16910834-gag Gene Products, Human Immunodeficiency Virus
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pubmed:year |
2006
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pubmed:articleTitle |
Association between HIV Type 1-specific T cell responses and CD4+ T cell counts or CD4+:CD8+ T cell ratios in HIV Type 1 subtype B infection in China.
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pubmed:affiliation |
Department of Infectious Diseases, Tangdu Hospital Affiliated to the Fourth Military Medical University, Xi'an 710038, Peoples Republic of China.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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