Source:http://linkedlifedata.com/resource/pubmed/id/11591771
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rdf:type | |
lifeskim:mentions |
umls-concept:C0015219,
umls-concept:C0039194,
umls-concept:C0085358,
umls-concept:C0149678,
umls-concept:C0205360,
umls-concept:C0443199,
umls-concept:C0871261,
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 |
2001-10-9
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pubmed:abstractText |
Murine models of lymphocytic choriomeningitis virus infection suggest that the memory CD8(+) T cell repertoire is reflective of the CD8(+) T cell repertoire generated during acute infection. Less is known regarding the evolution of CD8(+) T cell repertoires during human viral infections. We therefore examined epitope-specific CD8(+) T cell responses in a large cohort of individuals with acute through latent Epstein-Barr virus infection. Using 16 of 20 published EBV epitopes restricted by HLA-A2, HLA-A3 or HLA-B7, we showed that lytic cycle-specific CD8(+) T cell responses predominated during acute EBV infection. However, whereas HLA-A2(+)-restricted BMLF-1-specific CD8(+) T cell responses were maintained through latency, HLA-A2(+)- and HLA-B7(+)-restricted BZLF-1, as well as HLA-A3(+)-restricted BRLF-1 CD8(+) T cell responses, were generated but not readily maintained. Analyses of CD8(+) T cell responses to EBV latent cycle Ags showed delayed detection and lower frequencies of latent epitope-specific CD8(+) T cell responses during acute EBV infection, with maintenance of these responses 1 yr post-EBV infection. Early BMLF-1 and EBNA-3A epitope-specific CD8(+) T cell frequencies did not correlate with their frequencies at 1 yr postinfection. Interestingly, populations of EBV-specific CD8(+) T cells were stable during 20 mo in our long term EBV-seropositive populations, suggesting homeostasis between virus and the host immune system. This study demonstrates that CD8(+) T cell repertoires generated during persistent viral infections are not simply reflective of the initial pool of CD8(+) T cells and provides evidence that the generation of CD8(+) T cell responses to a persistent infection is a dynamic process.
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pubmed:grant | |
pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Epitopes,
http://linkedlifedata.com/resource/pubmed/chemical/Epstein-Barr Virus Nuclear Antigens,
http://linkedlifedata.com/resource/pubmed/chemical/HLA-A Antigens,
http://linkedlifedata.com/resource/pubmed/chemical/HLA-B Antigens,
http://linkedlifedata.com/resource/pubmed/chemical/Oligopeptides,
http://linkedlifedata.com/resource/pubmed/chemical/Viral Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
167
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4450-7
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:11591771-Acute Disease,
pubmed-meshheading:11591771-Adolescent,
pubmed-meshheading:11591771-Adult,
pubmed-meshheading:11591771-CD8-Positive T-Lymphocytes,
pubmed-meshheading:11591771-Cohort Studies,
pubmed-meshheading:11591771-Epitopes,
pubmed-meshheading:11591771-Epstein-Barr Virus Infections,
pubmed-meshheading:11591771-Epstein-Barr Virus Nuclear Antigens,
pubmed-meshheading:11591771-HLA-A Antigens,
pubmed-meshheading:11591771-HLA-B Antigens,
pubmed-meshheading:11591771-Herpesvirus 4, Human,
pubmed-meshheading:11591771-Humans,
pubmed-meshheading:11591771-Immunologic Memory,
pubmed-meshheading:11591771-Oligopeptides,
pubmed-meshheading:11591771-Viral Proteins,
pubmed-meshheading:11591771-Virus Latency
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pubmed:year |
2001
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pubmed:articleTitle |
Differential evolution and stability of epitope-specific CD8(+) T cell responses in EBV infection.
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pubmed:affiliation |
Department of Pediatrics and Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01605, 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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