pubmed-article:11591771 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:11591771 | lifeskim:mentions | umls-concept:C1332717 | lld:lifeskim |
pubmed-article:11591771 | lifeskim:mentions | umls-concept:C1706438 | lld:lifeskim |
pubmed-article:11591771 | lifeskim:mentions | umls-concept:C0039194 | lld:lifeskim |
pubmed-article:11591771 | lifeskim:mentions | umls-concept:C0085358 | lld:lifeskim |
pubmed-article:11591771 | lifeskim:mentions | umls-concept:C0149678 | lld:lifeskim |
pubmed-article:11591771 | lifeskim:mentions | umls-concept:C1704632 | lld:lifeskim |
pubmed-article:11591771 | lifeskim:mentions | umls-concept:C0871261 | lld:lifeskim |
pubmed-article:11591771 | lifeskim:mentions | umls-concept:C0015219 | lld:lifeskim |
pubmed-article:11591771 | lifeskim:mentions | umls-concept:C1413244 | lld:lifeskim |
pubmed-article:11591771 | lifeskim:mentions | umls-concept:C2698600 | lld:lifeskim |
pubmed-article:11591771 | lifeskim:mentions | umls-concept:C2911692 | lld:lifeskim |
pubmed-article:11591771 | lifeskim:mentions | umls-concept:C1706817 | lld:lifeskim |
pubmed-article:11591771 | lifeskim:mentions | umls-concept:C0443199 | lld:lifeskim |
pubmed-article:11591771 | lifeskim:mentions | umls-concept:C0205360 | lld:lifeskim |
pubmed-article:11591771 | pubmed:issue | 8 | lld:pubmed |
pubmed-article:11591771 | pubmed:dateCreated | 2001-10-9 | lld:pubmed |
pubmed-article:11591771 | 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. | lld:pubmed |
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pubmed-article:11591771 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11591771 | pubmed:language | eng | lld:pubmed |
pubmed-article:11591771 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11591771 | pubmed:citationSubset | AIM | lld:pubmed |
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pubmed-article:11591771 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:11591771 | pubmed:month | Oct | lld:pubmed |
pubmed-article:11591771 | pubmed:issn | 0022-1767 | lld:pubmed |
pubmed-article:11591771 | pubmed:author | pubmed-author:SullivanJ LJL | lld:pubmed |
pubmed-article:11591771 | pubmed:author | pubmed-author:LuzuriagaKK | lld:pubmed |
pubmed-article:11591771 | pubmed:author | pubmed-author:LEES JSJ | lld:pubmed |
pubmed-article:11591771 | pubmed:author | pubmed-author:CatalinaM DMD | lld:pubmed |
pubmed-article:11591771 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:11591771 | pubmed:day | 15 | lld:pubmed |
pubmed-article:11591771 | pubmed:volume | 167 | lld:pubmed |
pubmed-article:11591771 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:11591771 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:11591771 | pubmed:pagination | 4450-7 | lld:pubmed |
pubmed-article:11591771 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
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pubmed-article:11591771 | pubmed:year | 2001 | lld:pubmed |
pubmed-article:11591771 | pubmed:articleTitle | Differential evolution and stability of epitope-specific CD8(+) T cell responses in EBV infection. | lld:pubmed |
pubmed-article:11591771 | pubmed:affiliation | Department of Pediatrics and Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA. | lld:pubmed |
pubmed-article:11591771 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:11591771 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:11591771 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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