Source:http://linkedlifedata.com/resource/pubmed/id/19950186
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2010-2-3
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pubmed:abstractText |
Measles continues to be an important cause of childhood mortality in developing countries. Measles virus (MV) is lymphotropic and infects high percentages of B- and T-lymphocytes in lymphoid tissues. Cellular immunity is considered crucial for viral clearance; however, MV-specific T-lymphocytes generated during primary infection also constitute a potential target for MV infection. We therefore aimed to identify T-lymphocyte subsets that can clear MV infection without becoming infected. To this end, we infected human EBV transformed B-lymphoblastic cell lines (B-LCL) with a recombinant MV strain expressing enhanced GFP, and co-cultured these with non-infected B-LCL resulting in rapid viral spread. MV-specific CD8(+) T-cell clones efficiently suppressed MV dissemination in autologous and HLA-matched, but not in HLA-mismatched B-LCL. In contrast, CD4(+) T-cell clones could not control MV dissemination but became a target for MV infection themselves. Furthermore, PBMC collected 6-9 months after acute measles and stimulated with autologous MV-infected B-LCL also efficiently suppressed MV dissemination; this was mediated by the fraction containing CD8(+) T-lymphocytes. In conclusion, we have developed a powerful tool to study cellular immunity against measles, and demonstrate that control of MV dissemination is mediated by virus-specific CD8(+) rather than by CD4(+) T-lymphocytes.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1521-4141
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
40
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
388-95
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pubmed:meshHeading |
pubmed-meshheading:19950186-B-Lymphocytes,
pubmed-meshheading:19950186-CD4-Positive T-Lymphocytes,
pubmed-meshheading:19950186-CD8-Positive T-Lymphocytes,
pubmed-meshheading:19950186-Cell Line, Transformed,
pubmed-meshheading:19950186-Cells, Cultured,
pubmed-meshheading:19950186-Coculture Techniques,
pubmed-meshheading:19950186-Cytotoxicity, Immunologic,
pubmed-meshheading:19950186-Flow Cytometry,
pubmed-meshheading:19950186-Green Fluorescent Proteins,
pubmed-meshheading:19950186-Humans,
pubmed-meshheading:19950186-Leukocytes, Mononuclear,
pubmed-meshheading:19950186-Measles virus,
pubmed-meshheading:19950186-Recombinant Fusion Proteins
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pubmed:year |
2010
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pubmed:articleTitle |
Specific CD8(+) T-lymphocytes control dissemination of measles virus.
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pubmed:affiliation |
Department of Virology, Erasmus MC, Rotterdam, The Netherlands.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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