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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0026926,
umls-concept:C0039194,
umls-concept:C0330390,
umls-concept:C0439097,
umls-concept:C0524637,
umls-concept:C0542341,
umls-concept:C0871261,
umls-concept:C1327413,
umls-concept:C1332714,
umls-concept:C1511636,
umls-concept:C1547348,
umls-concept:C1552644,
umls-concept:C1704632,
umls-concept:C1705241,
umls-concept:C1705242,
umls-concept:C1706817,
umls-concept:C1823153,
umls-concept:C2003941,
umls-concept:C2348205,
umls-concept:C2349976,
umls-concept:C2911692
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pubmed:issue |
4
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pubmed:dateCreated |
1995-2-27
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pubmed:abstractText |
CD4+ and gamma delta T cells are activated readily by Mycobacterium tuberculosis. To examine their role in the human immune response to M. tuberculosis, CD4+ and gamma delta T cells from healthy tuberculin-positive donor were studied for patterns of Ag recognition, cytotoxicity, and cytokine production in response to M. tuberculosis-infected mononuclear phagocytes. Both T cell subsets responded to intact M. tuberculosis and its cytosolic Ags. However, CD4+ and gamma delta T cells differed in the range of cytosolic Ags recognized: reactivity to a wide m.w. range of Ags for CD4+ T cells, and a restricted pattern for gamma delta T cells, with dominance of Ags of 10 to 15 kDa. Both T cell subsets were equally cytotoxic for M. tuberculosis-infected monocytes. Furthermore, both CD4+ and gamma delta T cells produced large amounts of IFN-gamma: mean pg/ml of IFN-gamma in supernatants was 2458 +/- 213 for CD4+ and 2349 +/- 245 for gamma delta T cells. By filter-spot ELISA (ELISPOT), the frequency of IFN-gamma-secreting gamma delta T cells was one-half of that of CD4+ T cells in response to M. tuberculosis, suggesting that gamma delta T cells on a per cell basis were more efficient producers of IFN-gamma than CD4+ T cells. In contrast, CD4+ T cells produced more IL-2 than gamma delta T cells, which correlated with diminished T cell proliferation of gamma delta T cells compared with CD4+ T cells. These results indicate that CD4+ and gamma delta T cell subsets have similar effector functions (cytotoxicity, IFN-gamma production) in response to M. tuberculosis-infected macrophages, despite differences in the Ags recognized, IL-2 production, and efficiency of IFN-gamma production.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Bacterial,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-4,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, T-Cell...,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, T-Cell...
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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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 |
154
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1786-96
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:7836763-Antigens, Bacterial,
pubmed-meshheading:7836763-CD4-Positive T-Lymphocytes,
pubmed-meshheading:7836763-Cells, Cultured,
pubmed-meshheading:7836763-Cytotoxicity, Immunologic,
pubmed-meshheading:7836763-Humans,
pubmed-meshheading:7836763-Interferon-gamma,
pubmed-meshheading:7836763-Interleukin-2,
pubmed-meshheading:7836763-Interleukin-4,
pubmed-meshheading:7836763-Mycobacterium tuberculosis,
pubmed-meshheading:7836763-Receptors, Antigen, T-Cell, alpha-beta,
pubmed-meshheading:7836763-Receptors, Antigen, T-Cell, gamma-delta,
pubmed-meshheading:7836763-Tuberculosis
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pubmed:year |
1995
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pubmed:articleTitle |
CD4+ alpha beta T cell and gamma delta T cell responses to Mycobacterium tuberculosis. Similarities and differences in Ag recognition, cytotoxic effector function, and cytokine production.
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pubmed:affiliation |
Department of Medicine, Case Western Reserve University, Cleveland, Ohio.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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