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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1996-10-23
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pubmed:abstractText |
We have isolated two subtypes of helper T cells from human tonsils: CD4+CD57+ cells, mostly located in the germinal center (GC), and CD4+CD57- cells, distributed through the interfollicular areas but also present in the GC. In a functional study, we have compared the capacities of these T-cell subtypes to stimulate B cells in cocultures. In order to block T-cell proliferation while maintaining their activation level, we pretreated isolated T cells with mitomycin C prior to culture in the presence of B cells and added polyclonal activators such as PHA and Con A, combined or not with IL-2. Contrary to CD4+ CD57- cells, CD4+CD57+ cells did not markedly enhance B-cell proliferation. Even when sIgD.B cells typical of germinal center cells were tested, the CD4+CD57+ cells had no significant effect. This is in accordance with the location of these cells: They mainly occupy the light zones of the GC where few B cells divide. Even when added to preactivated, actively proliferating cells, CD4+CD57 cells failed to modulate B-cell multiplication. On the supernatants of B-cell-T-cell cocultures, we examined by the ELISA technique the effect of T cells on Ig synthesis. Contrary to CD57+ T cells, whose effect was strong, CD57- T cells weakly stimulated Ig synthesis. More IgM than IgG was generally found. Because CD57 antigen is a typical marker of natural killer cells, we tested the cytolytic activity of tonsillar CD4+CD57+ cells on K562 target cells. Unlike NK cells, neither CD4+CD57+ nor CD4+CD57- cells exhibit any cytotoxicity. Thus, germinal center CD4+CD57+ cells are not cytolytic and do not strongly stimulate either B-cell proliferation or Ig secretion. CD4+CD57- cells, however, enhance B-cell proliferation and differentiation, thus acting like the classical helper cells of the T-dependent areas.
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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:issn |
1044-6672
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
4
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
189-97
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:8770558-Antigens, CD4,
pubmed-meshheading:8770558-Antigens, CD57,
pubmed-meshheading:8770558-B-Lymphocytes,
pubmed-meshheading:8770558-CD4-Positive T-Lymphocytes,
pubmed-meshheading:8770558-Cytotoxicity, Immunologic,
pubmed-meshheading:8770558-Humans,
pubmed-meshheading:8770558-Immunoglobulins,
pubmed-meshheading:8770558-Lymphocyte Activation,
pubmed-meshheading:8770558-Lymphocyte Cooperation,
pubmed-meshheading:8770558-Palatine Tonsil,
pubmed-meshheading:8770558-T-Lymphocyte Subsets,
pubmed-meshheading:8770558-T-Lymphocytes, Helper-Inducer,
pubmed-meshheading:8770558-Tumor Cells, Cultured
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pubmed:year |
1995
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pubmed:articleTitle |
Human germinal center CD4+CD57+ T cells act differently on B cells than do classical T-helper cells.
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pubmed:affiliation |
Institute of Human Histology, University of Liège, Belgium.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
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