INTERACTIONS BETWEEN STAPHYLOCOCCAL SUPERANTIGENS AND HUMAN T-CELL CLONES ARE PREDOMINANTLY BUT NOT EXCLUSIVELY GOVERNED BY THEIR T-CELL RECEPTOR V-BETA USAGE

Citation
Kea. Lundin et al., INTERACTIONS BETWEEN STAPHYLOCOCCAL SUPERANTIGENS AND HUMAN T-CELL CLONES ARE PREDOMINANTLY BUT NOT EXCLUSIVELY GOVERNED BY THEIR T-CELL RECEPTOR V-BETA USAGE, Scandinavian journal of immunology, 39(4), 1994, pp. 387-394
Citations number
39
Categorie Soggetti
Immunology
ISSN journal
03009475
Volume
39
Issue
4
Year of publication
1994
Pages
387 - 394
Database
ISI
SICI code
0300-9475(1994)39:4<387:IBSSAH>2.0.ZU;2-3
Abstract
Staphylococcal exotoxins (SE) are potent mitogens for human and murine T cells. Extensive studies in mice have demonstrated strict correlati ons between T-cell responses to individual SE and TCR V beta expressio n. Studies examining the TCR V beta expression of SE-activated human p eripheral blood T cells also suggest close correlations, whereas the d ata reported using human T-cell clones (TCC) are conflicting. We have determined the cDNA TCRB sequences of 52 different human TCC, expressi ng 35 different T-cell receptor V beta (TCRBV)-encoded sequences. The TCC were tested in proliferative assays using nine different SE. Most of these TCC express V beta s which have not been tested previously in studies examining interaction between TCC and SE. The SE stimulated a variable fraction (1/48-31/52) of the TCC. The ability of a given SE to stimulate TCC in many cases correlated with V beta expression, but several exceptions were found. With one possible exception, comparison s between deduced amino-acid sequences within the 'fourth hypervariabl e region' of the TCR beta chain and SE responsiveness did not reveal p otential SE binding motifs. We conclude that the reactivity of T cells towards SE is governed mainly by their TCR V beta expression. However , the authors' results also suggest that the interaction between SE an d human T cells may involve elements unidentified as yet which are in addition to the beta chain of the TCR.