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PMID: 2117633 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

HLA-DR alleles differ in their ability to present staphylococcal enterotoxins to T cells.

The Journal of experimental medicine ·Vol. 172 ·No. 3 ·1990-09-01 ·Pages 709-17

Herman A, Croteau G, Sekaly RP, Kappler J, Marrack P

Abstract

Staphylococcal enterotoxins (SEs) have been shown to bind to major histocompatibility complex (MHC) class II proteins and stimulate T cells in a V beta-specific manner, and these V beta specificities for various SEs have been well documented in mice and humans. This study was undertaken in order to examine the ability of human class II molecules to present SEs to human and murine T cell hybridomas. Using a panel of transfectants expressing individual HLA class II antigens, we have shown that HLA-DR alleles differ in their ability to bind and present SEs. Since the HLA-DR proteins share a common alpha chain, these results indicate that the polymorphic beta chain plays an important role in SE binding and presentation to T cells. In addition, we have shown that human class II isotypes markedly differ in their ability to present SEs. The results of this study should provide information on the region of MHC class II molecules that interacts with foreign, and perhaps self, super-antigens.

MeSH Terms
Alleles Animals Cell Line Enterotoxins/immunology Genes, MHC Class II HLA-DR Antigens/genetics,immunology Histocompatibility Antigens Class II/genetics,immunology Humans Mice Staphylococcus/immunology T-Lymphocytes/immunology Transfection
Chemicals
Enterotoxins HLA-DR Antigens Histocompatibility Antigens Class II
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Herman A
Howard Hughes Medical Institute, Department of Medicine, National Jewish Center for Immunology and Respiratory Medicine, Denver, Colorado 80206.
Croteau G
Sekaly R P
Kappler J
Marrack P
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1990-09-01
Pages
709-17
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2188560
Subset
IM
Grants
NIAID NIH HHS · AI-17134 · United States
NIAID NIH HHS · AI-18785 · United States
NIAID NIH HHS · AI-22259 · United States
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