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PMID: 7684139 Published · ppublish English Journal Article Review

Molecular chaperones and the immune response.

Philosophical transactions of the Royal Society of London. Series B, Biological sciences ·Vol. 339 ·No. 1289 ·1993-03-29 ·Pages 363-7; discussion 367-8

Young D, Roman E, Moreno C, O'Brien R, Born W

Abstract

Molecular chaperones belonging to heat shock protein families have been identified as prominent antigens in the immune response to a wide variety of infections. Recognition of such highly conserved antigens may contribute to protective immunity but, in some circumstances, may also have pathological autoimmune consequences. Recognition of chaperones may be an inherent feature of the immune system. Peptide mapping experiments revealed an overlap between hsp 70-binding sites and immunodominant regions of three protein antigens, consistent with a possible functional activity for molecular chaperones in the processing and presentation of peptides during class II-restricted T lymphocyte responses. A functional role for molecular chaperones in antigen processing may be a factor which contributes to their immunogenicity.

MeSH Terms
Animals Antigens/immunology Binding Sites Chaperonins Epitopes/immunology Heat-Shock Proteins/metabolism Histocompatibility Antigens Class I/metabolism Histocompatibility Antigens Class II/metabolism Humans Proteins/metabolism T-Lymphocytes/immunology
Chemicals
Antigens Epitopes Heat-Shock Proteins Histocompatibility Antigens Class I Histocompatibility Antigens Class II Proteins Chaperonins
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Young D
MRC Tuberculosis and Related Infections Unit, Royal Postgraduate Medical School, Hammersmith Hospital, London, U.K.
Roman E
Moreno C
O'Brien R
Born W
Article Info
Journal
Philosophical transactions of the Royal Society of London. Series B, Biological sciences
Abbr.
Philos Trans R Soc Lond B Biol Sci
ISSN
0962-8436
Published
1993-03-29
Pages
363-7; discussion 367-8
Language
English
Region
England
NLM ID
7503623
Subset
IM
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