Literature DB >> 1936123

Temperature-induced stress abrogates co-stimulatory function in antigen-presenting cells.

G Kuperberg1, J Ellis, J Marcinkiewicz, B M Chain.   

Abstract

This study examines the effect of heat-induced stress on the function of splenic antigen-presenting cells. Heat shock (at 41 degrees C, 45 degrees C) profoundly inhibits the ability of this population to stimulate antigen-specific proliferation in ex vivo, or short-term cultures of T cells. This inhibition is not due to the release of suppressor factors from the antigen-presenting cells, nor to a lack of interleukin 1. Comparison of the effect of heat shock on presentation to a T cell hybridoma suggest that heat shock may affect the ability of antigen-presenting cells to deliver a co-stimulatory signal to the T cell. The implication of these findings in terms of the regulation of autoimmune phenomena is discussed.

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Year:  1991        PMID: 1936123     DOI: 10.1002/eji.1830211121

Source DB:  PubMed          Journal:  Eur J Immunol        ISSN: 0014-2980            Impact factor:   5.532


  2 in total

1.  Heat-stressed CD4+ T lymphocytes: differential modulations of adhesiveness to extracellular matrix glycoproteins, proliferative responses and tumour necrosis factor-alpha secretion.

Authors:  R Hershkoviz; R Alon; Y A Mekori; D Gilat; L Cahalon; A Miller; O Lider
Journal:  Immunology       Date:  1993-06       Impact factor: 7.397

2.  Heat shock protein 70 overexpression affects the response to ultraviolet light in murine fibroblasts. Evidence for increased cell viability and suppression of cytokine release.

Authors:  M M Simon; A Reikerstorfer; A Schwarz; C Krone; T A Luger; M Jäättelä; T Schwarz
Journal:  J Clin Invest       Date:  1995-03       Impact factor: 14.808

  2 in total

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