Literature DB >> 11083810

Inhibition of T-cell response by Escherichia coli heat-labile enterotoxin-treated epithelial cells.

L M Lopes1, A Maroof, G Dougan, B M Chain.   

Abstract

Escherichia coli heat-labile enterotoxin (LT) is an extensively studied adjuvant of mucosal responses. Nevertheless, its mode of action as an adjuvant remains incompletely understood. In this study, we describe a simplified in vitro model with which to look at some aspects of immunoregulation by LT. The interaction of LT with the apical surface of a monolayer of CaCo-2 epithelial cells induces the release of a soluble factor which inhibits the antigen-induced release of interleukin-2 by T cells cultured at the basolateral side of the cells. The release of this factor requires the ADP-ribosylating activity of LT since the isolated B subunit, as well as an enzymatically silent LT mutant, loses biological activity in this model. The inhibitory activity is likely to be due to prostaglandin release, since it is blocked by indomethacin. The contribution of LT-induced prostaglandin release to the complex immunoregulatory activity of LT is discussed.

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Year:  2000        PMID: 11083810      PMCID: PMC97795          DOI: 10.1128/IAI.68.12.6891-6895.2000

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  19 in total

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Review 9.  Structure and mucosal adjuvanticity of cholera and Escherichia coli heat-labile enterotoxins.

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Journal:  Immunol Today       Date:  1999-11

10.  Cholera toxin suppresses interleukin (IL)-12 production and IL-12 receptor beta1 and beta2 chain expression.

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