Activation of murine T cells by bacterial superantigens requires B7-mediated costimulation.

Abstract:

:Staphylococcus enterotoxins bind class II MHC molecules on antigen-presenting cells (APC) and stimulate T cells expressing appropriate V beta gene products. Although the role of non-TcR-associated costimulatory receptors during antigen-specific T cell stimulation has been clearly established, the involvement of costimulatory activity in T cell activation by superantigens (SAgs) has been the matter of controversy. The aim of this study was to evaluate the role of the costimulatory-receptor ligand molecules CD28/B7 on bacterial SAg-mediated activation of naive murine T cells. We demonstrate in this report that a combination of monoclonal antibodies to murine B7.1 and B7.2 molecules inhibits the in vitro response of naive T cells to SAgs SEA, SEB, and TSST-1. The inhibition of T cell responses required simultaneous blocking of B7.1 and B7.2, suggesting that either B7.1 or B7.2 is sufficient to provide costimulatory signals to naive T cells in response to bacterial exotoxins. Inhibition of T cell activation by antibodies to B7-related molecules can be overcome by antibodies to CD28, a finding in agreement with the hypothesis that CD28-mediated signals participate in T cell activation by bacterial SAgs. These observations suggest that, as demonstrated for conventional antigen, T cell activation by SAgs requires the coordinated participation of TcR- and CD28-derived signals.

journal_name

Cell Immunol

journal_title

Cellular immunology

authors

Muraille E,De Smedt T,Thielemans K,Urbain J,Moser M,Leo O

doi

10.1006/cimm.1995.1084

subject

Has Abstract

pub_date

1995-05-01 00:00:00

pages

315-20

issue

2

eissn

0008-8749

issn

1090-2163

pii

S0008-8749(85)71084-2

journal_volume

162

pub_type

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