Prevention of acute allograft rejection by antibody targeting of TIRC7, a novel T cell membrane protein

A novel 75 kDa membrane protein, TIRC7, is described that exhibits a central role in T cell activation in vitro and in vivo. Modulation of TIRC7-mediated signals with specific anti-TIRC7 antibodies in vitro efficiently prevents human T cell proliferation and IL-2 secretion. Moreover, anti-TIRC7 anti...

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Veröffentlicht in:Immunity (Cambridge, Mass.) Mass.), 1998-10, Vol.9 (4), p.509-518
Hauptverfasser: Utku, N, Heinemann, T, Tullius, S G, Bulwin, G C, Beinke, S, Blumberg, R S, Beato, F, Randall, J, Kojima, R, Busconi, L, Robertson, E S, Schülein, R, Volk, H D, Milford, E L, Gullans, S R
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Sprache:eng
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Zusammenfassung:A novel 75 kDa membrane protein, TIRC7, is described that exhibits a central role in T cell activation in vitro and in vivo. Modulation of TIRC7-mediated signals with specific anti-TIRC7 antibodies in vitro efficiently prevents human T cell proliferation and IL-2 secretion. Moreover, anti-TIRC7 antibodies specifically inhibit type 1 subset specific IFN-gamma expression but spare the type 2 cytokine IL-4. Diminished proliferation but not IFN-gamma secretion is reversible by exogenous rIL-2. An anti-TIRC7 antibody that cross-reacts with the 75 kDa rat homolog exhibits inhibition of rat alloimmune response in vitro and significantly prolongs kidney allograft survival in vivo. Targeting of TIRC7 may provide a novel therapeutic approach for modulation of the immune response.
ISSN:1074-7613
DOI:10.1016/s1074-7613(00)80634-2