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

被引:67
作者
Utku, N
Heinemann, T
Tullius, SG
Bulwin, GC
Beinke, S
Blumberg, RS
Beato, F
Randall, J
Kojima, R
Busconi, L
Robertson, ES
Schülein, R
Volk, HD
Milford, EL
Gullans, SR
机构
[1] Humboldt Univ, Charite, Inst Med Immunol, D-10098 Berlin, Germany
[2] Humboldt Univ, Charite, Chirurg Klin, D-10098 Berlin, Germany
[3] Univ Bonn, Kekule Inst Organ Chem & Biochem, D-53121 Bonn, Germany
[4] Forschungsinst Mol Pharmakol, D-10315 Berlin, Germany
[5] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[6] Harvard Inst Med, Boston, MA 02115 USA
关键词
D O I
10.1016/S1074-7613(00)80634-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 lFN-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.
引用
收藏
页码:509 / 518
页数:10
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