UNCOVERING OF FUNCTIONAL ALTERNATIVE CTLA-4 COUNTER-RECEPTOR IN B7-DEFICIENT MICE

被引:395
作者
FREEMAN, GJ
BORRIELLO, F
HODES, RJ
REISER, H
HATHCOCK, KS
LASZLO, G
MCKNIGHT, AJ
KIM, J
DU, LN
LOMBARD, DB
GRAY, GS
NADLER, LM
SHARPE, AH
机构
[1] BRIGHAM & WOMENS HOSP,DEPT PATHOL,IMMUNOL RES DIV,BOSTON,MA 02115
[2] REPLIGEN CORP,CAMBRIDGE,MA 02139
[3] HARVARD UNIV,SCH MED,DEPT MED,BOSTON,MA 02115
[4] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,DIV HEMATOL MALIGNANCIES,BOSTON,MA 02115
[5] NCI,EXPTL IMMUNOL BRANCH,BETHESDA,MD 20892
[6] NIA,BETHESDA,MD 20892
[7] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,DIV LYMPHOCYTE BIOL,BOSTON,MA 02115
[8] HARVARD UNIV,SCH MED,DEPT PATHOL,BOSTON,MA 02115
关键词
D O I
10.1126/science.7694362
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
B7 delivers a costimulatory signal through CD28, resulting in interleukin-2 secretion and T cell proliferation. Blockade of this pathway results in T cell anergy. The in vivo role of B7 was evaluated with B7-deficient mice. These mice had a 70 percent decrease in costimulation of the response to alloantigen. Despite lacking B7 expression, activated B cells from these mice bound CTLA-4 and GL1 monoclonal antibody, demonstrating that alternative CTLA-4 ligand or ligands exist. These receptors are functionally important because the residual allogenic mixed lymphocyte responses were blocked by CTLA4Ig. Characterization of these CTLA-4 ligands should lead to strategies for manipulating the immune response.
引用
收藏
页码:907 / 909
页数:3
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