CTLA-4 CAN FUNCTION AS A NEGATIVE REGULATOR OF T-CELL ACTIVATION

被引:1895
作者
WALUNAS, TL
LENSCHOW, DJ
BAKKER, CY
LINSLEY, PS
FREEMAN, GJ
GREEN, JM
THOMPSON, CB
BLUESTONE, JA
机构
[1] UNIV CHICAGO,DEPT MED,CHICAGO,IL 60637
[2] UNIV CHICAGO,HOWARD HUGHES MED INST,CHICAGO,IL 60637
[3] BRISTOL MYERS SQUIBB CO,PHARMACEUT RES INST,SEATTLE,WA 98121
[4] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,DEPT MED,DIV HEMATOL MALIGNANCIES,BOSTON,MA 02115
关键词
D O I
10.1016/1074-7613(94)90071-X
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
CD28 and CTLA-4 are related glycoproteins found on T cells. Ligation of CD28 following antigen receptor engagement provides a costimulatory signal required for T cell activation. Anti-CTLA-4 antibodies were generated to examine the role of the CTLA-4 receptor on murine T cells. Expression of CTLA-4 as a homodimer is up-regulated 2-3 days following T cell activation. Anti-CTLA-4 antibodies and Fab fragments augmented T cell proliferation in an allogeneic MLR. However, when optimal costimulation and Fc cross-linking were present, anti-CTLA-4 MAbs inhibited T cell proliferation. Together, these results suggest that the MAb may obstruct the interaction of CTLA-4 with its natural ligand and block a negative signal, or directly signal T cells to down-regulate immune function.
引用
收藏
页码:405 / 413
页数:9
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