Identification of a costimulatory molecule rapidly induced by CD40L as CD44H

被引:107
作者
Guo, Y
Wu, Y
Shinde, S
Sy, MS
Aruffo, A
Liu, Y
机构
[1] NYU, MED CTR, DEPT PATHOL, MICHAEL HEIDELBERGER DIV IMMUNOL, NEW YORK, NY 10016 USA
[2] NYU, MED CTR, KAPLAN COMPREHENS CANC CTR, NEW YORK, NY 10016 USA
[3] CASE WESTERN RESERVE UNIV, CTR CANC RES, CLEVELAND, OH 44106 USA
[4] CASE WESTERN RESERVE UNIV, DEPT DERMATOL, CLEVELAND, OH 44106 USA
[5] CASE WESTERN RESERVE UNIV, DEPT DERMATOL, INST PATHOL, CLEVELAND, OH 44106 USA
[6] CASE WESTERN RESERVE UNIV, CTR CANC RES, CLEVELAND, OH 44106 USA
[7] BRISTOL MYERS SQUIBB PHARMACEUT RES INST, SEATTLE, WA 98121 USA
关键词
D O I
10.1084/jem.184.3.955
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The interaction between CD40 ligand and CD40 is critical for activation of T and B cells in vivo. We have recently demonstrated that this interaction rapidly induces a novel costimulatory activity distinct from B7 and independent of CD28. To study the molecular basis of the costimulatory activity, we have produced a novel monoclonal antibody, TM-1, that binds an 85-kilodalton costimulatory molecule rapidly induced by CD40L. Expression cloning reveals that TM-1 binds CD44H. CD44H expressed on Chinese hamster ovary cells has potent costimulatory activity for clonal expansion of T cells isolated from both wild-type mice and those with a targeted mutation of CD28. Thus, CD44H costimulates T cell proliferation by a CD28-independent mechanism. These results revealed that CD44H is a costimulatory molecule rapidly induced by CD40L.
引用
收藏
页码:955 / 961
页数:7
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