DIFFERENCES IN RESPONSIVENESS TO CD3 STIMULATION BETWEEN NAIVE AND MEMORY CD4+ T-CELLS CANNOT BE OVERCOME BY CD28 COSTIMULATION

被引:35
|
作者
KUIPER, H
BROUWER, M
DEBOER, M
PARREN, P
VANLIER, RAW
机构
[1] NETHERLANDS RED CROSS,BLOOD TRANSFUS SERV,CENT LAB,DEPT CLIN VIROIMMUNOL,1066 CX AMSTERDAM,NETHERLANDS
[2] UNIV AMSTERDAM,EXPTL & CLIN IMMUNOL LAB,AMSTERDAM,NETHERLANDS
[3] INNOGENET,GHENT,BELGIUM
关键词
CD28; B7; CD4(+)CD45RA(+) CELLS; CD4(+)CD45RO(+) CELLS; T CELL ACTIVATION;
D O I
10.1002/eji.1830240903
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Activation of naive CD4(+) T cells is essential for the induction of primary immune responses. However, this subset is less responsive to signaling via T cell receptor/CD3 (TcR/CD3) complex than memory CD4(+) cells. For mitogenic activation of T cells, in addition to triggering of the TcR/CD3 complex, costimulatory signals are required that can be generated by surface structures present on the antigen-presenting cells. We investigated here whether differences in responsiveness to TcR/CD3 stimulation of naive and memory cells can be overcome by the costimulatory pathway B7/CD28. Using a B7-dependent system we show that even in the presence of optimal CD28 costimulation, CD4(+) naive cells still have more stringent TcR/CD3 activation requirements than memory cells. Furthermore, titration of the B7 signal revealed that for activation of naive CD4(+) cells a higher level of cross-linking of CD28 molecules is required than for memory cells. Thus, our results show that at least two signals are required for activation of both CD4(+) memory and naive cells, but that for activation of naive cells higher cross-linking of both CD3 and CD28 molecules is necessary.
引用
收藏
页码:1956 / 1960
页数:5
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