CLONAL ANERGY BLOCKS THE RESPONSE TO IL-4, AS WELL AS THE PRODUCTION OF IL-2, IN DUAL-PRODUCING T-HELPER CELL CLONES

被引:0
|
作者
MUELLER, DL
CHIODETTI, L
BACON, PA
SCHWARTZ, RH
机构
[1] UNIV TEXAS,SW MED CTR,HAROLD C SIMMONS ARTHRITIS RES CTR,DALLAS,TX 75235
[2] NIAID,CELLULAR & MOLEC IMMUNOL LAB,BETHESDA,MD 20892
[3] NIAID,SW MED CTR,DEPT INTERNAL MED,BETHESDA,MD 20892
[4] UNIV BIRMINGHAM,DEPT RHEUMATOL,BIRMINGHAM B15 2TJ,W MIDLANDS,ENGLAND
来源
JOURNAL OF IMMUNOLOGY | 1991年 / 147卷 / 12期
关键词
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In this report we extend the in vitro clonal anergy model to examine the regulation of proliferation in T cells that secrete both IL-2 and IL-4. Newly cloned Ag-specific murine T cells are shown to depend on both IL-2 and IL-4 synthesis for maximal proliferation. Whereas IL-2 responsiveness is constitutive in these cells, IL-4 responsiveness develops only after Ag and APC stimulation. Remarkably, proliferation of these cells to Ag is sensitive to inhibition by clonal anergy, even though IL-4 synthesis remains inducible. Anergy in these cells is associated with an inability to respond to IL-4, in addition to the development of an IL-2 production defect. The results suggest that anergy induction may be capable of preventing the clonal expansion of autoreactive T cells producing both IL-2 and IL-4 in vivo.
引用
收藏
页码:4118 / 4125
页数:8
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