TOLERANCE INDUCTION BY CLONAL DELETION OF CD4+8+ THYMOCYTES INVITRO DOES NOT REQUIRE DEDICATED ANTIGEN-PRESENTING CELLS

被引:97
作者
PIRCHER, H
BRDUSCHA, K
STEINHOFF, U
KASAI, M
MIZUOCHI, T
ZINKERNAGEL, RM
HENGARTNER, H
KYEWSKI, B
MULLER, KP
机构
[1] TOKYO METROPOLITAN GERIATR HOSP & INST GERONTOL,DEPT PATHOL,TOKYO 173,JAPAN
[2] NATL INST HLTH,DEPT BLOOD PROD,TOKYO 141,JAPAN
[3] GERMAN CANC RES CTR,TUMOR IMMUNOL RES CTR,W-6900 HEIDELBERG 1,GERMANY
关键词
TOLERANCE; THYMOCYTES; TRANSGENIC MICE; NEGATIVE SELECTION; APOPTOSIS;
D O I
10.1002/eji.1830230315
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 cellular requirements of T-cell tolerance induction in the thymus by clonal deletion was investigated by using an in vitro assay: thymocytes from mice expressing a transgenic TcR specific for lymphocytic choriomeningitis virus (LCMV) and H-2D(b)) were co-cultured with various H-2b cell types as antigen-presenting cells in the presence of the antigenic LCMV peptide. The results revealed that all cell lines examined including embryonic and transformed fibroblasts. melanoma cells, cortical thymic epithelial cells. lymphomas and neuronal cells induced an antigen dose-dependent deletion of CD4+8+ thymocytes. Similarly, highly enriched accessory cell populations from thymus and spleen (macrophages, dendritic and cortical epithelial cells. i.e. thymic nurse cells) could induce antigen-specific depletion of immature CD4+8+ thymocytes. Depending on the cell type examined micromolar to picomolar concentration of LCMV peptide were required to induce deletion.The effectiveness of deletion by the different cell types did not correlate with their major histocompatibility class I expression level; it was, however, influenced by the presence of ICAM-1 adhesion molecules.
引用
收藏
页码:669 / 674
页数:6
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