T8 CELL REGULATION OF HUMAN B-CELL RESPONSIVENESS - REGULATORY INFLUENCES OF CD45RA+ AND CD45RA- T8 CELL SUBSETS

被引:11
|
作者
HIROHATA, S
机构
[1] Department of Medicine and Physical Therapy, University of Tokyo School of Medicine, Tokyo
关键词
D O I
10.1016/0008-8749(91)90176-C
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The immunoregulatory functions of human T8 cell subpopulations denned by mAb to the CD45RA molecule (2H4) were examined. Both CD45RA+ and CD45RA- T8 cells that had been treated with mitomycin C provided help for the production of immunoglobulins by B cells in cultures stimulated with immobilized mAb to CD3 (64.1). In contrast, both CD45RA+ and CD45RA- T8 cells that had not been treated with mitomycin C suppressed B cell responses in anti-CD3-stimulated cultures, although CD45RA+ T8 cells were more effective in this regard. Interleukin 2 (IL2) enhanced suppression by anti-CD3-activated CD45RA- T8 cells, whereas suppression by CD45RA+ T8 cells was almost maximal and not as much increased by IL2. The differentiation into suppressor-effector cells in this system appeared to involve the production of IL2, but not the production of Interferon (INF)-γ. Thus, CD45RA+ T8 cells produced higher amounts of IL2 but lower amounts of IFN-γ than CD45RA- T8 cells in anti-CD3-stimulated cultures. Moreover, addition of mAb to the p55 component of IL2 receptor (anti-Tac) inhibited the generation of suppressor activity from CD45RA+ and CD45RA- T8 cells. The pattern and magnitude of suppression of B cell responses by CD45RA+ and CD45RA- T4 cells were similar to that by CD45RA+ and CD45RA- T8 cells in this system. Finally, preactivated CD45RA+ T8 cells that had lost CD45RA expression suppressed the B cell responses as effectively as fresh CD45RA+ T8 cells. The results indicate that both CD45RA+ and CD45RA- T8 cells can help or suppress B cell responses. More importantly, the data suggest that the suppressor-effector function of human T cells may rather be related with the stages of the post-thymic differentiation as evidenced by the expression of the CD45RA molecule than represent the fully differentiated T cell subsets, such as T4 and T8 cells. In addition, the CD45RA molecule appeared not to be involved in the suppressor-effector function, but to determine the stage of post-thymic differentiation. © 1991.
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页码:15 / 26
页数:12
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