Functional heterogeneity of L3T4+ T cells in MRL-lpr/lpr mice. L3T4+ T cells suppress major histocompatibility complex-self-restricted L3T4+ T helper cell function in association with autoimmunity.
Functional heterogeneity of L3T4+ T cells in MRL-lpr/lpr mice. L3T4+ T cells suppress major histocompatibility complex-self-restricted L3T4+ T helper cell function in association with autoimmunity.
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MRL-LPR/LPR小鼠L3T4+ T细胞的功能异质性。 L3T4+ T细胞抑制了主要的组织相容性复合物限制的L3T4+ T辅助细胞功能与自身免疫相关。
DOI:
10.1084/jem.168.6.2165
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发表时间:
1988-12-01
影响因子:
15.3
通讯作者:
SHEARER, GM
中科院分区:
文献类型:
--
作者:
VIA, CS;SHEARER, GM
The present study demonstrates in MRl-lpr/lpr autoimmune mice an age- dependent loss of MHC-self-restricted function by L3T4+ Th. This defect is not present in age-matched, congenic MRL-+/+ spleen cells and appears to be due to the presence of suppressor cells that are selective for L3T4+ Th and not for Lyt-2+ Th. Surprisingly, the suppressor cells are also L3T4+ T cells and can suppress the IL-2 production of congenic MRL/+ L3T4+ Th to MHC-self-restricted antigens. These data support the idea of functional specialization within the L3T4+ population of T cells. Because L3T4+ suppressor cells are detected late in the course of autoimmunity, we interpret their presence not as a primary initiating event in the development of autoimmunity, but rather as a compensatory mechanism. Additionally, similar suppression of L3T4+ Th function has also been reported in a murine graft-vs.-host model of autoimmunity, suggesting that the suppressor cells represent an immunoregulatory mechanism that is a common feature of autoimmunity. Since excessive class II-restricted Th activity for B cells has been reported for both models of autoimmunity, L3T4+ suppressor cells may represent an attempt to down regulate such excessive Th activity. These findings may be relevant to human autoimmune diseases, such as systemic lupus erythematosus, in which B cell hyperactivity is also associated with reduced IL-2 production by Th.
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影响因子:
64.8
作者:
LIEW, FY
通讯作者:
LIEW, FY
影响因子:
5.4
作者:
PFIZENMAIER, K;SCHEURICH, P;WAGNER, H
通讯作者:
WAGNER, H
DOI:
10.1084/jem.157.2.730
发表时间:
1983-02-01
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Prud'Homme GJ;Park CL;Fieser TM;Kofler R;Dixon FJ;Theofilopoulos AN
通讯作者:
Theofilopoulos AN
影响因子:
15.3
作者:
Altman, A;Theofilopoulos, A N;Weiner, R;Katz, D H;Dixon, F J
通讯作者:
Dixon, F J
影响因子:
8.7
作者:
CANTOR, H;BOYSE, EA
通讯作者:
BOYSE, EA