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由于主要组织相容性复合体I类和II类差异而发生移植物抗宿主反应的小鼠中巨噬细胞的免疫抑制活性。

Immunosuppressive activity of macrophages in mice undergoing graft-versus-host reaction due to major histocompatibility complex class I plus II difference.

作者信息

Ikarashi Y, Kawai K, Watanabe H, Matsumoto Y, Omata S, Fujiwara M

机构信息

Department of Biosystem Science, Graduate School of Science and Technology, Niigata University, Japan.

出版信息

Immunology. 1993 May;79(1):95-102.

Abstract

In a previous report, we showed that the injection of parental CD4+ T cells into major histocompatibility complex (MHC) class II disparate F1 hybrid mice induces autoimmune-like graft versus-host reaction (GVHR) resembling systemic lupus erythematosus (SLE) and the hepatic lesion of primary biliary cirrhosis (PBC). In the present study, we examined whether or not simultaneous or subsequent injection of CD8+ T cells changes the GVHR form. When parental CD8+ T cells together with CD4+ T cells were injected into MHC class I plus class II-disparate F1 mice, autoimmune phenomena did not develop and alternatively a profound immunosuppressive state was induced. Furthermore, ongoing autoimmune-like GVHR induced by CD4+ T cells was also suppressed by later injection of CD8+ T cells. In these mice, an increase of donor type CD8+ T cells and a marked decrease of host B and T cells in the spleen were observed. The spleen cells from these mice strongly inhibited the mitogenic response of normal spleen cells against lipopolysaccharide (LPS). In vitro studies demonstrated that this immunosuppression was not induced by CD8+ T cells themselves but by macrophages which produced suppressive factor(s) by LPS stimulation. These findings were discussed with reference to suppressive mechanisms of GVHR.

摘要

在之前的一份报告中,我们表明将亲代CD4+ T细胞注射到主要组织相容性复合体(MHC)II类不相容的F1杂交小鼠中会诱发类似自身免疫的移植物抗宿主反应(GVHR),类似于系统性红斑狼疮(SLE)和原发性胆汁性肝硬化(PBC)的肝脏病变。在本研究中,我们检测了同时或随后注射CD8+ T细胞是否会改变GVHR的形式。当将亲代CD8+ T细胞与CD4+ T细胞一起注射到MHC I类加II类不相容的F1小鼠中时,并未出现自身免疫现象,相反,诱导出了一种深度免疫抑制状态。此外,后期注射CD8+ T细胞也抑制了由CD4+ T细胞诱导的正在进行的类似自身免疫的GVHR。在这些小鼠中,观察到脾脏中供体类型CD8+ T细胞增加,宿主B细胞和T细胞显著减少。这些小鼠的脾细胞强烈抑制正常脾细胞对脂多糖(LPS)的促有丝分裂反应。体外研究表明,这种免疫抑制不是由CD8+ T细胞本身诱导的,而是由经LPS刺激产生抑制因子的巨噬细胞诱导的。结合GVHR的抑制机制对这些发现进行了讨论。

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