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在肝脏中表达H-2Kb的转基因小鼠中自身反应性CD8 + T细胞的外周清除。

Peripheral deletion of autoreactive CD8+ T cells in transgenic mice expressing H-2Kb in the liver.

作者信息

Bertolino P, Heath W R, Hardy C L, Morahan G, Miller J F

机构信息

Walter and Eliza Hall Institute of Medical Research, P.O. Royal Melbourne Hospital, Victoria, Australia.

出版信息

Eur J Immunol. 1995 Jul;25(7):1932-42. doi: 10.1002/eji.1830250721.

Abstract

The response of T cells specific for liver antigens was examined in transgenic mice expressing the allogeneic major histocompatibility complex class I molecule H-2Kb (Kb) under the control of the sheep metallothionein promoter (Met-Kb mice). To follow the fate of Kb-specific T cells, and to prevent any aberrant thymic expression of the Kb transgene, the mice were thymectomized, lethally irradiated, protected with bone marrow cells from transgenic mice expressing in their T cells a Kb-specific T cell receptor identifiable by a clonotypic antibody, and given syngeneic non-transgenic thymus grafts. Although Kb-specific CD8+ T cells were produced in the thymus grafts of these manipulated Met-Kb mice, only small numbers of such cells could be detected in the spleen and lymph nodes. The livers, however, showed signs of damage and were heavily infiltrated by actively dividing CD8+ T cells. We provide strong evidence that the hepatocytes, not generally regarded as antigen-presenting cells, activated the Kb-specific CD8+ T cells and that these disappeared after a vigorous autoimmune response that resulted in deletion.

摘要

在由绵羊金属硫蛋白启动子(Met-Kb小鼠)控制下表达同种异体主要组织相容性复合体I类分子H-2Kb(Kb)的转基因小鼠中,检测了对肝脏抗原具有特异性的T细胞反应。为了追踪Kb特异性T细胞的命运,并防止Kb转基因在胸腺中出现异常表达,对小鼠进行胸腺切除、致死性照射,用来自在其T细胞中表达可被克隆型抗体识别的Kb特异性T细胞受体的转基因小鼠的骨髓细胞进行保护,并给予同基因非转基因胸腺移植。尽管在这些经过处理的Met-Kb小鼠的胸腺移植中产生了Kb特异性CD8+T细胞,但在脾脏和淋巴结中只能检测到少量此类细胞。然而,肝脏出现了损伤迹象,并被活跃分裂的CD8+T细胞大量浸润。我们提供了有力证据,表明通常不被视为抗原呈递细胞的肝细胞激活了Kb特异性CD8+T细胞,并且这些细胞在导致细胞缺失的强烈自身免疫反应后消失。

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