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调节性 T 细胞对于防止红细胞特异性自身抗体反应的小鼠模型中自身耐受的丧失至关重要。

Regulatory T cells essential to prevent the loss of self-tolerance in murine models of erythrocyte-specific autoantibody responses.

机构信息

Department of Microbiology and Immunology, Thomas Jefferson University, 1020 Locust St., Philadelphia, PA 19107, USA.

出版信息

Immunol Res. 2011 Dec;51(2-3):134-44. doi: 10.1007/s12026-011-8259-1.

Abstract

The spontaneous appearance of anti-erythrocyte autoantibodies resulting in autoimmune hemolytic anemia described in NZB mice more than 40 years ago provided a model for the study of mechanisms behind the loss of self-tolerance. We developed an in vitro model of this anti-MRBC response in which CD8(+) suppressor T cells were shown to be a controlling element. CD8(+) T cells from young NZB mice co-cultured with spleen cells from old, actively autoimmune NZB mice suppressed the anti-MRBC responses of the old mice. Eliminating the CD8(+) cells from young NZB spleen cells or even from non-autoimmune BALB/c spleen cells prior to culture removed the controlling influence of these CD8(+) cells and allowed the development of anti-MRBC-secreting cells. This review will consider the role of the CD8(+) suppressive cells in the anti-self-erythrocyte model in light of insights provided by current 'regulatory T cell' literature.

摘要

40 多年前,NZB 小鼠中自发出现的抗红细胞自身抗体导致自身免疫性溶血性贫血,为研究自身耐受丧失的机制提供了模型。我们建立了这种抗 MRBC 反应的体外模型,其中 CD8(+)抑制性 T 细胞是一个控制因素。年轻的 NZB 小鼠的 CD8(+) T 细胞与来自老年、主动自身免疫性 NZB 小鼠的脾细胞共培养,抑制了老年小鼠的抗 MRBC 反应。在培养之前从年轻的 NZB 脾细胞中去除 CD8(+)细胞,甚至从非自身免疫性 BALB/c 脾细胞中去除 CD8(+)细胞,消除了这些 CD8(+)细胞的控制作用,并允许抗-MRBC 分泌细胞的发育。这篇综述将根据当前“调节性 T 细胞”文献提供的见解,考虑 CD8(+)抑制性细胞在抗自身红细胞模型中的作用。

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