Department of Microbiology and Immunology, Thomas Jefferson University, 1020 Locust St., Philadelphia, PA 19107, USA.
Immunol Res. 2011 Dec;51(2-3):134-44. doi: 10.1007/s12026-011-8259-1.
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.
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。