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抗红细胞自身抗体转基因小鼠:自身免疫性溶血性贫血的小鼠模型。

Anti-red blood cell autoantibody transgenic mice: murine model of autoimmune hemolytic anemia.

作者信息

Murakami M, Honjo T

机构信息

Department of Medical Chemistry, Kyoto University, Japan.

出版信息

Semin Immunol. 1996 Feb;8(1):3-9. doi: 10.1006/smim.1996.0002.

Abstract

We established an anti-red blood cell (RBC) autoantibody transgenic mouse line, in which almost all B cells were deleted in the periphery. A small number of B-1 cells, however, escaped from deletion, survived and expanded in the peritoneal cavity and the gut, because of the absence of RBC. The activation of B-1 cells by enteric bacteria induced autoimmune hemolytic anemia (AIHA). In turn, AIHA was cured by elimination of peritoneal B-1 cells. This Tg mouse line is useful for revealing the generation and activation of B-1 cells, and for clarifying the physiological and pathological roles of B-1 cells.

摘要

我们建立了一种抗红细胞(RBC)自身抗体转基因小鼠品系,其中几乎所有外周B细胞均被清除。然而,由于不存在红细胞,少数B-1细胞逃脱了清除,在腹腔和肠道中存活并扩增。肠道细菌对B-1细胞的激活诱导了自身免疫性溶血性贫血(AIHA)。反过来,通过清除腹腔B-1细胞可治愈AIHA。该转基因小鼠品系有助于揭示B-1细胞的产生和激活,并阐明B-1细胞的生理和病理作用。

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