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β2-微球蛋白特异性自身抗体对人外周淋巴细胞EA结合的干扰;对B细胞的抑制及对T淋巴细胞Fc受体的增强作用。

Interference of beta 2-microglobulin specific autoantibodies with EA-binding of human peripheral lymphocytes; inhibition of B-cell and enhancement of T-lymphocyte Fc-receptors.

作者信息

Falus A, Erdei A, Merétey K, Gergely J

出版信息

Immunol Lett. 1981 Oct;3(4):215-20. doi: 10.1016/0165-2478(81)90077-8.

Abstract

The effect of anti-beta 2 m-specific autoantibodies was investigated on the FcRs of human PBMCs. Anti-beta 2 m autoantibodies inhibited the FcRs of the lymphocyte subpopulation detectable by rosetting with EA(hu). On the contrary, when EA(ox) indicator system was used, in the majority of the cases an enhancement of EA rosette formation was detected. Using separated lymphocyte subpopulations we found that the binding of anti-beta 2 m autoantibodies increased the number of FcR+ non-B-cells and inhibited that of B-lymphocytes.

摘要

研究了抗β2m特异性自身抗体对人外周血单个核细胞(PBMC)Fc受体的影响。抗β2m自身抗体抑制了通过与EA(人源)花环试验可检测到的淋巴细胞亚群的Fc受体。相反,当使用EA(牛源)指示系统时,在大多数情况下检测到EA花环形成增强。使用分离的淋巴细胞亚群,我们发现抗β2m自身抗体的结合增加了FcR +非B细胞的数量,并抑制了B淋巴细胞的数量。

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