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Peripheral deletion of mature alloreactive B cells induced by costimulation blockade

机译:共刺激封锁诱导的成熟同种异体反应性B细胞的外周缺失

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摘要

Alloreactive B cells can contribute to graft rejection. Anti-CD 154 treatment together with donor-specific transfusion (DST) results in the long-term survival of MHC-mismatched mouse heart grafts and inhibition of alloantibody production. To characterize the mechanism of B cell tolerance induced by the anti-CD 154 and DST, we used 3-83Igi mice, on BALB/c (H-2K~d) background, that express a B cell receptor that reacts with MHC class Ⅰ antigens H-2K~b. Transplanting C57BL/6 (H-2K~b) hearts into 3-83lgi mice, followed by tolerance induction, resulted in the peripheral deletion of mature but not immature 3-83 B cells. The sustained deletion of mature alloreactive B cells required the presence of the allograft and can be explained by the absence of T cell help.
机译:同种反应性B细胞可导致移植排斥。抗CD 154处理与供体特异性输血(DST)一起可导致MHC不匹配的小鼠心脏移植物的长期存活,并抑制同种抗体的产生。为了描述抗CD 154和DST诱导的B细胞耐受机制,我们在BALB / c(H-2K〜d)背景下使用了3-83Igi小鼠,该小鼠表达与MHCⅠ类反应的B细胞受体抗原H-2K〜b。将C57BL / 6(H-2K〜b)心脏移植到3-83lgi小鼠中,然后诱导耐受,导致成熟但未成熟的3-83 B细胞周围缺失。成熟的同种异体反应性B细胞的持续缺失需要同种异体移植物的存在,并且可以通过缺乏T细胞的帮助来解释。

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