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用于免疫抑制和诱导耐受的CD4单克隆抗体对。

CD4 monoclonal antibody pairs for immunosuppression and tolerance induction.

作者信息

Qin S, Cobbold S, Tighe H, Benjamin R, Waldmann H

出版信息

Eur J Immunol. 1987 Aug;17(8):1159-65. doi: 10.1002/eji.1830170813.

Abstract

A pair of rat anti-mouse CD4 monoclonal antibodies (mAb) have been selected which bind to different epitopes of the molecule. Both the mAb are rat IgG2b and show clear synergistic activity in complement lysis in vitro. When injected together in vivo, they exhibit an improved immunosuppressive effect, compared to each antibody alone, on allogeneic graft rejection, humoral responses and on tolerance induction. Limiting dilution analysis indicates that the in vivo depletion of interleukin 2-producing cells is improved using both mAb by 2-3-fold over that obtained with the individual antibodies. As little as 60 ng per mouse of the CD4 antibody pair was sufficient to allow the induction of tolerance to human gamma-globulin, even without elimination of the CD4+ cells. The results suggest that appropriate antibody pairs may be good candidates for effective immunosuppressive serotherapy in man.

摘要

已筛选出一对大鼠抗小鼠CD4单克隆抗体(mAb),它们与该分子的不同表位结合。这两种单克隆抗体均为大鼠IgG2b,在体外补体裂解中表现出明显的协同活性。当在体内一起注射时,与单独使用每种抗体相比,它们在同种异体移植排斥、体液反应和耐受性诱导方面表现出更好的免疫抑制效果。有限稀释分析表明,与单独使用抗体相比,同时使用这两种单克隆抗体可使产生白细胞介素2的细胞在体内的耗竭提高2至3倍。每只小鼠低至60 ng的CD4抗体对就足以诱导对人γ球蛋白的耐受性,即使不清除CD4+细胞也是如此。结果表明,合适的抗体对可能是人类有效免疫抑制血清疗法的良好候选者。

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