J. Adair, D. Athwal, M. Bodmer, S. Bright, A. Collins, V. Pulito, P. Rao, R. Reedman, A. Rothermel, D. Xu
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引用次数: 58
Abstract
OKT3 is a murine monoclonal antibody which recognizes an epitope on the epsilon-subunit within the human CD3 complex. OKT3 possesses potent immunosuppressive properties in vivo and has been proven effective in the treatment of renal, heart and liver allograft rejection. Despite its efficacy, significant problems remain associated with OKT3 therapy, i.e. T-cell activation and the anti-murine antibody response. To address the problem of the anti-murine antibody response we have constructed humanized versions of OKT3. One of the humanized derivatives, gOKT3-7 incorporating the OKT3 complementarity determining regions plus a small number of alterations to the human framework, has an affinity of 1.4 x 10(9) M-1 compared with 1.2 x 10(9) M-1 for the murine OKT3. A humanized antibody (gOKT3-1) incorporating only the CDRs from OKT3 was found to be functionally inactive, confirming the requirement for nonCDR substitutions. gOKT3-7 retains the ability of mOKT3 to induce T cell proliferation in vitro and appears to be a good candidate for further development for in vivo therapy.
OKT3是一种小鼠单克隆抗体,可识别人CD3复合物内epsilon-亚基上的表位。OKT3在体内具有强大的免疫抑制特性,并已被证明在治疗肾、心和肝同种异体移植排斥反应中有效。尽管OKT3治疗有效,但仍存在显著的问题,即t细胞活化和抗小鼠抗体反应。为了解决抗小鼠抗体反应的问题,我们构建了人源化的OKT3。其中一种人源化衍生物gOKT3-7包含了OKT3的互补决定区域,加上对人类框架的少量改变,其亲和力为1.4 x 10(9) M-1,而小鼠OKT3的亲和力为1.2 x 10(9) M-1。一种人源化抗体(gOKT3-1)仅含有来自OKT3的cdr,其功能失活,证实了非cdr替代的必要性。gOKT3-7在体外保留了mOKT3诱导T细胞增殖的能力,似乎是进一步开发体内治疗的良好候选者。