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首页> 外文期刊>Transfusion: The Journal of the American Association of Blood Banks >Development of complement therapeutics for inhibition of immune-mediated red cell destruction.
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Development of complement therapeutics for inhibition of immune-mediated red cell destruction.

机译:开发用于抑制免疫介导的红细胞破坏的补体疗法。

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摘要

A major objective of my National Blood Foundation (NBF)-funded proposal was to produce recombinant soluble forms of a complement regulatory protein called complement receptor 1 (CR1) that carries the Knops blood group system antigens to perform antibody neutralization studies. By generating these recombinant proteins, we were able to inhibit several Knops antibodies in patient serum samples, thereby demonstrating their usefulness for clinical use. Interestingly, the recombinant CR1 proteins generated through NBF funding were also found to strongly reduce complement-mediated red cell destruction in a mouse hemolytic transfusion model. In this review, I will outline our NBF-funded studies, give an overview of recent advances from our group and others in the development of complement therapeutics, and highlight their potential use in the transfusion medicine setting.
机译:我的美国国家血液基金会(NBF)资助的提案的主要目标是生产称为补体受体1(CR1)的补体调节蛋白的重组可溶性形式,该蛋白携带Knops血型系统抗原来进行抗体中和研究。通过产生这些重组蛋白,我们能够抑制患者血清样品中的几种Knops抗​​体,从而证明了其在临床上的有用性。有趣的是,在小鼠溶血性输血模型中,还发现通过NBF资金产生的重组CR1蛋白可强烈减少补体介导的红细胞破坏。在这篇评论中,我将概述由NBF资助的研究,概述本小组和其他人在补体疗法发展方面的最新进展,并重点介绍其在输血医学领域的潜在用途。

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