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首页> 外文期刊>Cellular immunology >FoxP3+, and not CD25+, T cells increase post-transplant in islet allotransplant recipients following anti-CD25+ rATG immunotherapy
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FoxP3+, and not CD25+, T cells increase post-transplant in islet allotransplant recipients following anti-CD25+ rATG immunotherapy

机译:抗CD25 + rATG免疫疗法后,胰岛同种异体移植受体的FoxP3 +而非CD25 + T细胞增加

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Anti-CD25 antibodies are used as an induction therapy in islet allotransplantation for type 1 diabetes. Although previous reports suggested that anti-CD25 treatment may lead to depletion of CD4+CD25+ regulatory T cells (Tregs) and questioned its use in tolerance-promoting protocols for transplantation, the effect of anti-CD25 antibodies on the frequency and function of Tregs remains unclear. We examined the effect of anti-CD25 antibody, daclizumab, in vivo on Tregs in islet allograft recipients enrolled in a single-center study and monitored post-transplant. Our data shows that the reduction in CD25+ Treg cells observed post-transplant is due to masking of CD25 receptor by daclizumab and not due to depletion. In addition, using Treg marker, FoxP3, we show that anti-CD25+ ATG treatment leads to an increase in FoxP3+ Tregs post-transplant. These data suggest that anti-CD25-based therapy has beneficial effects on Tregs and combined with ATG may be a promising therapy for autoimmunity and transplantation.
机译:抗CD25抗体在胰岛同种异体移植中用于1型糖尿病的诱导治疗。尽管先前的报道表明抗CD25治疗可能导致CD4 + CD25 +调节性T细胞(Tregs)耗竭,并质疑其在促进耐受性的移植方案中的用途,但抗CD25抗体对Tregs频率和功能的影响仍然存在不清楚。我们在单中心研究中检测了胰岛同种异体移植受者体内抗CD25抗体达珠单抗在体内对Treg的影响,并监测了移植后的情况。我们的数据表明,移植后观察到的CD25 + Treg细胞减少是由于达克里珠单抗掩盖了CD25受体,而不是由于耗竭。此外,使用Treg标记FoxP3,我们显示抗CD25 + ATG处理导致移植后FoxP3 + Treg的增加。这些数据表明,基于抗CD25的疗法对Treg具有有益作用,并且与ATG联合使用可能是一种有希望的自身免疫和移植疗法。

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