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首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Costimulation Blockade followed by a 12-Week Period of Cyclosporine A Facilitates Prolonged Drug-Free Survival of Rhesus Monkey Kidney Allografts.
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Costimulation Blockade followed by a 12-Week Period of Cyclosporine A Facilitates Prolonged Drug-Free Survival of Rhesus Monkey Kidney Allografts.

机译:共刺激封锁,然后进行12周的环孢菌素A促进恒河猴肾脏同种异体移植物的长期无毒存活。

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摘要

Costimulation blockade as a single immunosuppressive treatment modality is not sufficient to prevent graft rejection. Here, we report an induction therapy using antagonistic antibodies against CD40 and CD86, given twice weekly from day -1 until day 56, followed by a delayed 12-week course of low-dose cyclosporine A (CsA) treatment in the rhesus monkey kidney-allograft model. Low-dose CsA treatment was initiated on day 42 and tapered until total cessation of all treatment on day 126. Treatment with anti-CD40/86 alone resulted in graft survival of 61, 71, 75, 78, and 116 days. Costimulation blockade followed by CsA resulted in more than 3-year drug-free survival in two of four animals. None of the animals developed donor-specific alloantibodies. Transforming growth factor-beta producing cells are present in early as well as in late kidney-graft biopsies and could play a role in the observed long-term drug-free graft survival.
机译:作为单一免疫抑制治疗手段的共刺激封锁不足以防止移植物排斥。在这里,我们报告了使用抗CD40和CD86拮抗抗体的诱导疗法,从第-1天到第56天每周两次,之后在恒河猴肾脏中低剂量的环孢素A(CsA)治疗延迟了12周疗程,同种异体移植模型。低剂量CsA治疗在第42天开始,逐渐减少直至所有治疗在第126天全部停止。单独使用抗CD40 / 86进行治疗可导致61、71、75、78和116天的移植物存活。在CsA之后进行共刺激封锁,导致四只动物中的两只有3年以上的无毒生存期。没有动物产生供体特异性同种抗体。产生转化生长因子-β的细胞存在于早期和晚期肾移植活检中,并可能在观察到的长期无药物移植存活中发挥作用。

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