排斥反应抑制 CCR5 与环孢素 A 联用可减轻小鼠慢性心脏异体移植排斥反应。

IF 0.5 4区 管理学 Q3 INFORMATION SCIENCE & LIBRARY SCIENCE
Jun Li, Kailun Zhang, Jiahong Xia
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引用次数: 0

摘要

趋化因子受体 CCR5 在急性移植物排斥反应中发挥着重要作用。在这项研究中,我们研究了抑制CCR5与环孢素A(CsA)联合治疗对心脏移植慢性排斥反应的影响。45名移植受者被随机分为三组。A组受者接受抗CCR5 mAb和CsA治疗,B组小鼠仅接受抗CCR5 mAb治疗,C组动物仅接受CsA治疗。移植后第 45 天,收获异体移植物并用免疫组织学技术和 PT-PCR 方法进行检查。接受抗 CCR5 mAb 和 CsA 治疗的异体移植物存活时间明显延长(44.73 ± 0.258 天,P
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RETRACTED: Chronic cardiac allograft rejection in mice is alleviated by inhibition of CCR5 in combination with cyclosporine A.

The chemokine receptor CCR5 plays important roles in acute allograft rejection. In this study, we examined the inhibition of CCR5 in combination with the treatment with cyclosporine A (CsA) in chronic rejection in cardiac transplantation. Forty-five transplant recipients were randomized to three groups. Recipients in group A were treated with anti-CCR5 mAb and CsA, mice in group B were given anti-CCR5 mAb alone, and animals in group C were administered with only CsA. On day 45 after transplantation, the allografts were harvested and examined by immunohistologic technique and PT-PCR methods. Allografts treated with anti-CCR5 mAb and CsA showed significantly prolonged survival (44.73 ± 0.258 days, P < 0.01) as compared with CsA-treated group (37.00 ± 2.04 days). Treatment with anti-CCR5 mAb plus CsA significantly inhibited the progression of cardiac allograft vasculopathy. Our findings demonstrated that anti-CCR5 mAb in combination with CsA can prolong the survival of allograft through their cardio-protective and immunomodulative properties. Thus, combined administration of anti-CCR5 mAb and CsA may become a new therapeutic approach for the prevention of cardiac graft failure that has not been obviated by conventional immunosuppressive agents.

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来源期刊
Malaysian Journal of Library & Information Science
Malaysian Journal of Library & Information Science INFORMATION SCIENCE & LIBRARY SCIENCE-
CiteScore
2.00
自引率
7.70%
发文量
8
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