RETRACTED: Chronic cardiac allograft rejection in mice is alleviated by inhibition of CCR5 in combination with cyclosporine A.

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

Abstract

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.

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。
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
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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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