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兔抗猪胸腺细胞球蛋白对新生猪的淋巴细胞清除作用

Lymphodepletive effects of rabbit anti-pig thymocyte globulin in neonatal swines.

作者信息

Pan Hua, Gazarian Aram, Mollet Isabelle, Mathias Virginie, Dubois Valérie, Sobh Mohamad, Buff Samuel, Dubernard Jean-Michel, Michallet Mauricette, Michallet Marie-Cécile

机构信息

Université de Lyon, VetAgro Sup, Chair of Transplantation, Marcy l'Etoile, France; Plastic and Reconstructive Department, Xijing Hospital, Xi'an, China.

Université de Lyon, VetAgro Sup, Chair of Transplantation, Marcy l'Etoile, France; Hand Surgery Department, Clinique du Parc, Lyon, France.

出版信息

Transpl Immunol. 2016 Nov;39:74-83. doi: 10.1016/j.trim.2016.08.005. Epub 2016 Aug 22.

Abstract

Lymphodepletive agents play important role in different clinical applications or experimental transplant studies. In order to facilitate preclinical pediatric transplant studies, we have developed the rabbit anti-pig thymocyte globulin (pATG) and studied its effects in neonatal swines. In vitro assays showed that pATG can bind to lymphocytes and neutrophils in a dose-dependent manner and lyse peripheral blood mononuclear cells by apoptosis and complement-dependent cytotoxicity. In vivo, pATG as a monotherapy was administered at different doses (2.5, 5, 20, 40 and 80mg/kg) in newborn pigs. Results showed that pATG induced a dose-dependent but transient T-cell depletion in peripheral blood. Lymphodepletion was also observed in lymph nodes, spleen and thymus. Pharmacokinetic studies showed dose-related cell-bound pATG on lymphocytes, as well as the presence of free pATG in the serum. Both cell-bound and free pATG levels decreased gradually after administration. Interestingly, adjuvant mycophenolate mofetil (MMF) given at 1g/m/day for 1week successfully maintained pATG-induced T-cell depletion. In conclusion, pATG administration can cause transient T-cell depletion in neonatal pigs and this effect can be maintained by MMF. Therefore, we have developed an original immunosuppressive regimen that can be used for transplantation studies in swine model.

摘要

淋巴细胞清除剂在不同的临床应用或实验性移植研究中发挥着重要作用。为了促进临床前儿科移植研究,我们研发了兔抗猪胸腺细胞球蛋白(pATG)并研究了其在新生猪中的作用。体外试验表明,pATG能以剂量依赖性方式与淋巴细胞和中性粒细胞结合,并通过凋亡和补体依赖性细胞毒性作用裂解外周血单个核细胞。在体内,以不同剂量(2.5、5、20、40和80mg/kg)对新生猪单独给予pATG。结果显示,pATG在外周血中诱导了剂量依赖性但短暂的T细胞清除。在淋巴结、脾脏和胸腺中也观察到了淋巴细胞清除。药代动力学研究表明,淋巴细胞上存在剂量相关的细胞结合型pATG,血清中也存在游离的pATG。给药后,细胞结合型和游离pATG水平均逐渐下降。有趣的是,每天给予1g/m的霉酚酸酯(MMF)作为佐剂,持续1周,成功维持了pATG诱导的T细胞清除。总之,给予pATG可导致新生猪短暂的T细胞清除,且这种作用可通过MMF维持。因此,我们研发了一种可用于猪模型移植研究的原创免疫抑制方案。

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