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日本猕猴免疫抑制的安全管理:与临床前异种移植研究的相关性。

Safe Administration of Immunosuppression in Japanese Monkeys: Relevance to Preclinical Xenotransplantation Studies.

作者信息

Sakata Naoaki, Yoshimatsu Gumpei, Kawakami Ryo, Kodama Shohta

机构信息

Department of Regenerative Medicine and Transplantation, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.

Center for Regenerative Medicine, Fukuoka University Hospital, Fukuoka, Japan.

出版信息

Cell Transplant. 2025 Jan-Dec;34:9636897251322295. doi: 10.1177/09636897251322295. Epub 2025 Mar 13.

Abstract

The Japanese monkey has been used in several animal studies; however, its potential as a recipient model for xenotransplantation is unclear. The potential of the Japanese monkey as a recipient for xenotransplantation was assessed using two experimental models. The first model evaluated the optimal dose of tacrolimus without severe adverse events. The plasma tacrolimus levels, blood counts, and hepatic and renal function tests were evaluated. The second model assessed the immunosuppressive effects of thymoglobulin and tacrolimus. Immunosuppression was evaluated using blood counts and flow cytometry to measure lymphocytes in peripheral blood mononuclear cells (PBMCs). In the first model, the target trough level (10-15 ng/ml) was achieved and maintained with tacrolimus administration at 1.6 mg/kg/day in all monkeys. There were no adverse events related to the blood count or to liver, kidney, or nutrient parameters at this dose, except for hemoglobin. In the second model, a decrease in white blood cells was observed. Flow cytometry revealed a temporary decrease in T- and B-cell numbers among PBMCs on day 4. We consider that the Japanese monkey is acceptable to be used as a recipient model for preclinical xenotransplantation. The safe administration of tacrolimus and thymoglobulin is clarified for this model.

摘要

日本猕猴已被用于多项动物研究;然而,其作为异种移植受体模型的潜力尚不清楚。使用两种实验模型评估了日本猕猴作为异种移植受体的潜力。第一个模型评估了无严重不良事件的他克莫司最佳剂量。评估了血浆他克莫司水平、血细胞计数以及肝肾功能测试。第二个模型评估了抗胸腺细胞球蛋白和他克莫司的免疫抑制作用。使用血细胞计数和流式细胞术评估免疫抑制,以测量外周血单个核细胞(PBMC)中的淋巴细胞。在第一个模型中,所有猕猴以1.6mg/kg/天的剂量给予他克莫司,均达到并维持了目标谷浓度(10 - 15ng/ml)。在此剂量下,除血红蛋白外,未出现与血细胞计数或肝脏、肾脏或营养参数相关的不良事件。在第二个模型中,观察到白细胞减少。流式细胞术显示第4天PBMC中T细胞和B细胞数量暂时减少。我们认为日本猕猴可作为临床前异种移植的受体模型。该模型明确了他克莫司和抗胸腺细胞球蛋白的安全给药方式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eae/12059421/57ec6b4e7749/10.1177_09636897251322295-img2.jpg

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