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基于髓系调节性细胞的治疗中的调节性巨噬细胞和耐受原性树突状细胞。

Regulatory Macrophages and Tolerogenic Dendritic Cells in Myeloid Regulatory Cell-Based Therapies.

机构信息

Centre de Recherche en Transplantation et Immunologie-UMR1064, INSERM-ITUN, Nantes Université, CHU Nantes, 44000 Nantes, France.

出版信息

Int J Mol Sci. 2021 Jul 26;22(15):7970. doi: 10.3390/ijms22157970.

DOI:10.3390/ijms22157970
PMID:34360736
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8348814/
Abstract

Myeloid regulatory cell-based therapy has been shown to be a promising cell-based medicinal approach in organ transplantation and for the treatment of autoimmune diseases, such as type 1 diabetes, rheumatoid arthritis, Crohn's disease and multiple sclerosis. Dendritic cells (DCs) are the most efficient antigen-presenting cells and can naturally acquire tolerogenic properties through a variety of differentiation signals and stimuli. Several subtypes of DCs have been generated using additional agents, including vitamin D3, rapamycin and dexamethasone, or immunosuppressive cytokines, such as interleukin-10 (IL-10) and transforming growth factor-beta (TGF-β). These cells have been extensively studied in animals and humans to develop clinical-grade tolerogenic (tol)DCs. Regulatory macrophages (Mregs) are another type of protective myeloid cell that provide a tolerogenic environment, and have mainly been studied within the context of research on organ transplantation. This review aims to thoroughly describe the ex vivo generation of tolDCs and Mregs, their mechanism of action, as well as their therapeutic application and assessment in human clinical trials.

摘要

基于髓系调节细胞的治疗已被证明是一种有前途的基于细胞的医学方法,可用于器官移植和治疗自身免疫性疾病,如 1 型糖尿病、类风湿性关节炎、克罗恩病和多发性硬化症。树突状细胞 (DC) 是最有效的抗原呈递细胞,通过多种分化信号和刺激,可以自然获得耐受性。已经使用其他试剂(包括维生素 D3、雷帕霉素和地塞米松)或免疫抑制细胞因子(如白细胞介素-10 (IL-10) 和转化生长因子-β (TGF-β))生成了几种 DC 亚型。这些细胞已在动物和人类中进行了广泛研究,以开发临床级别的耐受性 (tol)DC。调节性巨噬细胞 (Mregs) 是另一种保护性髓系细胞,可提供耐受环境,主要在器官移植研究的背景下进行研究。本综述旨在全面描述 tolDC 和 Mregs 的体外生成、它们的作用机制,以及它们在人类临床试验中的治疗应用和评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8657/8348814/32150504c67e/ijms-22-07970-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8657/8348814/a411c0aa2d91/ijms-22-07970-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8657/8348814/32150504c67e/ijms-22-07970-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8657/8348814/a411c0aa2d91/ijms-22-07970-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8657/8348814/32150504c67e/ijms-22-07970-g002.jpg

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