Institute for Vascular Biology, Centre for Physiology and Pharmacology, Medical University Vienna, 1090 Vienna, Austria; Christian Doppler Laboratory for Arginine Metabolism in Rheumatoid Arthritis and Multiple Sclerosis, Vienna, Austria.
Institute for Vascular Biology, Centre for Physiology and Pharmacology, Medical University Vienna, 1090 Vienna, Austria; Christian Doppler Laboratory for Arginine Metabolism in Rheumatoid Arthritis and Multiple Sclerosis, Vienna, Austria.
STAR Protoc. 2022 Aug 26;3(3):101653. doi: 10.1016/j.xpro.2022.101653. eCollection 2022 Sep 16.
By their capacity to induce peripheral T cell tolerance, dendritic cells (DCs) present a promising target cell and therapeutic strategy for treatment of several autoimmune diseases including multiple sclerosis (MS). This protocol describes how to determine the tolerogenic capacities of DCs in the context of the murine MS model, experimental autoimmune encephalomyelitis (EAE). We provide a step-by-step instruction for EAE induction, antigen-loaded bone-marrow-derived-DC (BM-DC) generation, adoptive cell transfer, and analysis of DC-mediated changes in regulatory T cell populations. For complete details on the use and execution of this protocol, please refer to Vogel et al. (2022).
树突状细胞 (DCs) 具有诱导外周 T 细胞耐受的能力,是治疗包括多发性硬化症 (MS) 在内的多种自身免疫性疾病的有前途的靶细胞和治疗策略。本方案描述了如何在实验性自身免疫性脑脊髓炎 (EAE) 即鼠 MS 模型的背景下确定 DC 的耐受能力。我们提供了诱导 EAE、负载抗原的骨髓来源树突状细胞 (BM-DC) 生成、过继性细胞转移以及分析 DC 介导的调节性 T 细胞群体变化的分步说明。有关使用和执行本方案的完整详细信息,请参阅 Vogel 等人。(2022)。