自身免疫
同种免疫
神经炎症
实验性自身免疫性脑脊髓炎
免疫学
肿瘤坏死因子α
免疫系统
生物
炎症
标识
DOI:10.3389/fimmu.2015.00364
摘要
Tumor necrosis factor superfamily (TNFSF) molecules play an important role in the activation, proliferation, differentiation and migration of immune cells into the central nervous system (CNS). Several TNF superfamily molecules are known to control alloimmunity, autoimmunity and immunity. Development of transgenic and gene knockout animals, and monoclonal antibodies against TNFSF molecules have increased our understanding of individual receptor-ligand interactions, and their intracellular signaling during homeostasis and neuroinflammation. A strong clinical association has been observed between TNFSF members and CNS autoimmunity such as multiple sclerosis (MS) and also in its animal model experimental autoimmune encephalomyelitis (EAE). Therefore, they are promising targets for alternative therapeutic options to control autoimmunity. Although, TNFSF ligands are widely distributed and have diverse functions, we have restricted the discussions in this review to TNFSF receptor-ligand interactions and their role in the pathogenesis of neuroinflammation and CNS autoimmunity.
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