III. Medizinische Klinik, Universitätsklinikum Hamburg-Eppendorf, Martinistraße 52, 20246, Hamburg, Germany.
Semin Immunopathol. 2018 Jul;40(4):393-406. doi: 10.1007/s00281-018-0670-4. Epub 2018 Mar 22.
Abnormal activation of the innate immune system is a common feature of autoimmune and chronic inflammatory diseases. Since their identification as a separate family of leukocytes, innate lymphoid cells (ILCs) have emerged as important effector cells of the innate immune system. Alterations in ILC function and subtype distribution have been observed in a variety of immune-mediated diseases in humans and evidence from experimental models suggests a subtype specific role of ILCs in the pathophysiology of autoimmune inflammation. In this review, we discuss recent advances in the understanding of ILC biology in autoimmune and chronic inflammatory disorders, including multiple sclerosis, inflammatory bowel diseases, psoriasis, and rheumatic diseases, with a special focus on the potential of ILCs as therapeutic targets for the development of novel treatment strategies in humans.
先天免疫系统的异常激活是自身免疫和慢性炎症性疾病的共同特征。自从它们被鉴定为白细胞的一个独立家族以来,先天淋巴细胞 (ILC) 已成为先天免疫系统的重要效应细胞。在人类的各种免疫介导性疾病中观察到 ILC 功能和亚型分布的改变,实验模型的证据表明 ILC 在自身免疫炎症的病理生理学中具有特定亚型的作用。在这篇综述中,我们讨论了自身免疫和慢性炎症性疾病(包括多发性硬化症、炎症性肠病、银屑病和风湿性疾病)中对 ILC 生物学的理解的最新进展,特别关注 ILC 作为治疗靶点的潜力,以开发人类的新型治疗策略。