Casanova Jean-Laurent, Peel Jessica, Donadieu Jean, Neehus Anna-Lena, Puel Anne, Bastard Paul
St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, New York, NY, USA.
Howard Hughes Medical Institute, New York, NY, USA.
Nat Immunol. 2024 May;25(5):743-754. doi: 10.1038/s41590-024-01815-y. Epub 2024 May 2.
Human autoimmunity against elements conferring protective immunity can be symbolized by the 'ouroboros', a snake eating its own tail. Underlying infection is autoimmunity against three immunological targets: neutrophils, complement and cytokines. Autoantibodies against neutrophils can cause peripheral neutropenia underlying mild pyogenic bacterial infections. The pathogenic contribution of autoantibodies against molecules of the complement system is often unclear, but autoantibodies specific for C3 convertase can enhance its activity, lowering complement levels and underlying severe bacterial infections. Autoantibodies neutralizing granulocyte-macrophage colony-stimulating factor impair alveolar macrophages, thereby underlying pulmonary proteinosis and airborne infections, type I interferon viral diseases, type II interferon intra-macrophagic infections, interleukin-6 pyogenic bacterial diseases and interleukin-17A/F mucocutaneous candidiasis. Each of these five cytokine autoantibodies underlies a specific range of infectious diseases, phenocopying infections that occur in patients with the corresponding inborn errors. In this Review, we analyze this ouroboros of immunity against immunity and posit that it should be considered as a factor in patients with unexplained infection.
人类针对赋予保护性免疫的成分产生的自身免疫,可以用“衔尾蛇”来象征,即一条蛇在吃自己的尾巴。潜在感染是针对三种免疫靶点的自身免疫:中性粒细胞、补体和细胞因子。抗中性粒细胞自身抗体可导致轻度化脓性细菌感染所潜在的外周血中性粒细胞减少。针对补体系统分子的自身抗体的致病作用往往不明确,但针对C3转化酶的特异性自身抗体可增强其活性,降低补体水平,并导致严重细菌感染。中和粒细胞-巨噬细胞集落刺激因子的自身抗体损害肺泡巨噬细胞,从而导致肺蛋白沉积症和空气传播感染、I型干扰素病毒性疾病、II型干扰素巨噬细胞内感染、白细胞介素-6化脓性细菌疾病以及白细胞介素-17A/F黏膜皮肤念珠菌病。这五种细胞因子自身抗体中的每一种都导致特定范围的传染病,模拟相应先天性缺陷患者中发生的感染。在本综述中,我们分析了这种免疫针对免疫的衔尾蛇现象,并认为应将其视为不明原因感染患者的一个因素。