Laboratory of Immunobiology, Rega Institute, Leuven, Belgium; Department of Microbiology and Immunology, KU Leuven, University of Leuven, Minderbroedersstraat 10, B-3000 Leuven, Belgium; Oxford Glycobiology Institute, University of Oxford, South Parks Road, Oxford OX1 3QU, UK.
Department of Microbiology and Immunology, KU Leuven, University of Leuven, Minderbroedersstraat 10, B-3000 Leuven, Belgium; Laboratory of Molecular Immunology, Rega Institute, Leuven, Belgium.
Trends Mol Med. 2016 Sep;22(9):746-757. doi: 10.1016/j.molmed.2016.07.002. Epub 2016 Aug 2.
Diagnosis and treatment of autoimmunity has mainly relied on adaptive immunity. Infection and inflammation induce cytokines and chemokines and activate myeloid cells to release enzymes. Proteases cleave host proteins into a molar excess of remnant peptides. Additional enzymes modify these peptides into putative autoantigens prior to T and B cell activation. We propose that post-translational modifications may be a means of generating auto-reactive peptides. Microbes also provide proteases and modifying enzymes to the host, and we posit that this may result in autoantigen generation. This could help explain, at least in part, the recently discovered connections between microbiota and autoimmunity. Better explorations of the innate prelude phase of autoimmunity in conjunction with environmental factors might provide novel, broadly applicable therapies.
自身免疫的诊断和治疗主要依赖于适应性免疫。感染和炎症会诱导细胞因子和趋化因子,并激活髓样细胞释放酶。蛋白酶将宿主蛋白切割成摩尔过量的残留肽。在 T 和 B 细胞激活之前,其他酶将这些肽修饰成潜在的自身抗原。我们提出,翻译后修饰可能是产生自身反应性肽的一种方式。微生物也向宿主提供蛋白酶和修饰酶,我们假设这可能导致自身抗原的产生。这至少可以部分解释最近发现的微生物群与自身免疫之间的联系。更好地探索自身免疫的先天前奏阶段以及环境因素可能会提供新的、广泛适用的治疗方法。