Centre for Inflammatory Diseases, Monash University Department of Medicine, Monash Medical Centre, Clayton, VIC, 3168, Australia.
Infection and Immunity Program, Monash Biomedicine Discovery Institute and Department of Microbiology, Monash University, Clayton, VIC, 3800, Australia.
Nat Commun. 2019 Jul 29;10(1):3392. doi: 10.1038/s41467-019-11255-0.
Autoreactivity to myeloperoxidase (MPO) causes anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV), with rapidly progressive glomerulonephritis. Here, we show that a Staphylococcus aureus peptide, homologous to an immunodominant MPO T-cell epitope (MPO), can induce anti-MPO autoimmunity. The peptide (6PGD) is part of a plasmid-encoded 6-phosphogluconate dehydrogenase found in some S. aureus strains. It induces anti-MPO T-cell autoimmunity and MPO-ANCA in mice, whereas related sequences do not. Mice immunized with 6PGD, or with S. aureus containing a plasmid expressing 6PGD, develop glomerulonephritis when MPO is deposited in glomeruli. The peptide induces anti-MPO autoreactivity in the context of three MHC class II allomorphs. Furthermore, we show that 6PGD is immunogenic in humans, as healthy human and AAV patient sera contain anti-6PGD and anti-6PGD antibodies. Therefore, our results support the idea that bacterial plasmids might have a function in autoimmune disease.
髓过氧化物酶(MPO)自身反应性导致抗中性粒细胞胞质抗体(ANCA)相关性血管炎(AAV),伴有快速进行性肾小球肾炎。在这里,我们表明,金黄色葡萄球菌肽与免疫优势 MPO T 细胞表位(MPO)同源,可诱导抗 MPO 自身免疫。该肽(6PGD)是一些金黄色葡萄球菌菌株中质粒编码的 6-磷酸葡萄糖酸脱氢酶的一部分。它在小鼠中诱导抗 MPO T 细胞自身免疫和 MPO-ANCA,而相关序列则不会。用 6PGD 免疫或用表达 6PGD 的质粒表达的金黄色葡萄球菌免疫的小鼠,当 MPO 沉积在肾小球中时会发展为肾小球肾炎。该肽在三种 MHC Ⅱ类同种异型的背景下诱导抗 MPO 自身反应性。此外,我们表明 6PGD 在人类中具有免疫原性,因为健康人类和 AAV 患者的血清中含有抗 6PGD 和抗 6PGD 抗体。因此,我们的结果支持细菌质粒可能在自身免疫性疾病中发挥作用的观点。