A plasmid-encoded peptide from Staphylococcus aureus induces anti-myeloperoxidase nephritogenic autoimmunity

金黄色葡萄球菌质粒编码肽诱导抗髓过氧化物酶肾炎性自身免疫

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作者:Joshua D Ooi ,Jhih-Hang Jiang ,Peter J Eggenhuizen ,Ling L Chua ,Mirjan van Timmeren ,Khai L Loh ,Kim M O'Sullivan ,Poh Y Gan ,Yong Zhong ,Kirill Tsyganov ,Lani R Shochet ,Jessica Ryan ,Coen A Stegeman ,Lars Fugger ,Hugh H Reid ,Jamie Rossjohn ,Peter Heeringa ,Stephen R Holdsworth ,Anton Y Peleg ,A Richard Kitching

Abstract

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 (MPO409-428), can induce anti-MPO autoimmunity. The peptide (6PGD391-410) 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 6PGD391-410, or with S. aureus containing a plasmid expressing 6PGD391-410, 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 6PGD391-410 is immunogenic in humans, as healthy human and AAV patient sera contain anti-6PGD and anti-6PGD391-410 antibodies. Therefore, our results support the idea that bacterial plasmids might have a function in autoimmune disease.

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