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蛋白水解作用破坏了对完整的 α345(IV)胶原的耐受性,引发了针对 α345NC1 六聚体的新型抗肾小球基底膜自身抗体。

Proteolysis breaks tolerance toward intact α345(IV) collagen, eliciting novel anti-glomerular basement membrane autoantibodies specific for α345NC1 hexamers.

机构信息

Division of Nephrology, Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.

出版信息

J Immunol. 2013 Feb 15;190(4):1424-32. doi: 10.4049/jimmunol.1202204. Epub 2013 Jan 9.

Abstract

Goodpasture disease is an autoimmune kidney disease mediated by autoantibodies against noncollagenous domain 1 (NC1) monomers of α3(IV) collagen that bind to the glomerular basement membrane (GBM), usually causing rapidly progressive glomerulonephritis (GN). We identified a novel type of human IgG4-restricted anti-GBM autoantibodies associated with mild nonprogressive GN, which specifically targeted α345NC1 hexamers but not α3NC1 monomers. The mechanisms eliciting these anti-GBM autoantibodies were investigated in mouse models recapitulating this phenotype. Wild-type and FcγRIIB(-/-) mice immunized with autologous murine GBM NC1 hexamers produced mouse IgG1-restricted autoantibodies specific for α345NC1 hexamers, which bound to the GBM in vivo but did not cause GN. In these mice, intact collagen IV from murine GBM was not immunogenic. However, in Col4a3(-/-) Alport mice, both intact collagen IV and NC1 hexamers from murine GBM elicited IgG Abs specific for α345NC1 hexamers, which were not subclass restricted. As heterologous Ag in COL4A3-humanized mice, murine GBM NC1 hexamers elicited mouse IgG1, IgG2a, and IgG2b autoantibodies specific for α345NC1 hexamers and induced anti-GBM Ab GN. These findings indicate that tolerance toward autologous intact α345(IV) collagen is established in hosts expressing this Ag, even though autoreactive B cells specific for α345NC1 hexamers are not purged from their repertoire. Proteolysis selectively breaches this tolerance by generating autoimmunogenic α345NC1 hexamers. This provides a mechanism eliciting autoantibodies specific for α345NC1 hexamers, which are restricted to noninflammatory IgG subclasses and are nonnephritogenic. In Alport syndrome, lack of tolerance toward α345(IV) collagen promotes production of alloantibodies to α345NC1 hexamers, including proinflammatory IgG subclasses that mediate posttransplant anti-GBM nephritis.

摘要

Goodpasture 病是一种由针对 α3(IV) 胶原非胶原域 1(NC1) 单体的自身抗体介导的自身免疫性肾病,这些自身抗体与肾小球基底膜(GBM)结合,通常导致快速进行性肾小球肾炎(GN)。我们鉴定了一种新型的与人 IgG4 受限的抗 GBM 自身抗体相关的轻度非进行性 GN,该自身抗体特异性靶向 α345NC1 六聚体,但不靶向 α3NC1 单体。在模拟这种表型的小鼠模型中研究了引发这些抗 GBM 自身抗体的机制。用自体鼠 GBM NC1 六聚体免疫的野生型和 FcγRIIB(-/-)小鼠产生了特异性针对 α345NC1 六聚体的小鼠 IgG1 受限的自身抗体,这些自身抗体在体内与 GBM 结合,但不会引起 GN。在这些小鼠中,来自鼠 GBM 的完整胶原 IV 没有免疫原性。然而,在 Col4a3(-/-)Alport 小鼠中,来自鼠 GBM 的完整胶原 IV 和 NC1 六聚体都能引发针对 α345NC1 六聚体的 IgG Abs,且不受亚类限制。作为 COL4A3 人源化小鼠中的异源 Ag,鼠 GBM NC1 六聚体引发了针对 α345NC1 六聚体的特异性的小鼠 IgG1、IgG2a 和 IgG2b 自身抗体,并诱导抗 GBM Ab GN。这些发现表明,即使针对 α345NC1 六聚体的自身反应性 B 细胞未从其库中清除,在表达该 Ag 的宿主中也会建立对自身完整 α345(IV)胶原的耐受。蛋白水解选择性地通过产生自身免疫性的 α345NC1 六聚体来打破这种耐受。这为引发针对 α345NC1 六聚体的自身抗体提供了一种机制,这些自身抗体仅限于非炎症性 IgG 亚类,且不会引起肾炎。在 Alport 综合征中,对 α345(IV)胶原的耐受缺失会促进针对 α345NC1 六聚体的同种异体抗体的产生,包括介导移植后抗 GBM 肾炎的促炎 IgG 亚类。

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