Ooi Joshua D, Phoon Richard K S, Holdsworth Stephen R, Kitching A Richard
Centre for Inflammatory Diseases, Monash University Department of Medicine, Monash Medical Centre, 246 Clayton Road, Clayton, VIC 3168, Australia.
J Am Soc Nephrol. 2009 May;20(5):980-9. doi: 10.1681/ASN.2008080891. Epub 2009 Apr 8.
The autoantigen in Goodpasture disease is the noncollagenous domain of alpha3 type IV collagen [alpha3(IV)NC1]. We previously demonstrated that IL-12p40(-/-) mice are protected from experimental autoimmune anti-glomerular basement membrane (anti-GBM) glomerulonephritis, seemingly defining a role for IL-12 in this disease; however, the recent identification of IL-23, a heterodimer composed of IL-12p40 and IL-23p19 subunits, raises the possibility that IL-23, rather than IL-12, may modulate this disease instead. We immunized wild-type, IL-12p35(-/-) (IL-12 deficient, IL-23 intact), IL-12p40(-/-) (deficient in both IL-12 and IL-23), and IL-23p19(-/-) (IL-12 intact, IL-23 deficient) mice with recombinant mouse alpha3(IV)NC1. Wild-type mice developed autoreactivity to alpha3(IV)NC1: Humoral responses, cellular responses, renal histologic abnormalities, leukocyte accumulation, autoantibody deposition, and IL-17A mRNA expression (a cytokine produced by the IL-23-maintained Th17 subset). IL-23 but not IL-12 was detected in the immune system. Regardless of the presence of IL-12, mice deficient in IL-23 were protected, but mice with IL-23 were not. Both IL-23-deficient strains exhibited lower autoantibody titers, reduced cellular reactivity, diminished cytokine production (IFN-gamma [Th1], IL-17A [Th17], TNF, and monocyte chemoattractant protein 1), and less renal disease and glomerular IgG deposition. The deficient responses in the absence of IL-23 were not due to increased regulatory T cells; IL-12p40(-/-) and IL-23p19(-/-) mice did not show increased proportions of CD4(+)CD25(+)FoxP3(+) cells or IL-10 levels early in the immune response. In conclusion, autoreactivity to the Goodpasture antigen is directed primarily by IL-23, absence of which results in hyporeactivity including but extending beyond a deficient Th17 response.
肺出血肾炎综合征中的自身抗原是IV型胶原α3链的非胶原结构域[α3(IV)NC1]。我们先前证明,IL-12p40(-/-)小鼠可免受实验性自身免疫性抗肾小球基底膜(抗GBM)肾小球肾炎的影响,这似乎确定了IL-12在该疾病中的作用;然而,最近发现的IL-23是一种由IL-12p40和IL-23p19亚基组成的异二聚体,这增加了一种可能性,即可能是IL-23而非IL-12调节了这种疾病。我们用重组小鼠α3(IV)NC1免疫野生型、IL-12p35(-/-)(IL-12缺陷,IL-23完整)、IL-12p40(-/-)(IL-12和IL-23均缺陷)和IL-23p19(-/-)(IL-12完整,IL-23缺陷)小鼠。野生型小鼠对α3(IV)NC1产生了自身反应性:体液反应、细胞反应、肾脏组织学异常、白细胞积聚、自身抗体沉积以及IL-17A mRNA表达(一种由IL-23维持的Th17亚群产生的细胞因子)。在免疫系统中检测到了IL-23而非IL-12。无论IL-12是否存在,IL-23缺陷的小鼠都受到了保护,而有IL-23的小鼠则没有。两种IL-23缺陷型品系均表现出较低的自身抗体滴度、降低的细胞反应性、减少的细胞因子产生(IFN-γ[Th1]、IL-17A[Th17]、TNF和单核细胞趋化蛋白1)以及较轻的肾脏疾病和肾小球IgG沉积。在没有IL-23的情况下反应缺陷并非由于调节性T细胞增加;IL-12p40(-/-)和IL-23p19(-/-)小鼠在免疫反应早期未显示CD4(+)CD25(+)FoxP3(+)细胞比例增加或IL-10水平升高。总之,对肺出血肾炎综合征抗原的自身反应性主要由IL-23介导,如果没有IL-23,则会导致反应低下,包括但不限于Th17反应缺陷。