Complement Research Group, Hospital La Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, Spain.
Center for Biomedical Network Research on Rare Diseases (CIBERER U754), Madrid, Spain.
Front Immunol. 2019 Apr 24;10:886. doi: 10.3389/fimmu.2019.00886. eCollection 2019.
Nephritic factors comprise a heterogeneous group of autoantibodies against neoepitopes generated in the C3 and C5 convertases of the complement system, causing its dysregulation. Classification of these autoantibodies can be clustered according to their stabilization of different convertases either from the classical or alternative pathway. The first nephritic factor described with the capacity to stabilize C3 convertase of the alternative pathway was C3 nephritic factor (C3NeF). Another nephritic factor has been characterized by the ability to stabilize C5 convertase of the alternative pathway (C5NeF). In addition, there are autoantibodies against assembled C3/C5 convertase of the classical and lectin pathways (C4NeF). These autoantibodies have been mainly associated with kidney diseases, like C3 glomerulopathy and immune complex-associated-membranoproliferative glomerulonephritis. Other clinical situations where these autoantibodies have been observed include infections and autoimmune disorders such as systemic lupus erythematosus and acquired partial lipodystrophy. C3 hypocomplementemia is a common finding in all patients with nephritic factors. The methods to measure nephritic factors are not standardized, technically complex, and lack of an appropriate quality control. This review will be focused in the description of the mechanism of action of the three known nephritic factors (C3NeF, C4NeF, and C5NeF), and their association with human diseases. Moreover, we present an overview regarding the diagnostic tools for its detection, and the main therapeutic approach for the patients with nephritic factors.
肾炎因子包括一组针对补体系统 C3 和 C5 转化酶中新表位的自身抗体,这些自身抗体导致补体系统失调。这些自身抗体的分类可以根据它们稳定不同转化酶的能力进行聚类,这些转化酶来自经典途径或替代途径。描述的第一个具有稳定替代途径 C3 转化酶能力的肾炎因子是 C3 肾炎因子 (C3NeF)。另一种肾炎因子的特征是能够稳定替代途径的 C5 转化酶 (C5NeF)。此外,还有针对经典途径和凝集素途径组装的 C3/C5 转化酶的自身抗体 (C4NeF)。这些自身抗体主要与肾脏疾病有关,如 C3 肾小球病和免疫复合物相关性膜增殖性肾小球肾炎。其他观察到这些自身抗体的临床情况包括感染和自身免疫性疾病,如系统性红斑狼疮和获得性部分脂肪营养不良。所有肾炎因子患者均存在 C3 补体血症降低。测量肾炎因子的方法尚未标准化,技术复杂,缺乏适当的质量控制。本综述将重点介绍三种已知肾炎因子 (C3NeF、C4NeF 和 C5NeF) 的作用机制及其与人类疾病的关系。此外,我们还概述了其检测的诊断工具以及肾炎因子患者的主要治疗方法。