抗mCRP自身抗体在狼疮性肾炎中的作用。

IF 3.2 4区 医学 Q1 UROLOGY & NEPHROLOGY Kidney Diseases Pub Date : 2023-05-15 eCollection Date: 2023-10-01 DOI:10.1159/000530928
Mo Yuan, Ying Tan, Ming-Hui Zhao
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引用次数: 0

摘要

背景:狼疮性肾炎的特点是产生多种自身抗体。然而,很少有自身抗体与疾病活动性和预后相关。CRP至少以两种构象不同的形式存在:天然五聚体C-反应蛋白(pCRP)和修饰/单体CRP(mCRP)。抗mCRP自身抗体在狼疮性肾炎患者的血清中普遍存在,据报道具有致病性。综述:血清抗mCRP自身抗体水平与狼疮性肾炎患者的临床疾病活动、肾小管间质病变、治疗反应和预后有关。mCRP的关键表位是氨基酸35-47。此外,新出现的证据表明,抗mCRP自身抗体可以通过形成原位免疫复合物或干扰mCRP的生物学功能,如与补体C1q和因子H结合,参与狼疮肾炎的发病机制,以及抗mCRP自身抗体在狼疮性肾炎中的潜在发病机制,这可能为狼疮性肾炎提供一种有前景的新治疗策略。
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The Role of Anti-mCRP Autoantibodies in Lupus Nephritis.

Background: Lupus nephritis is characterized by multiple autoantibodies production. However, there are few autoantibodies associated with disease activity and prognosis. CRP exists in at least two conformationally distinct forms: native pentameric C-reactive protein (pCRP) and modified/monomeric CRP (mCRP). Autoantibodies against mCRP are prevalent in sera of patients with lupus nephritis and are reported to be pathogenic.

Summary: The levels of serum anti-mCRP autoantibodies are associated with clinical disease activity, tubulointerstitial lesions, treatment response, and prognosis in patients with lupus nephritis. The key epitope of mCRP was amino acid 35-47. Furthermore, emerging evidence indicated that anti-mCRP autoantibodies could participate in the pathogenesis of lupus nephritis by forming in situ immune complexes or interfering with the biological functions of mCRP, such as binding to complement C1q and factor H.

Key messages: Here, we review the recent advances in the prevalence, clinical-pathological associations, and potential pathogenesis of anti-mCRP autoantibodies in lupus nephritis, which may provide a promising novel therapeutic strategy for lupus nephritis.

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来源期刊
Kidney Diseases
Kidney Diseases UROLOGY & NEPHROLOGY-
CiteScore
6.00
自引率
2.70%
发文量
33
审稿时长
27 weeks
期刊介绍: ''Kidney Diseases'' aims to provide a platform for Asian and Western research to further and support communication and exchange of knowledge. Review articles cover the most recent clinical and basic science relevant to the entire field of nephrological disorders, including glomerular diseases, acute and chronic kidney injury, tubulo-interstitial disease, hypertension and metabolism-related disorders, end-stage renal disease, and genetic kidney disease. Special articles are prepared by two authors, one from East and one from West, which compare genetics, epidemiology, diagnosis methods, and treatment options of a disease.
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