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Mayo 诊所膜性肾病共识报告:新型分类建议。

Mayo Clinic Consensus Report on Membranous Nephropathy: Proposal for a Novel Classification.

机构信息

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.

Section of Nephrology, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.

出版信息

Mayo Clin Proc. 2023 Nov;98(11):1671-1684. doi: 10.1016/j.mayocp.2023.08.006. Epub 2023 Oct 5.

DOI:10.1016/j.mayocp.2023.08.006
PMID:37804268
Abstract

Membranous nephropathy (MN) is a pattern of injury caused by autoantibodies binding to specific target antigens, with accumulation of immune complexes along the subepithelial region of glomerular basement membranes. The past 20 years have brought revolutionary advances in the understanding of MN, particularly via the discovery of novel target antigens and their respective autoantibodies. These discoveries have challenged the traditional classification of MN into primary and secondary forms. At least 14 target antigens have been identified, accounting for 80%-90% of cases of MN. Many of the forms of MN associated with these novel MN target antigens have distinctive clinical and pathologic phenotypes. The Mayo Clinic consensus report on MN proposes a 2-step classification of MN. The first step, when possible, is identification of the target antigen, based on a multistep algorithm and using a combination of serology, staining of the kidney biopsy tissue by immunofluorescence or immunohistochemistry, and/or mass spectrometry methodology. The second step is the search for a potential underlying disease or associated condition, which is particularly relevant when knowledge of the target antigen is available to direct it. The meeting acknowledges that the resources and equipment required to perform the proposed testing may not be generally available. However, the meeting consensus was that the time has come to adopt an antigen-based classification of MN because this approach will allow for accurate and specific MN diagnosis, with significant implications for patient management and targeted treatment.

摘要

膜性肾病(MN)是一种由自身抗体与特定靶抗原结合引起的损伤模式,免疫复合物在肾小球基底膜的上皮下区域积聚。在过去的 20 年中,对 MN 的认识取得了革命性的进展,特别是通过发现新的靶抗原及其各自的自身抗体。这些发现挑战了 MN 的传统分类为原发性和继发性形式。至少已经确定了 14 个靶抗原,占 MN 病例的 80%-90%。与这些新型 MN 靶抗原相关的许多 MN 形式具有独特的临床和病理表型。Mayo 诊所关于 MN 的共识报告提出了 MN 的两步分类。第一步,在可能的情况下,根据多步算法,结合血清学、免疫荧光或免疫组织化学染色肾脏活检组织和/或质谱方法,确定靶抗原。第二步是寻找潜在的疾病或相关情况,当有靶抗原的知识可用于指导时,这一点尤为重要。会议承认,执行建议测试所需的资源和设备可能不是普遍可用的。然而,会议的共识是,现在是时候采用基于抗原的 MN 分类了,因为这种方法将允许进行准确和具体的 MN 诊断,这对患者管理和靶向治疗具有重要意义。

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