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免疫检查点抑制剂诱导的重症肌无力患者的临床血清学见解。

Clinicoserological insights into patients with immune checkpoint inhibitor-induced myasthenia gravis.

机构信息

Department of Immunobiology, Yale School of Medicine, New Haven, Connecticut, 06511, USA.

Department of Neurology, Yale School of Medicine, New Haven, Connecticut, 06511, USA.

出版信息

Ann Clin Transl Neurol. 2023 May;10(5):825-831. doi: 10.1002/acn3.51761. Epub 2023 Mar 16.

Abstract

To compare the immunopathology of immune checkpoint inhibitor-induced myasthenia gravis (ICI-MG) and idiopathic MG, we profiled the respective AChR autoantibody pathogenic properties. Of three ICI-MG patients with AChR autoantibodies, only one showed complement activation and modulation/blocking potency, resembling idiopathic MG. In contrast, AChR autoantibody-mediated effector functions were not detected in the other two patients, questioning the role of their AChR autoantibodies as key mediators of pathology. The contrasting properties of AChR autoantibodies in these cases challenge the accuracy of serological testing in establishing definite ICI-MG diagnoses and underscore the importance of a thorough clinical assessment when evaluating ICI-related adverse events.

摘要

为了比较免疫检查点抑制剂诱导的重症肌无力(ICI-MG)和特发性 MG 的免疫病理学,我们对各自的 AChR 自身抗体的致病特性进行了分析。在 3 名患有 AChR 自身抗体的 ICI-MG 患者中,只有 1 名患者表现出补体激活和调节/阻断效力,类似于特发性 MG。相比之下,另外 2 名患者未检测到 AChR 自身抗体介导的效应功能,这对其 AChR 自身抗体作为病理主要介质的作用提出了质疑。这些病例中 AChR 自身抗体的对比特性挑战了血清学检测在确定 ICI-MG 诊断中的准确性,并强调了在评估 ICI 相关不良反应时进行全面临床评估的重要性。

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