抗粒细胞-巨噬细胞集落刺激因子自身抗体在中枢神经系统受累的诺卡氏杆菌病中的致病作用

IF 7.2 2区 医学 Q1 IMMUNOLOGY
Yu-Fang Lo, Shang-Yu Wang, Yi-Hui Wu, Mao-Wang Ho, Chun-Fu Yeh, Tsai-Yi Wu, Jhan-Jie Peng, You-Ning Lin, Jing-Ya Ding, Han-Po Shih, Chia-Chi Lo, Yu-Pei Chan, Cheng-Shyuan Rau, Chen-Yen Kuo, Kun-Hua Tu, Wei-Te Lei, Yi-Chun Chen, Cheng-Lung Ku
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引用次数: 0

摘要

目的:抗粒细胞-巨噬细胞集落刺激因子自身抗体(抗GM-CSF抗体)与加特隐球菌(C. gattii)感染和肺泡蛋白沉着病(PAP)的发病机制有关。在诺卡氏杆菌病病例中也发现了抗 M-CSF 蛋白,尤其是那些有播散性疾病的病例。本研究描述了一个病例系列,描述了诺卡地病患者抗 GM-CSF 抗体的临床特征和特异性:本研究招募了八名患者,以确定是否存在抗 GM-CSF 抗体。除了详细描述临床病程外,我们还利用患者的血浆样本对自身抗体的特征、异型、亚类、滴度和中和能力进行了深入研究:结果:在八名患者中,五人的抗 GM-CSF 抗体检测呈阳性,均累及中枢神经系统(CNS);而这些抗体呈阴性的患者均未发展为中枢神经系统念珠菌病。与之前记录的病例不同的是,我们的抗 GM-CSF 抗体患者均未表现出 PAP 症状。我们队列中抗 GM-CSF 抗体的滴度和中和活性与 C. gattii 隐球菌病和 PAP 患者中发现的抗 GM-CSF 抗体的滴度和中和活性没有明显差异。与众不同的是,有一名患者(患者 3)的抗 GM-CSF 抗体滴度和中和活性极低,与疾病严重程度无关。此外,在所有接受调查的中枢神经系统念珠菌病病例中都明显存在 IgM 自身抗体:结论:抗 GM-CSF 抗体的存在表明,中枢神经系统念珠菌病易感人群存在内在的免疫缺陷。即使自身抗体滴度较低,抗 GM-CSF 抗体的存在也有助于阐明中枢神经系统念珠菌病的易感性。因此,系统筛查抗 GM-CSF 抗体应被视为诺卡地病患者的重要诊断步骤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Pathogenic Role of Anti-Granulocyte-Macrophage Colony-Stimulating Factor Autoantibodies in the Nocardiosis with the Central Nervous System Involvement.

The Pathogenic Role of Anti-Granulocyte-Macrophage Colony-Stimulating Factor Autoantibodies in the Nocardiosis with the Central Nervous System Involvement.

Purpose: Anti-granulocyte-macrophage colony-stimulating factor autoantibodies (anti-GM-CSF Abs) are implicated in the pathogenesis of Cryptococcus gattii (C. gattii) infection and pulmonary alveolar proteinosis (PAP). Their presence has also been noted in nocardiosis cases, particularly those with disseminated disease. This study delineates a case series characterizing clinical features and specificity of anti-GM-CSF Abs in nocardiosis patients.

Methods: In this study, eight patients were recruited to determine the presence or absence of anti-GM-CSF Abs. In addition to the detailed description of the clinical course, we thoroughly investigated the autoantibodies regarding the characteristics, isotypes, subclasses, titers, and neutralizing capacities by utilizing the plasma samples from patients.

Results: Of eight patients, five tested positive for anti-GM-CSF Abs, all with central nervous system (CNS) involvement; patients negative for these antibodies did not develop CNS nocardiosis. Distinct from previously documented cases, none of our patients with anti-GM-CSF Abs exhibited PAP symptoms. The titer and neutralizing activity of anti-GM-CSF Abs in our cohort did not significantly deviate from those found in C. gattii cryptococcosis and PAP patients. Uniquely, one individual (Patient 3) showed a minimal titer and neutralizing action of anti-GM-CSF Abs, with no relation to disease severity. Moreover, IgM autoantibodies were notably present in all CNS nocardiosis cases investigated.

Conclusion: The presence of anti-GM-CSF Abs suggests an intrinsic immunodeficiency predisposing individuals toward CNS nocardiosis. The presence of anti-GM-CSF Abs helps to elucidate vulnerability to CNS nocardiosis, even with low titer of autoantibodies. Consequently, systematic screening for anti-GM-CSF Abs should be considered a crucial diagnostic step for nocardiosis patients.

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来源期刊
CiteScore
12.20
自引率
9.90%
发文量
218
审稿时长
2 months
期刊介绍: The Journal of Clinical Immunology publishes impactful papers in the realm of human immunology, delving into the diagnosis, pathogenesis, prognosis, or treatment of human diseases. The journal places particular emphasis on primary immunodeficiencies and related diseases, encompassing inborn errors of immunity in a broad sense, their underlying genotypes, and diverse phenotypes. These phenotypes include infection, malignancy, allergy, auto-inflammation, and autoimmunity. We welcome a broad spectrum of studies in this domain, spanning genetic discovery, clinical description, immunologic assessment, diagnostic approaches, prognosis evaluation, and treatment interventions. Case reports are considered if they are genuinely original and accompanied by a concise review of the relevant medical literature, illustrating how the novel case study advances the field. The instructions to authors provide detailed guidance on the four categories of papers accepted by the journal.
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