Laboratory of Human Immunology and Infectious Diseases, Graduate Institute of Clinical Medical Sciences, Chang Gung University, No. 259, Wenhua 1st Rd., Guishan Dist, Taoyuan City, 33302, Taiwan.
Division of General Surgery, Department of Surgery, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
J Clin Immunol. 2024 Aug 12;44(8):176. doi: 10.1007/s10875-024-01775-w.
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.
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.
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.
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.
抗粒细胞-巨噬细胞集落刺激因子自身抗体(抗 GM-CSF Abs)与新型隐球菌(C. gattii)感染和肺泡蛋白沉积症(PAP)的发病机制有关。它们也存在于奴卡氏菌病病例中,特别是那些播散性疾病的病例。本研究描述了一系列病例,其特征是奴卡氏菌病患者抗 GM-CSF Abs 的临床特征和特异性。
本研究招募了 8 名患者以确定是否存在抗 GM-CSF Abs。除了详细描述临床过程外,我们还通过利用患者的血浆样本,彻底研究了这些自身抗体的特征、同种型、亚类、滴度和中和能力。
在 8 名患者中,有 5 名抗 GM-CSF Abs 检测阳性,均有中枢神经系统(CNS)受累;这些抗体阴性的患者未出现 CNS 奴卡氏菌病。与以前记录的病例不同,我们的抗 GM-CSF Abs 患者均无 PAP 症状。我们队列中的抗 GM-CSF Abs 的滴度和中和活性与新型隐球菌 cryptococcosis 和 PAP 患者没有显著差异。独特的是,一个人(患者 3)表现出抗 GM-CSF Abs 的最小滴度和中和作用,与疾病严重程度无关。此外,所有调查的 CNS 奴卡氏菌病病例均明显存在 IgM 自身抗体。
抗 GM-CSF Abs 的存在表明存在固有免疫缺陷,使个体易患 CNS 奴卡氏菌病。抗 GM-CSF Abs 的存在有助于阐明对 CNS 奴卡氏菌病的易感性,即使自身抗体的滴度较低。因此,系统筛查抗 GM-CSF Abs 应被视为奴卡氏菌病患者的重要诊断步骤。