Division of Clinical Immunology and Allergy, Department of Internal Medicine, University Hospital and Faculty of Medicine, Geneva, Switzerland.
Institute of Pharmacology, University of Bern, Bern, Switzerland.
Blood. 2019 Nov 28;134(22):1941-1950. doi: 10.1182/blood.2019001705.
Immune system failure in primary antibody deficiencies (PADs) has been linked to recurrent infections, autoimmunity, and cancer, yet clinical judgment is often based on the reactivity to a restricted panel of antigens. Previously, we demonstrated that the human repertoire of carbohydrate-specific immunoglobulin G (IgG) exhibits modular organization related to glycan epitope structure. The current study compares the glycan-specific IgG repertoires between different PAD entities. Distinct repertoire profiles with extensive qualitative glycan-recognition defects were observed, which are characterized by the common loss of Galα and GalNAc reactivity and disease-specific recognition of microbial antigens, self-antigens, and tumor-associated carbohydrate antigens. Antibody repertoire analysis may provide a useful tool to elucidate the degree and the clinical implications of immune system failure in individual patients.
原发性抗体缺陷症 (PAD) 患者的免疫系统功能障碍与反复感染、自身免疫和癌症有关,但临床判断往往基于对有限抗原谱的反应性。先前,我们证明了人类糖基特异性免疫球蛋白 G (IgG) 库与聚糖表位结构相关,表现出模块化组织。本研究比较了不同 PAD 实体的糖基特异性 IgG 库。观察到不同的库特征图谱,表现为广泛的定性糖识别缺陷,其特征是 Galα 和 GalNAc 反应性的常见丧失,以及微生物抗原、自身抗原和肿瘤相关碳水化合物抗原的疾病特异性识别。抗体库分析可能为阐明个体患者免疫系统功能障碍的程度和临床意义提供有用的工具。