Department of Pediatrics, Division of Rheumatology/Immunology, Washington University in St. Louis, St. Louis, MO 63110, USA.
Department of Pediatrics, Division of Rheumatology/Immunology, Washington University in St. Louis, St. Louis, MO 63110, USA.
Semin Immunol. 2023 May;67:101761. doi: 10.1016/j.smim.2023.101761. Epub 2023 Apr 14.
Inborn errors of immunity (IEI) are a diverse group of monogenic disorders of the immune system due to germline variants in genes important for the immune response. Over the past decade there has been increasing recognition that acquired somatic variants present in a subset of cells can also lead to immune disorders or 'phenocopies' of IEI. Discovery of somatic mosaicism causing IEI has largely arisen from investigation of seemingly sporadic cases of IEI with predominant symptoms of autoinflammation and/or autoimmunity in which germline disease-causing variants are not detected. Disease-causing somatic mosaicism has been identified in genes that also cause germline IEI, such as FAS, and in genes without significant corresponding germline disease, such as UBA1 and TLR8. There are challenges in detecting low-level somatic variants, and it is likely that the extent of the somatic mosaicism causing IEI is largely uncharted. Here we review the field of somatic mosaicism leading to IEI and discuss challenges and methods for somatic variant detection, including diagnostic approaches for molecular diagnoses of patients.
先天性免疫缺陷(IEI)是一组由于免疫系统中对免疫反应重要的基因的种系变异引起的单基因疾病。在过去的十年中,人们越来越认识到,在一部分细胞中出现的获得性体细胞变异也可能导致免疫紊乱或 IEI 的“表型模拟”。导致 IEI 的体细胞嵌合现象的发现主要源于对具有自身炎症和/或自身免疫为主的表现的看似散发性 IEI 病例的研究,而这些病例中并未检测到种系致病变异。在导致种系 IEI 的基因中,如 FAS,以及在没有明显相应种系疾病的基因中,如 UBA1 和 TLR8,已经发现了导致 IEI 的致病体细胞嵌合现象。检测低水平体细胞变异存在挑战,很可能导致 IEI 的体细胞嵌合程度在很大程度上尚未被发现。在这里,我们回顾了导致 IEI 的体细胞嵌合现象的领域,并讨论了体细胞变异检测的挑战和方法,包括对患者进行分子诊断的诊断方法。