Department of Microbiology and Immunology, KUL - University of Leuven, Leuven, Belgium; VIB Center for Brain and Disease Research, Leuven, Belgium; University Hospitals Leuven, Leuven, Belgium.
Department of Microbiology and Immunology, KUL - University of Leuven, Leuven, Belgium; VIB Center for Brain and Disease Research, Leuven, Belgium.
J Allergy Clin Immunol. 2018 Aug;142(2):699-702.e12. doi: 10.1016/j.jaci.2018.04.008. Epub 2018 Apr 27.
IKAROS (encoded by is an important hematopoietic transcription factor critical for early B cell differentiation, with major defects known to lead to low B cell numbers and hypogammaglobulinemia. More perplexing is the link between variants and autoimmunity, including polymorphisms associated with susceptibility to SLE, and recently, rare variants driving monogenic autoimmunity. We identified a novel p.L188V mutation in in the index patient and her father and found this mutation to lead to loss of DNA binding. Peripheral B cells lacking a full complement of IKAROS function show upregulation of molecules accentuating B cell activation, while CD22, a key negative feedback circuit, is suppressed. The resulting hyperresponsiveness of peripheral B cells, in combination with elevated follicular helper T cell (Tfh) numbers, provides a putative mechanistic explanation for the association of variants with the emergence of autoimmune manifestations in this kindred.
IKAROS(由编码,是一种重要的造血转录因子,对早期 B 细胞分化至关重要,已知其主要缺陷会导致 B 细胞数量减少和低丙种球蛋白血症。更令人费解的是与自身免疫之间的联系,包括与 SLE 易感性相关的多态性,以及最近罕见变体驱动的单基因自身免疫。我们在索引患者及其父亲中鉴定出 IKAROS 中的新型 p.L188V 突变,并发现该突变导致 DNA 结合丧失。缺乏完整 IKAROS 功能的外周 B 细胞显示出增强 B 细胞激活的分子的上调,而 CD22,一个关键的负反馈回路,被抑制。外周 B 细胞的这种高反应性,结合滤泡辅助 T 细胞(Tfh)数量的升高,为该家族中与自身免疫表现相关的 IKAROS 变体提供了一个可能的机制解释。