AI Article Synopsis

  • IKAROS is a crucial transcription factor for early B cell development, and defects can cause low B cell levels and immune issues.
  • Recent findings connect IKAROS variants to autoimmune diseases, including Systemic Lupus Erythematosus (SLE), and specific mutations like p.L188V lead to loss of its DNA-binding ability.
  • B cells lacking IKAROS function are more activated and can negatively affect immune regulation, which, alongside increased follicular helper T cells, may explain the link between IKAROS mutations and autoimmunity in certain families.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541477PMC
http://dx.doi.org/10.1016/j.jaci.2018.04.008DOI Listing

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