AI Article Synopsis

  • - The study highlights the role of regulatory T (T) cells in preventing autoimmunity, with a focus on the impact of variants in the Pre-B cell leukemia transcription factor 1 (Pbx1) on lupus susceptibility.
  • - Overexpression of Pbx1 disrupts T cell homeostasis, leading to an increase in inflammatory CD4 T cells and a decrease in the stability and suppressive function of T cells, particularly in lupus-affected individuals.
  • - The research indicates that Pbx1 helps maintain T cell stability and normal cell cycle progression, which is crucial in preventing the expansion of inflammatory T cells that could worsen lupus symptoms.

Article Abstract

The maintenance of regulatory T (T) cells critically prevents autoimmunity. Pre-B cell leukemia transcription factor 1 () variants are associated with lupus susceptibility, particularly through the expression of a dominant negative isoform in CD4 T cells. overexpression impaired T cell homeostasis and promoted inflammatory CD4 T cells. Here, we showed a high expression of in human and murine T cells, which is decreased in lupus patients and mice. deficiency or overexpression reduced the number, stability, and suppressive activity of T cells, which increased murine responses to immunization and autoimmune induction. Mechanistically, deficiency altered the expression of genes implicated in cell cycle and apoptosis in T cells. Intriguingly, , a Rho-GTPase previously associated with T homeostasis, was directly transactivated by Pbx1. Our results suggest that the maintenance of T cell homeostasis and stability by through cell cycle progression prevent the expansion of inflammatory T cells that otherwise exacerbates lupus progression in the hosts.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10971436PMC
http://dx.doi.org/10.1126/sciadv.adi4310DOI Listing

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