Neutrophils take center stage in VEXAS syndrome pathogenesis

Vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic (VEXAS) syndrome is an adult-onset inflammatory disorder caused by somatic UBA1 mutations in hematopoietic stem cells. UBA1 encodes a key enzyme that catalyzes protein ubiquitination. Clinically, VEXAS is characterized by systemic inflammation and hematologic abnormalities. Patient studies have hinted that the transition of UBA1-mutated stem cells into proinflammatory myeloid precursors may propagate the manifestations of VEXAS syndrome. In this issue of the JCI, Dong and colleagues developed nine unique conditional knockout mouse strains and found that only neutrophil-specific Uba1 deletion reproduced VEXAS syndrome-like findings. The observed phenotype was at least in part due to inflammatory reprogramming and longer survival of the mutant neutrophils. In addition to deepening our mechanistic understanding of VEXAS syndrome pathogenesis, this work should provide a platform to pursue more targeted approaches to treatment.

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Publication Details

Journal
Journal of Clinical Investigation
Published
2025-11-02
DOI
https://doi.org/10.1172/jci199299
Primary Topic
Otitis Media and Relapsing Polychondritis
Type
article
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article

Neutrophils take center stage in VEXAS syndrome pathogenesis

Ajay Tambralli, Jason S. Knight
Journal of Clinical Investigation
Otitis Media and Relapsing Polychondritis
article

Neutrophils take center stage in VEXAS syndrome pathogenesis

Ajay Tambralli, Jason S. Knight
article en

Abstract

Vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic (VEXAS) syndrome is an adult-onset inflammatory disorder caused by somatic UBA1 mutations in hematopoietic stem cells. UBA1 encodes a key enzyme that catalyzes protein ubiquitination. Clinically, VEXAS is characterized by systemic inflammation and hematologic abnormalities. Patient studies have hinted that the transition of UBA1-mutated stem cells into proinflammatory myeloid precursors may propagate the manifestations of VEXAS syndrome. In this issue of the JCI, Dong and colleagues developed nine unique conditional knockout mouse strains and found that only neutrophil-specific Uba1 deletion reproduced VEXAS syndrome-like findings. The observed phenotype was at least in part due to inflammatory reprogramming and longer survival of the mutant neutrophils. In addition to deepening our mechanistic understanding of VEXAS syndrome pathogenesis, this work should provide a platform to pursue more targeted approaches to treatment.

Journal of Clinical InvestigationVol. 135(21)
University of Michigan (US), Center for Rheumatology (US)
Openalex Percentile: Top 54%
Otitis Media and Relapsing Polychondritis
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Neutrophils take center stage in VEXAS syndrome pathogenesis — Ajay Tambralli, Jason S. Knight · Journal of Clinical Investigation (2025) | TGRS Research Map | TGRS