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Sakuma, Maki; Blombery, Piers; Meggendorfer, Manja; Haferlach, Claudia; Lindauer, Markus; Martens, Uwe M; Kern, Wolfgang; Haferlach, Torsten; Walter, Wencke
Leukemia, 05/2023, Volume: 37, Issue: 5Journal Article
UBA1 is an X-linked gene and encodes an ubiquitin-activating enzyme. Three somatic mutations altering the alternative start codon (M41) in UBA1 in hematopoietic precursor cells have recently been described, resulting in a syndrome of severe inflammation, cytopenias, and the presence of intracellular vacuoles in hematopoietic precursors - termed VEXAS syndrome, a predominantly male disease. Here we present a patient with clinical features of VEXAS who harbored two novel somatic variants in UBA1 (I894S and N606I). To better understand the clinical relevance and biological consequences of non-M41 (UBA1 ) variants, we analyzed the whole genome and transcriptome data of 4168 patients with hematological malignancies and detected an additional 16 UBA1 putative somatic variants with a clear sex-bias in patients with myeloid malignancies. Patients diagnosed with myeloid malignancies carrying UBA1 putative somatic variants either had vacuoles or immunodysregulatory symptoms. Analysis of the transcriptome confirmed neutrophil activation in VEXAS patients compared to healthy controls but did not result in a specific transcriptomic signature of UBA1 patients in comparison with MDS patients. In summary, we have described multiple putative novel UBA1 variants in patients with various hematological malignancies expanding the genomic spectrum of VEXAS syndrome.
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