bioRxivCancer BiologyPreprint
Primary CD34+ cells of patients with VEXAS syndrome are highly sensitive to targeted treatment with TAK-243 and pevonedistat
Daniel NowakiD, Marie Demmerle, Alessa Klär, Alexander StreueriD, Vladimir RiaboviD, Eva AltrockiD, Felicitas RappiD, Ann‐Christin Belzer, Teresa Klink, Meret Hahn, Franziska Hofmann, Verena NowakiD, Nadine Weimer, Julia Obländer, Iris Palme, Melda Göl, Ali DarwichiD, Laurenz SteineriD, Mohammed L. AbbaiD, Georgia Metzgeroth, Wolf‐Karsten HofmanniD, Nanni SchmittiD
Abstract
Vacuoles, E1 enzyme, X-linked, Autoinflammatory, Somatic (VEXAS) syndrome is an autoinflammatory disease characterized by somatically acquired UBA1 mutations in hematopoietic stem cells. VEXAS patients present with significant therapeutic challenges such as severe treatment-resistant inflammation and predisposition to myeloid malignancies. In this study, we evaluated the efficacy of TAK-243, a UBA1 inhibitor, and pevonedistat, a NEDD8 inhibitor, in vitro on primary CD34+ hematopoietic stem and progenitor cells (HSPCs) from patients with VEXAS syndrome (n=5), myelodysplastic neoplasms (MDS) (n=10), as well as healthy controls (n=10). Our findings revealed that VEXAS patient-derived HSPCs exhibited significantly higher sensitivity to both TAK-243 (IC50: 22 nM) and pevonedistat (IC50: 553 nM) compared to MDS (IC50: 133 nM and 1048 nM, respectively) and healthy controls (IC50: 192 nM and 1107 nM, respectively) as demonstrated by reduced cell viability. Furthermore, VEXAS CD34+ cells exhibited significantly higher levels of apoptosis after treatment with both inhibitors. These results suggest that TAK-243 and pevonedistat selectively target UBA1-mutated progenitor cells, and indicate a broad therapeutic window in which malignant cells are eradicated but healthy hematopoiesis is not yet compromised. This study provides a strong rationale for further clinical investigation of TAK-243 and pevonedistat as targeted therapies for VEXAS patients, offering hope for improved management of this clinically challenging disorder and contributing to our understanding of its underlying molecular mechanisms.
- organism: human
- research focus: drug response / drug discovery
- research focus: cell type annotation
- research focus: differential expression
- research focus: cell-cell communication
- approach: experimental assay
- Citations
- 0
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Single-cell genotype-phenotype mapping identifies therapeutic vulnerabilities in VEXAS syndrome
Saravanan Ganesan, Rebecca M. Murray, … Dan Avi Landau·bioRxiv·May 19, 2024
- Disturbing immune homeostasis by neutrophil loss of Uba1 induces VEXAS-like autoinflammatory disease in mice
Ge Dong, Jingjing Liu, … Zhigang Cai·Journal of Clinical InvestigationPeer-reviewed·Sep 4, 2025
- Locus-specific transposable element expression drives human hematopoietic stem cell disease pathophysiology
Angelica Varesi, Sontago Dong, … John E. Dick·bioRxiv·Aug 5, 2026
- Characterization of a maintainable human myeloid model of VEXAS syndrome with enhanced TNF-induced cell death and DAMP release
Yuma Sakamoto, Nobuyasu Baba, … Tomoyuki Mukai·bioRxiv·Sep 14, 2026
- Cell autonomous inflammation in VEXAS is mediated by cGAS-STING
Samuel J. Magaziner, Jason C. Collins, … David B. Beck·bioRxiv·May 29, 2026
- UBA1 Mutations Drive RIPK1-Mediated Cell Death and Monocyte Dysfunction in VEXAS Syndrome
Paul Breillat, Samuel J. Magaziner, … Benjamin Terrier·bioRxiv·Oct 6, 2025