| Literature DB >> 36138187 |
Matthew T Witkowski1,2, Soobeom Lee3,4, Eric Wang5,6, Anna K Lee3, Alexis Talbot7, Chao Ma8,9, Nikolaos Tsopoulidis10,11,12, Justin Brumbaugh13, Yaqi Zhao14, Kathryn G Roberts14, Simon J Hogg5, Sofia Nomikou3, Yohana E Ghebrechristos3, Palaniraja Thandapani3, Charles G Mullighan14, Konrad Hochedlinger10,11,12, Weiqiang Chen8,9, Omar Abdel-Wahab5,15, Justin Eyquem7,16,17,18, Iannis Aifantis19.
Abstract
B cell progenitor acute lymphoblastic leukemia (B-ALL) treatment has been revolutionized by T cell-based immunotherapies-including chimeric antigen receptor T cell therapy (CAR-T) and the bispecific T cell engager therapeutic, blinatumomab-targeting surface glycoprotein CD19. Unfortunately, many patients with B-ALL will fail immunotherapy due to 'antigen escape'-the loss or absence of leukemic CD19 targeted by anti-leukemic T cells. In the present study, we utilized a genome-wide CRISPR-Cas9 screening approach to identify modulators of CD19 abundance on human B-ALL blasts. These studies identified a critical role for the transcriptional activator ZNF143 in CD19 promoter activation. Conversely, the RNA-binding protein, NUDT21, limited expression of CD19 by regulating CD19 messenger RNA polyadenylation and stability. NUDT21 deletion in B-ALL cells increased the expression of CD19 and the sensitivity to CD19-specific CAR-T and blinatumomab. In human B-ALL patients treated with CAR-T and blinatumomab, upregulation of NUDT21 mRNA coincided with CD19 loss at disease relapse. Together, these studies identify new CD19 modulators in human B-ALL.Entities:
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Year: 2022 PMID: 36138187 DOI: 10.1038/s41590-022-01314-y
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 31.250