| Vol. 13.45 – 15 November, 2022 |
| |
|
|
| Investigators discovered that myeloid-derived suppressor cells secreted itaconate that can be taken up by CD8+ T cells and suppressed their proliferation, cytokine production, and cytolytic activity. [Nature Metabolism] |
|
|
|
| PUBLICATIONSRanked by the impact factor of the journal |
|
|
|
| Scientists developed a proof of concept therapeutic base editing strategy to address two of the most prevalent FANCA mutations in patient hematopoietic stem and progenitor cells. [Nature Communications] |
|
|
|
| Researchers utilized base editing to generate a variety of mutations in the −200 region of the HBG promoters, including potent combinations of four to eight γ-globin-inducing mutations. [Nature Communications] |
|
|
|
| In taking a multi-omic approach, scientists demonstrated that CDK9 inhibition with VIP152 disrupted the highly ordered assembly of the transcriptional machinery, thereby promoting cellular stress and inevitable cell death. [Leukemia] |
|
|
|
| In diabetic mice, co-transplantation of donor-matched islets and hematopoietic cells durably corrected diabetes without chronic immunosuppression and no appreciable evidence of graft-versus-host disease. [Cell Reports] |
|
|
|
| Investigators used a mouse model of chronic multifocal osteomyelitis to assess the effects of a spontaneously developed inflammatory condition on HSCs. [EMBO Reports] |
| |
|
|
| Researchers studied the dynamics of memory T cells subpopulations and cytokines in the blood of allogeneic hematopoietic stem cell transplantation patients after mesenchymal stromal cell administration. [Transplantation and Cellular Therapy] |
|
|
|
|
A study by the Pediatric Diseases (PDWP) and Inborn Error Working Party (IEWP) of the European Society for Blood and Marrow Transplantation (EBMT) presented the response of 82 pediatric patients who developed transplantation-associated thrombotic microangiopathy and treated with eculizumab. [Bone Marrow Transplantation] |
| | Scientists identified 206 patients with mutated Nucleophosmin 1 (NPM1) and compared their outcomes to 1516 patients with NPM1 wild-type. It was found that NPM1 mutational status had minimal impact on prognosis in relapsed or refractory AML. [Blood Advances] |
|
|
|
|
| Investigators review the recent advances in the understanding of early events after the acquisition of a driver gene mutation that cause myeloproliferative neoplasms. [Blood] |
|
|
|
|
| SELLAS Life Sciences Group, Inc. announced important updates relating to its ongoing Phase III open-label registrational clinical trial for galinpepimut-S in AML patients who have achieved complete remission following second-line salvage therapy. [SELLAS Life Sciences Group, Inc.] |
|
|
|
| Aptose Biosciences, Inc. announced the dosing of the first patient to receive a continuous dosing regimen of the G3 formulation of luxeptinib, a potent, non-covalent oral inhibitor of BTK and FLT3, in the ongoing Phase Ia/b clinical trial in patients with relapsed or refractory AML. [Aptose Bioscience, Inc.] |
|
|
|
|
| December 6 – 10, 2022 San Antonio, Texas, United States |
|
|
|
|
|
| AstraZeneca – Waltham, Massachusetts, United States |
|
|
|
| Washington University School of Medicine – St. Louis, Missouri, United States |
|
|
|
| Johns Hopkins School of Medicine – Baltimore, Maryland, United States |
|
|
|
| German Cancer Research Center in the Helmholtz Association – Munich, Germany |
|
|
|
| STEMCELL Technologies, Inc. – Boston, Massachusetts, United States |
|
|
|
|