Tag results:
hematopoietic stem cells
Immune Regulation News
Alloantigen-Activated (AAA) CD4+ T Cells Reinvigorate Host Endogenous T Cell Immunity to Eliminate Pre-established Tumors in Mice
[Journal of Experimental & Clinical Cancer Research] Alloantigen-activated CD4+ T cells were generated from CD4+ T cells isolated from BALB/c mice in cultures with dendritic cells induced from C57BL/6 mice.
Hematopoiesis News
p300 Suppresses the Transition of Myelodysplastic Syndromes to Acute Myeloid Leukemia
[JCI Insight] Scientists identified a tumor suppressor role of the acetyltransferase p300 in clinically relevant myelodysplastic syndromes models driven by mutations in the epigenetic regulators TET2, ASXL1, and SRSF2.
Hematopoiesis News
The Immune Landscape in BCR-ABL Negative Myeloproliferative Neoplasms: Inflammation, Infections and Opportunities for Immunotherapy
[British Journal of Haematology] Scientists focus on the immune landscape in patients with myeloproliferative neoplasms – the role of inflammation in disease pathogenesis, susceptibility to infection and emerging strategies for therapeutic immune modulation.
Hematopoiesis News
The Spliceosome Factor sart3 Regulates Hematopoietic Stem/Progenitor Cell Development in Zebrafish through the p53 Pathway
[Cell Death & Disease] Investigators characterized a zebrafish smu471 mutant with hematopoietic stem/progenitor cell defects and found that sart3 was the causative gene.
Hematopoiesis News
Stress Hematopoiesis Induces a Proliferative Advantage in TET2 Deficiency
[Leukemia] The authors developed a zebrafish tet2 mutant through which they showed that tet2 loss led to restricted hematopoietic differentiation combined with a modest upregulation of p53, which was also characteristic of many inherited bone marrow failure syndromes.
Hematopoiesis News
PD-1 Inhibition in Advanced Myeloproliferative Neoplasms
[Blood Advances] Investigators conducted a multicenter, open-label, Phase II, single-arm study of pembrolizumab in patients with DIPSS intermediate 2 or greater primary, post-essential thrombocythemia or post-polycythemia vera myelofibrosis that were ineligible for or were previously treated with ruxolitinib.