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hematopoietic stem cells

Cytokine Autoantibodies Are Stable throughout the Hematopoietic Stem Cell Transplantation Course and Are Associated with Distinct Biomarker and Blood Cell Profiles

[Scientific Reports] Scientists found that cytokine-specific autoantibodies (c-aAb) levels were stable over the course of hematopoietic stem cell transplantation, including at high titres, with few individuals seeming to acquire high-titre levels of c-aAbs.

CoImmune Announces Positive Results from Phase I/II Clinical Trial of Allogeneic CAR-CIK Cells in Pediatric and Adult Patients with Acute Lymphoblastic Leukemia

[CoImmune, Inc.] CoImmune, Inc. announced that results from a Phase I/II clinical trial evaluating CARCIK-CD19, an investigational treatment based on the company’s chimeric antigen receptor modified cytokine induced killer cell platform, demonstrated sustained responses in pediatric and adult patients with B-cell acute lymphoblastic leukemia who had relapsed after allogeneic hematopoietic stem cell transplantation.

CD244 Expression Represents Functional Decline of Murine Hematopoietic Stem Cells after In Vitro Culture

[iScience] The authors showed that cultured HSCs expressed mast cell-related genes including Cd244 and suggested CD244 was a potent marker to exclude non-functional HSCs after in vitro culture thereby useful to elucidate mechanism of functional decline of HSCs during ex vivo treatment.

The Distinct Effects of P18 Overexpression on Different Stages of Hematopoiesis Involve TGF-β and Nf-κB Signaling

[Scientific Reports] Researchers established inducible P18/hESC lines and monitored the effects of P18 overexpression on hematopoietic differentiation and found evidence that P18 promoted hematopoiesis, a rare property among cyclin-dependent kinase inhibitors.

Conditionally Pathogenic Genetic Variants of a Hematopoietic Disease–Suppressing Enhancer

[Science Advances] Scientists described conditionally pathogenic enhancer motif variants that differentially affected hematopoietic development and regeneration. Despite normal developmental hematopoiesis, regeneration in response to chemotherapy, inflammation, and a therapeutic HSC mobilizer was compromised.

The Onset of Circulation Triggers a Metabolic Switch Required for Endothelial to Hematopoietic Transition

[Cell Reports] Investigators showed that in Ncx1−/− mouse embryos devoid of circulation, the HSC lineage developed until the phenotypic pro-HSC stage. Experimental activation of glycolysis resulted in decreased intraembryonic hematopoiesis, suggesting that the onset of circulation triggered metabolic changes that allowed HSC generation to proceed.

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