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lymphocytes

Landscape of Surfaceome and Endocytome in Human Glioma Is Divergent and Depends on Cellular Spatial Organization

[Proceedings of the National Academy of Sciences of the United States of America] The authors developed a platform integrated with a newly curated tumor surfaceome classifier that allowed profiling of primary 3D cultures and intact patient glioma tumors with preserved tissue architecture.

Intellia Therapeutics Announces First Patient Dosed in Phase I/IIa Clinical Trial of NTLA-5001 for the Treatment of Acute Myeloid Leukemia

[Intellia Therapeutics, Inc.] Intellia Therapeutics, Inc. announced that the first patient has been dosed with NTLA-5001, the company’s ex vivo CRISPR/Cas9 genome editing candidate for the treatment of AML.

Hematopoietic Cell Transplantation Donor-Derived Memory-Like NK Cells Functionally Persist after Transfer into Patients with Leukemia

[Science Translational Medicine] Reduced-intensity conditioning for HLA-haploidentical hematopoietic cell transplantation was augmented with same-donor memory-like natural killer (NK) cells on day +7 and 3 weeks of N-803 to treat patients with relapsed/refractory AML in a clinical trial.

Clonal Hematopoiesis, Myeloid Disorders and BAX-Mutated Myelopoiesis in Patients Receiving Venetoclax for CLL

[Blood] As BCL2 was an important determinant of survival of both myeloid progenitor and B cells, researchers investigated whether clinical and molecular abnormalities arise in the myeloid compartment during long-term continuous venetoclax treatment of chronic lymphocytic leukemia in 89 patients.

Gilteritinib Enhances Graft-versus-Leukemia Effects against FLT3-ITD Mutant Leukemia after Allogeneic Hematopoietic Stem Cell Transplantation

[Bone Marrow Transplantation] Scientists investigated whether gilteritinib, a selective FLT3 inhibitor, could enhance graft-versus-leukemia effects against FLT3 internal tandem duplication mutant transfected Ba/F3 leukemia in mice.

Adoptive Transfer of Ex Vivo Expanded Regulatory T Cells Improves Immune Cell Engraftment and Therapy-Refractory Chronic GvHD

[Molecular Therapy] Investigators treated three children suffering from severe, therapy-refractory GvHD with polyclonally expanded regulatory T cells generated from the original stem cell donor.

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