How I treat sickle cell disease with hematopoietic cell transplantation | Blood | American Society of Hematology
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Key PointsThe major cause of death in patients with ataxia-telangiectasia and hematological malignancies is treatment-related toxicity.The germ line ATM pa
Key PointsTransient TCD extends the window of opportunity for donor–specific central tolerance induction in mice.Transient TCD allows for allogeneic engraf
Key PointsUBA1 mutations were identified in 1% of patients with MDS and 7% of patients lacking myeloid mutations or established disease classification.Infl
A 52-year-old woman was admitted for unexplained thrombocytopenia with a 1-month history of nausea and anorexia. Initial blood tests showed leukocytes at 4.66 × 10…
Combining circulating absolute monocyte count and a 4-gene monocyte signature at leukapheresis predicts PFS of LBCL receiving CAR T cells.Monocytes depleti
The advent of reduced-intensity conditioning regimens, improvements in graft-versus-host disease prophylaxis, and better supportive care have permitted inc
Key PointsAllogeneic hematopoietic cell transplant recipients are at risk of clinically significant viral infections due to lack of T-cell immunity.The mul
Key PointsThe safety and efficacy benefits of ide-cel were proportionate in young and older patients despite frailty and geriatric characteristics.Treatmen
In this issue of Blood, Frigault et al1 describe the first-in-human trial of anti-CD37 chimeric antigen receptor (CAR) T cells in patients with refractory
Blood | 144 | 11 | September 2024