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Part of Sickle Cell Disease on Somebody To Talk To

Clinical Trials and Research1 min read

Base Editing of HBG1 and HBG2 Promoters for Sickle Cell Disease

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The New England Journal of Medicine

Sickle cell disease is characterized by chronic hemolytic anemia and recurrent severe vaso-occlusive crises. Ristoglogene autogetemcel (risto-cel) includes autologous CD34+ hematopoietic stem and progenitor cells that have been base-edited to target the HBG1 and HBG2 promoters and inhibit BCL11A binding without altering BCL11A expression, yielding a switch in hemoglobin production from sickle hemoglobin (HbS) to antisickling fetal hemoglobin (HbF).

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