Clinical Trials and Research1 min read
Base Editing of HBG1 and HBG2 Promoters for Sickle Cell Disease
About this article
- Published
- Last updated
- Further reading
- Read More(opens in a new tab)

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).