慢性肉芽肿性疾病
医学
NADPH氧化酶
髓系细胞
免疫学
外显子
髓样
基因组编辑
疾病
造血
遗传增强
免疫缺陷
基因
氧化酶试验
并发症
造血干细胞移植
不利影响
病理
作者
Jennifer L. Gori,Élie Haddad,Haydar Frangoul,Donald B. Kohn,Emma Morris,Bradley N. Martin,Briana Deary,Mike Nickerson,Rebecca L. Scholz,Isabel Fernández,Karine Léveillé,Suk See De Ravin,Elizabeth M. Kang,Marie Pierzynski,Tyra Estwick,Patricia Littel,Douglas B. Kuhns,Debra A. Long Priel,Pierre Teira,Stuart E. Turvey
标识
DOI:10.1056/nejmoa2509807
摘要
. We developed PM359, an autologous CD34+ hematopoietic stem-cell therapy in which prime editing is used to correct delGT. Two participants received PM359 after myeloid conditioning with busulfan: neutrophils and platelets engrafted promptly in both patients. Adverse events were consistent with myeloid conditioning with busulfan. NADPH oxidase activity was observed in neutrophils within 1 month and was maintained for 6 months and 4 months as of the last follow-up visit in Participants 1 and 2, respectively. These results support further investigation of prime editing of CD34+ cells to treat p47-CGD. (Funded by Prime Medicine; ClinicalTrials.gov number, NCT06559176.).
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