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镰状细胞病的治疗方法:异体和自体策略综述。

Curative approaches for sickle cell disease: A review of allogeneic and autologous strategies.

机构信息

Division of Hematology/Oncology, Boston Children's Hospital, Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, United States; Harvard Stem Cell Institute, Department of Pediatrics, Harvard Medical School, Boston, MA 02115, United States.

Gene Therapy Program, Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, MA 02115, United States.

出版信息

Blood Cells Mol Dis. 2017 Sep;67:155-168. doi: 10.1016/j.bcmd.2017.08.014. Epub 2017 Sep 1.

Abstract

Despite sickle cell disease (SCD) first being reported >100years ago and molecularly characterized >50years ago, patients continue to experience severe morbidity and early mortality. Although there have been substantial clinical advances with immunizations, penicillin prophylaxis, hydroxyurea treatment, and transfusion therapy, the only cure that can be offered is hematopoietic stem cell transplantation (HSCT). In this work, we summarize the various allogeneic curative approaches reported to date and discuss open and upcoming clinical research protocols. Then we consider gene therapy and gene editing strategies that may enable cure based on autologous HSCs.

摘要

尽管镰状细胞病(SCD)早在 100 多年前就有报道,50 多年前就有分子特征描述,但患者仍持续经历严重的发病率和早逝。尽管免疫接种、青霉素预防、羟基脲治疗和输血治疗取得了实质性的临床进展,但唯一可以提供的治愈方法是造血干细胞移植(HSCT)。在这项工作中,我们总结了迄今为止报道的各种同种异体治愈方法,并讨论了正在进行和即将进行的临床研究方案。然后我们考虑基因治疗和基因编辑策略,这些策略可能基于自体 HSCs 实现治愈。

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