CRISPR/Cas-based gene editing in therapeutic strategies for beta-thalassemia.

IF 3.8 2区 生物学 Q2 GENETICS & HEREDITY
Human Genetics Pub Date : 2023-12-01 Epub Date: 2023-10-25 DOI:10.1007/s00439-023-02610-9
Shujun Zeng, Shuangyin Lei, Chao Qu, Yue Wang, Shuzhi Teng, Ping Huang
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引用次数: 0

Abstract

Beta-thalassemia (β-thalassemia) is an autosomal recessive disorder caused by point mutations, insertions, and deletions in the HBB gene cluster, resulting in the underproduction of β-globin chains. The most severe type may demonstrate complications including massive hepatosplenomegaly, bone deformities, and severe growth retardation in children. Treatments for β-thalassemia include blood transfusion, splenectomy, and allogeneic hematopoietic stem cell transplantation (HSCT). However, long-term blood transfusions require regular iron removal therapy. For allogeneic HSCT, human lymphocyte antigen (HLA)-matched donors are rarely available, and acute graft-versus-host disease (GVHD) may occur after the transplantation. Thus, these conventional treatments are facing significant challenges. In recent years, with the advent and advancement of CRISPR (clustered regularly interspaced short palindromic repeats)/Cas9 (CRISPR-associated protein 9) gene editing technology, precise genome editing has achieved encouraging successes in basic and clinical studies for treating various genetic disorders, including β-thalassemia. Target gene-edited autogeneic HSCT helps patients avoid graft rejection and GVHD, making it a promising curative therapy for transfusion-dependent β-thalassemia (TDT). In this review, we introduce the development and mechanisms of CRISPR/Cas9. Recent advances on feasible strategies of CRISPR/Cas9 targeting three globin genes (HBB, HBG, and HBA) and targeting cell selections for β-thalassemia therapy are highlighted. Current CRISPR-based clinical trials in the treatment of β-thalassemia are summarized, which are focused on γ-globin reactivation and fetal hemoglobin reproduction in hematopoietic stem cells. Lastly, the applications of other promising CRISPR-based technologies, such as base editing and prime editing, in treating β-thalassemia and the limitations of the CRISPR/Cas system in therapeutic applications are discussed.

Abstract Image

基于CRISPR/ cas的基因编辑在-地中海贫血治疗策略中的应用
β-地中海贫血是一种常染色体隐性遗传疾病,由HBB基因簇的点突变、插入和缺失引起,导致β-珠蛋白链产生不足。最严重的类型可能会出现并发症,包括儿童的巨大肝脾肿大、骨畸形和严重生长迟缓。β地中海贫血的治疗包括输血、脾切除和异基因造血干细胞移植(HSCT)。然而,长期输血需要定期进行除铁治疗。对于异基因造血干细胞移植,很少有人淋巴细胞抗原(HLA)匹配的供体,移植后可能发生急性移植物抗宿主病(GVHD)。因此,这些传统治疗方法面临着重大挑战。近年来,随着CRISPR(聚集性规则间隔短回文重复序列)/Cas9(CRISPR相关蛋白9)基因编辑技术的出现和进步,精确的基因组编辑在治疗包括β地中海贫血在内的各种遗传疾病的基础和临床研究中取得了令人鼓舞的成功。靶基因编辑的自体造血干细胞移植有助于患者避免移植物排斥反应和移植物抗宿主病,使其成为输血依赖性β-地中海贫血(TDT)的一种有前景的治疗方法。在这篇综述中,我们介绍了CRISPR/Cas9的发展和机制。重点介绍了CRISPR/Cas9靶向三个珠蛋白基因(HBB、HBG和HBA)和靶向细胞选择用于β地中海贫血治疗的可行策略的最新进展。综述了目前基于CRISPR的治疗β-地中海贫血的临床试验,重点是γ-珠蛋白的再激活和造血干细胞中胎儿血红蛋白的繁殖。最后,讨论了其他有前景的基于CRISPR的技术,如碱基编辑和引物编辑,在治疗β-地中海贫血中的应用,以及CRISPR/Cas系统在治疗应用中的局限性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Human Genetics
Human Genetics 生物-遗传学
CiteScore
10.80
自引率
3.80%
发文量
94
审稿时长
1 months
期刊介绍: Human Genetics is a monthly journal publishing original and timely articles on all aspects of human genetics. The Journal particularly welcomes articles in the areas of Behavioral genetics, Bioinformatics, Cancer genetics and genomics, Cytogenetics, Developmental genetics, Disease association studies, Dysmorphology, ELSI (ethical, legal and social issues), Evolutionary genetics, Gene expression, Gene structure and organization, Genetics of complex diseases and epistatic interactions, Genetic epidemiology, Genome biology, Genome structure and organization, Genotype-phenotype relationships, Human Genomics, Immunogenetics and genomics, Linkage analysis and genetic mapping, Methods in Statistical Genetics, Molecular diagnostics, Mutation detection and analysis, Neurogenetics, Physical mapping and Population Genetics. Articles reporting animal models relevant to human biology or disease are also welcome. Preference will be given to those articles which address clinically relevant questions or which provide new insights into human biology. Unless reporting entirely novel and unusual aspects of a topic, clinical case reports, cytogenetic case reports, papers on descriptive population genetics, articles dealing with the frequency of polymorphisms or additional mutations within genes in which numerous lesions have already been described, and papers that report meta-analyses of previously published datasets will normally not be accepted. The Journal typically will not consider for publication manuscripts that report merely the isolation, map position, structure, and tissue expression profile of a gene of unknown function unless the gene is of particular interest or is a candidate gene involved in a human trait or disorder.
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