Gene Therapy Options as New Treatment for Inherited Peripheral Neuropathy

  • Thenmozhi, Rajarathinam; 
  • Lee, Ji-Su; 
  • Park, Na Young; 
  • Choi, Byung-Ok; 
  • Hong, Young Bin
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초록

Inherited peripheral neuropathy (IPN) is caused by heterogeneous genetic mutations in more than 100 genes. So far, several treatment options for IPN have been developed and clinically evaluated using small molecules. However, gene therapy-based therapeutic strategies have not been aggressively investigated, likely due to the complexities of inheritance in IPN. Indeed, because the majority of the causative mutations of IPN lead to gain-of-function rather than loss-of-function, developing a therapeutic strategy is more difficult, especially considering gene therapy for genetic diseases began with the simple idea of replacing a defective gene with a functional copy. Recent advances in gene manipulation technology have brought novel approaches to gene therapy and its clinical application for IPN treatment For example, in addition to the classically used gene replacement for mutant genes in recessively inherited IPN, other techniques including gene addition to modify the disease phenotype, modulations of target gene expression, and techniques to edit mutant genes have been developed and evaluated as potent therapeutic strategies for dominantly inherited IPN. In this review, the current status of gene therapy for IPN and future perspectives will be discussed.

키워드

Inherited peripheral neuropathy; Gene therapy; Antisense oligonucleotide; miRNA; Gene editing; ASCORBIC-ACID TREATMENT; DISEASE TYPE 1A; SCHWANN-CELLS; MOUSE MODEL; ANTISENSE OLIGONUCLEOTIDES; HDAC6 INHIBITORS; HEREDITARY MOTOR; AXONAL LOSS; OPEN-LABEL; NERVE
제목
Gene Therapy Options as New Treatment for Inherited Peripheral Neuropathy
저자
Thenmozhi, Rajarathinam; Lee, Ji-Su; Park, Na Young; Choi, Byung-Ok; Hong, Young Bin
DOI
10.5607/en20004
발행일
2020-06
유형
Review
저널명
Experimental Neurobiology
권
29
호
3
페이지
177 ~ 188