RNA 干扰与神经肌肉疾病:聚焦遗传性转甲状腺素淀粉样变性。

IF 3.8 4区 医学 Q2 GENETICS & HEREDITY Current gene therapy Pub Date : 2024-01-01 DOI:10.2174/1566523223666230913110011
Marco Ceccanti, Maurizio Inghilleri
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引用次数: 0

摘要

神经肌肉疾病是影响周围神经系统的严重疾病,通常会在有限的时间内导致死亡。通过 RNA 干扰技术,许多新药正在彻底改变这些患者的预后和生活质量。然而,随着预期寿命的延长,一些新的问题和表型也会随之出现。在转甲状腺素介导的遗传性淀粉样变性病(ATTR-v,"v "代表 "变异")中,RNA 干扰被证明能有效减少肝脏合成转甲状腺素,但多发性神经病和心肌病的病情进展却显著增加。预期寿命的延长可能会导致肝外转甲状腺素沉积的器官(如大脑和眼睛)受累,而现有的治疗方法可能并不针对这些器官。本社论将讨论所有这些问题。
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RNA Interference and Neuromuscular Diseases: A Focus on Hereditary Transthyretin Amyloidosis.

Neuromuscular diseases are severe disorders affecting the peripheral nervous system, usually driving to death in a limited time. Many new drugs, through RNA-interference technology, are revolutionizing the prognosis and quality of life for these patients. Nevertheless, given the increased life expectancy, some new issues and phenotypes are expected to be revealed. In the transthyretin-mediated hereditary amyloidosis (ATTR-v, "v" for "variant"), the RNA interference was demonstrated to effectively reduce the hepatic synthesis of transthyretin, with a significant increase in disease progression in terms of polyneuropathy and cardiomyopathy. The increased life expectancy could promote the involvement of organs where the extra-hepatic transthyretin is deposited, such as the brain and eye, which are probably not targeted by the available treatments. All these issues are discussed in this editorial.

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来源期刊
Current gene therapy
Current gene therapy 医学-遗传学
CiteScore
6.70
自引率
2.80%
发文量
46
期刊介绍: Current Gene Therapy is a bi-monthly peer-reviewed journal aimed at academic and industrial scientists with an interest in major topics concerning basic research and clinical applications of gene and cell therapy of diseases. Cell therapy manuscripts can also include application in diseases when cells have been genetically modified. Current Gene Therapy publishes full-length/mini reviews and original research on the latest developments in gene transfer and gene expression analysis, vector development, cellular genetic engineering, animal models and human clinical applications of gene and cell therapy for the treatment of diseases. Current Gene Therapy publishes reviews and original research containing experimental data on gene and cell therapy. The journal also includes manuscripts on technological advances, ethical and regulatory considerations of gene and cell therapy. Reviews should provide the reader with a comprehensive assessment of any area of experimental biology applied to molecular medicine that is not only of significance within a particular field of gene therapy and cell therapy but also of interest to investigators in other fields. Authors are encouraged to provide their own assessment and vision for future advances. Reviews are also welcome on late breaking discoveries on which substantial literature has not yet been amassed. Such reviews provide a forum for sharply focused topics of recent experimental investigations in gene therapy primarily to make these results accessible to both clinical and basic researchers. Manuscripts containing experimental data should be original data, not previously published.
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