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依洛尤单抗治疗家族性高胆固醇血症的临床疗效和安全性:真实世界研究的系统评价和荟萃分析

Development of elexacaftor - tezacaftor - ivacaftor: Highly effective CFTR modulation for the majority of people with Cystic Fibrosis.

机构信息

Cystic Fibrosis Unit, Ludwig Engel Centre for Respiratory Research, Westmead Millennium Institute, University of Sydney at Westmead, Westmead, Australia.

National Jewish Health, Pulmonary, Internal Medicine and Pediatrics, Denver, CO, USA.

出版信息

Expert Rev Respir Med. 2021 Jun;15(6):723-735. doi: 10.1080/17476348.2021.1855980. Epub 2021 Feb 17.

Abstract

: Cystic fibrosis (CF), the most common life-shortening inherited disorder in people of European descent, also occurs in other ethnicities. The identification of the disease, the isolation of the causative gene, termed the cystic fibrosis transmembrane conductance regulator () and the improved survival from comprehensive multidisciplinary treatment is one of the success stories of modern medicine. Survival has increased dramatically over the last 50 years, from 10 years in the 1960s to 30 years in the 1990s and approximately 50 years currently.: This review will examine the development of highly effective modulators for CF which will revolutionize therapy for more than 90% of the people with CF. This review summarizes the development of triple combination CFTR modulator elexacaftor-tezacaftor-ivacaftor.: The development of this highly effective CFTR modulator for the majority of people with CF will likely change the landscape of CF care. The challenge is to now find highly effective therapy for the remaining 10% of the people with CF who may need other therapeutic agents to correct their primary defect.

摘要

囊性纤维化(CF)是欧洲裔人群中最常见的缩短寿命的遗传性疾病,也发生在其他种族中。该疾病的鉴定、致病基因的分离,即囊性纤维化跨膜电导调节剂(CFTR),以及综合多学科治疗的生存率提高,是现代医学的成功案例之一。过去 50 年来,生存率有了显著提高,从 20 世纪 60 年代的 10 年提高到 20 世纪 90 年代的 30 年,目前约为 50 年。本文将回顾高效 CFTR 调节剂的发展,这将彻底改变超过 90%的 CF 患者的治疗方法。本文总结了三联 CFTR 调节剂 elexacaftor-tezacaftor-ivacaftor 的发展。这种高效 CFTR 调节剂的开发可能会改变 CF 治疗的格局。挑战在于现在为剩余的 10%可能需要其他治疗药物来纠正其主要缺陷的 CF 患者找到高度有效的治疗方法。

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