Therapeutics: Gene Therapy For Alpha-1 Antitrypsin Deficiency

ALPHA-1 ANTITRYPSIN DEFICIENCY: METHODS AND PROTOCOLS(2017)

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摘要
This review seeks to give an overview of alpha-1 antitrypsin deficiency, including the different disease phenotypes that it encompasses. We then describe the different therapeutic endeavors that have been undertaken to address these different phenotypes. Lastly we discuss future potential therapeutics, such as genome editing, and how they may play a role in treating alpha-1 antitrypsin deficiency.
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关键词
SERPINA1, Emphysema, Liver disease, Genome editing, CRISPR/Cas9
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