Gene Therapy for Primary Immunodeficiency

Over the past 3 decades, there has been significant progress in refining gene therapy technologies and procedures. Transduction of hematopoietic stem cells ex vivo using lentiviral vectors can now create a highly effective therapeutic product, capable of reconstituting many different immune system d...

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Bibliographic Details
Main Authors: Benjamin C. Houghton, Claire Booth
Format: Article
Language:English
Published: Wolters Kluwer 2021-01-01
Series:HemaSphere
Online Access:http://journals.lww.com/10.1097/HS9.0000000000000509