METHOD FOR CONSTRUCTING CONGENITAL IMMUNODEFICIENCY GENE THERAPY VECTOR AND USE THEREOF
Disclosed are a recombinant lentiviral vector expressing the IL2RG gene, and the preparation thereof, wherein the vector is a self-inactivated third-generation lentiviral vector SIN, and the sequence of the IL2RG gene is as shown in SEQ ID NO: 1. Provided are a method for preparing the vector and th...
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Main Authors | , |
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Format | Patent |
Language | Chinese English French |
Published |
22.03.2018
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Subjects | |
Online Access | Get full text |
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Summary: | Disclosed are a recombinant lentiviral vector expressing the IL2RG gene, and the preparation thereof, wherein the vector is a self-inactivated third-generation lentiviral vector SIN, and the sequence of the IL2RG gene is as shown in SEQ ID NO: 1. Provided are a method for preparing the vector and the use of the vector in the preparation of a drug for treating primary immunodeficiency diseases.
L'invention concerne un vecteur lentiviral recombinant exprimant le gène IL2RG et la préparation associée, le vecteur étant un vecteur lentiviral auto-inactivant de type SIN de troisième génération, la séquence du gène IL2RG étant telle que représentée dans la SEQ ID NO : 1. L'invention concerne une méthode de préparation du vecteur et l'utilisation du vecteur dans la préparation d'un médicament servant au traitement de maladies de type immunodéficience primaire.
一种表达IL2RG基因的重组慢病毒载体及其制备。其中,该载体是自身失活的第三代慢病毒载体SIN,所述的IL2RG基因的序列如SEQ ID NO:1所示。提供了该载体的制备方法,以及该载体在制备治疗原发性免疫缺陷病药物中的用途。 |
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Bibliography: | Application Number: WO2017CN99603 |