B cell focused transient immune suppression protocol for efficient AAV readministration to the liver-Reference-Cited by-同舟云学术

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B cell focused transient immune suppression protocol for efficient AAV readministration to the liver

Published:2024-03 Issue:1 Volume:32 Page:101216
ISSN:2329-0501
Container-title:Molecular Therapy - Methods & Clinical Development
language:en
Short-container-title:Molecular Therapy - Methods & Clinical Development

Author:

Rana Jyoti,Herzog Roland W.,Muñoz-Melero Maite,Yamada Kentaro,Kumar Sandeep R.P.,Lam Anh K.,Markusic David M.,Duan Dongsheng,Terhorst Cox,Byrne Barry J.,Corti Manuela,Biswas Moanaro^ORCID

Funder

NHLBI

NCI

NIAID

NIDDK

NIH

Publisher

Elsevier BV

Reference56 articles.

1. Fantastic AAV Gene Therapy Vectors and How to Find Them-Random Diversification, Rational Design and Machine Learning;Becker;Pathogens,2022

2. Characterization of a Bioengineered AAV3B Capsid Variant with Enhanced Hepatocyte Tropism and Immune Evasion;Rana;Hum. Gene Ther.,2023

3. Current Clinical Applications of In Vivo Gene Therapy with AAVs;Mendell;Mol. Ther.,2021

4. Two gene therapies for hemophilia available: Now what?;Pierce;Mol. Ther.,2023

5. First hemophilia B gene therapy approved: More than two decades in the making;Herzog;Mol. Ther.,2023

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Innate Immune Sensing of Adeno-Associated Virus Vectors;Human Gene Therapy;2024-07-01

2. Chopping down antibodies for a good cause;Molecular Therapy;2024-07

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