Red Blood Cell Anchoring Enables Targeted Transduction and Re‐Administration of AAV‐Mediated Gene Therapy-Reference-Cited by-同舟云学术

Red Blood Cell Anchoring Enables Targeted Transduction and Re‐Administration of AAV‐Mediated Gene Therapy

Published:2022-07-03 Issue:24 Volume:9 Page:2201293
ISSN:2198-3844
Container-title:Advanced Science
language:en
Short-container-title:Advanced Science

Author:

Zhao Zongmin¹²,Kim Jayoung¹²,Suja Vinny Chandran¹²,Kapate Neha¹²³,Gao Yongsheng¹²,Guo Junling¹²,Muzykantov Vladimir R.⁴,Mitragotri Samir¹²^ORCID

Affiliation:

1. John A. Paulson School of Engineering and Applied Sciences Harvard University Cambridge MA 02138 USA

2. Wyss Institute for Biologically Inspired Engineering at Harvard University Boston MA 02115 USA

3. Harvard‐MIT Division of Health Sciences and Technology Massachusetts Institute of Technology Cambridge MA 02139 USA

4. Department of Systems Pharmacology and Translational Therapeutics and Center for Translational Targeted Therapeutics and Nanomedicine Perelman School of Medicine University of Pennsylvania Philadelphia PA 19104 USA

Publisher

Wiley

Subject

General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/advs.202201293

Reference41 articles.

1. Engineering adeno-associated virus vectors for gene therapy

2. Adeno-associated Virus (AAV) Serotypes Have Distinctive Interactions with Domains of the Cellular AAV Receptor

3. Adeno-associated virus vector as a platform for gene therapy delivery

4. Analysis of AAV Serotypes 1–9 Mediated Gene Expression and Tropism in Mice After Systemic Injection

5. Viral vector‐based gene therapies in the clinic

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