In-vivo-targeted gene delivery using adenovirus-antibody site-specific covalent conjugates

Safe and efficient nucleic acid delivery to targeted cell populations remains a challenge in the fields of cell and gene therapy. Toward this end, we attempted to utilize the "DogTag-DogCatcher" system to target adenoviral vectors. "DogTag" is a short peptide that forms a spontaneous isopeptide bond upon mixing with its partner protein, "DogCatcher." We genetically incorporated the DogTag peptide into the protein responsible for initial binding of the virus to its target cell, the fiber. This allowed permanent linking of DogCatcher-fused single-domain or single-chain antibodies at the fiber. This modification allowed simple, effective, and exclusive targeting of the vector to cells bound by the linked antibody. This enhanced gene transfer into primary B and T cells by up to 60-fold <i>in vitro</i> and 2- to 3-fold <i>in vivo</i> in mice without other alterations to vector tropism. Although the system's <i>in vivo</i> performance is currently suboptimal and additional engineering is needed prior to further use, these studies form the basis of a novel method for targeting adenovirus that can be combined with additional well-characterized adenovirus modifications toward applications in cell engineering, gene therapy, vaccines, oncolytics, and others.

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Publication Details

Journal
Molecular Therapy — Methods & Clinical Development
Published
2025-05-26
DOI
https://doi.org/10.1016/j.omtm.2025.101497
Citations
2
Primary Topic
Virus-based gene therapy research
Type
article
Field-Weighted Citation Impact
3.63

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article

In-vivo-targeted gene delivery using adenovirus-antibody site-specific covalent conjugates

Hongjie Guo, David T. Curiel, Zhi Hong Lu, Igor P. Dmitriev et al.
2 citations
Molecular Therapy — Methods & Clinical Development
Virus-based gene therapy research
3.63
article

In-vivo-targeted gene delivery using adenovirus-antibody site-specific covalent conjugates

Hongjie Guo, David T. Curiel, Zhi Hong Lu, Igor P. Dmitriev, Paul J. Rice-Boucher, Jacqueline M. Tremblay, Charles B. Shoemaker, Elena A. Kashentseva
article en
2 citations

Abstract

Safe and efficient nucleic acid delivery to targeted cell populations remains a challenge in the fields of cell and gene therapy. Toward this end, we attempted to utilize the "DogTag-DogCatcher" system to target adenoviral vectors. "DogTag" is a short peptide that forms a spontaneous isopeptide bond upon mixing with its partner protein, "DogCatcher." We genetically incorporated the DogTag peptide into the protein responsible for initial binding of the virus to its target cell, the fiber. This allowed permanent linking of DogCatcher-fused single-domain or single-chain antibodies at the fiber. This modification allowed simple, effective, and exclusive targeting of the vector to cells bound by the linked antibody. This enhanced gene transfer into primary B and T cells by up to 60-fold <i>in vitro</i> and 2- to 3-fold <i>in vivo</i> in mice without other alterations to vector tropism. Although the system's <i>in vivo</i> performance is currently suboptimal and additional engineering is needed prior to further use, these studies form the basis of a novel method for targeting adenovirus that can be combined with additional well-characterized adenovirus modifications toward applications in cell engineering, gene therapy, vaccines, oncolytics, and others.

Molecular Therapy — Methods & Clinical DevelopmentVol. 33(2)
Washington University in St. Louis (US), New England Disabled Sports (US), Tiger Optics (United States) (US)
National Heart, Lung, and Blood Institute, National Institute of Allergy and Infectious Diseases, National Institute of Biomedical Imaging and Bioengineering
Zero hunger
Openalex Percentile: Top 8%
Virus-based gene therapy research
3.63
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