Circumventing Antivector Immunity: Potential Use of Nonhuman Adenoviral Vectors
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Adenoviruses are efficient gene delivery vectors based on their ability to transduce a wide variety of cell types and drive high-level transient transgene expression. While there have been advances in modifying human adenoviral (HAdV) vectors to increase their safety profile, there are still pitfalls that need to be further addressed. Preexisting humoral and cellular immunity against common HAdV serotypes limits the efficacy of gene transfer and duration of transgene expression. As an alternative, nonhuman AdV (NHAdV) vectors can circumvent neutralizing antibodies against HAdVs in immunized mice and monkeys and in human sera, suggesting that NHAdV vectors could circumvent preexisting humoral immunity against HAdVs in a clinical setting. Consequently, there has been an increased interest in developing NHAdV vectors for gene delivery in humans. In this review, we outline the recent advances and limitations of HAdV vectors for gene therapy and describe examples of NHAdV vectors focusing on their immunogenicity, tropism, and potential as effective gene therapy vehicles.
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LNP-formulated mRNA can be used as a platform technology, which does not induce anti-vector immunity that can be observed with viral vectors such as adenoviruses.
“An important finding of our study is that LNP-formulated mRNA can be used as a platform technology, which does not induce anti-vector immunity that can be observed with viral vectors such as adenoviruses.29”
From Unmodified mRNA in LNPs constitutes a competitive technology for prophylactic vaccines (2017) · cites this paper as [29]
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- Authors
- Lopez-Gordo, E., Podgorski, I. I., Downes, N., & Alemany, R.
- Affiliations
- University of Glasgow
- HUN-REN Veterinary Medical Research Institute (HU)
- University of Eastern Finland (FI)
- Institut Català d'Oncologia
- Venue
- Human Gene Therapy
- Publisher
- SAGE Publications
- Published
- 2014-02-05
- Volume
- 25
- Issue
- 4
- Pages
- 285-300
- ISSN
- 1043-0342 (ISSN-L)
- 1557-7422
- PMC
- PMC3997092
- OpenAlex
- W1654741967
- Cited by
- 65
- References
- 226
- Citations by year
- 2026: 1 · 2025: 4 · 2024: 4 · 2023: 6 · 2022: 6 · 2021: 8 · 2020: 3 · 2019: 5 · 2018: 4 · 2017: 8 · 2016: 9 · 2015: 6 · 2014: 1
- FWCI
- 1.06
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Human Gene Therapy (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- RECERCAT (Consorci de Serveis Universitaris de Catalunya) (publishedVersion)
- ENLIGHTEN (Jurnal Bimbingan dan Konseling Islam) (acceptedVersion)
- Dipòsit Digital de la Universitat de Barcelona (Universitat de Barcelona) (submittedVersion, public-domain)
- Institutional Repository of the Ruđer Bošković Institute (Ruđer Bošković Institute) (submittedVersion, other-oa)
- Funders
- European Commission (290002)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Virus-based gene therapy research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Keywords
- neutralizing antibodies, gene therapy vectors, immunogenicity, viral tropism, gene delivery, transgene expression
- MeSH terms
- Adenoviridae, Adenoviridae Infections, Animals, Genetic Vectors, Humans, Immunity, Immunity, Innate, Genetic Therapy, Gene Transfer Techniques, Transgenes, Adaptive Immunity
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