Engineering humoral immunity as prophylaxis or therapy
Open accessAbstract
Purpose of the review In this review, we will discuss the field of engineered humoral immunity with an emphasis on recent work using viral vectors to produce antibodies in vivo. As an alternative to passive transfer of monoclonal antibody protein, a transgene encoding an antibody is delivered to cells via vector transduction, resulting in expression and secretion by the host cell. This review will summarize the evidence in support of this strategy as an alternative to traditional vaccines against infection and as novel therapeutics for a variety of diseases.Recent findings Historically, humoral immunity has been engineered through vaccination and passive transfer of monoclonal antibodies. However, recent work suggests that vectors can be used to deliver transgenes encoding broadly neutralizing antibodies to non-hematopoietic tissues and can mediate long-term expression that is capable of preventing or treating infectious diseases. The production of engineered monoclonal antibodies allows for precise targeting and elimination of aberrant self-proteins that are characteristic of certain neurodegenerative disease. This approach has also been successfully used to combat cancer and addiction in several animal models. Despite the wide array of expression platforms that have been described, adeno-associated virus vectors have emerged as the frontrunner for rapid clinical translation.Summary Recent advances in vector-mediated antibody expression have demonstrated the potential for such interventions to prevent infection and treat disease. As such, it offers an alternative to immunogen-based vaccine design and a novel therapeutic intervention by enabling precise manipulation of humoral immunity. Success translating these approaches to patients may enable the development of effective prevention against previously intractable pathogens that evade immunity such as HIV, influenza, malaria or HCV and may also enable new treatment options for neurodegenerative diseases such as Alzheimer's disease.
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For safety reasons, transient vectors or regulated expression would be preferred for clinical use.
“for safety reasons, transient vectors or regulated expression would be preferred for clinical use (Deal & Balazs, 2015).”
From mRNA mediates passive vaccination against infectious agents, toxins, and tumors (2017) · cites this paper as Deal & Balazs, 2015
The “Vectored Antibody Delivery for Cancer” section (page unavailable) says clinical translation of vectored antibody delivery for cancer will require transient vectors or regulated mAb delivery. The claim extends that recommendation to clinical use generally and gives safety as the reason, which the passage does not explicitly state. (LLM, conf=0.86)
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References 61 · Cited by 27
- Authors
- Deal, C. E., & Balazs, A. B.
- Affiliations
- Ragon Institute of MGH, MIT and Harvard (US)
- Corresponding author
- Balazs, Alejandro B
- ORCID
- Balazs, Alejandro B
- Venue
- Current Opinion in Immunology
- Publisher
- Elsevier BV
- Published
- 2015-08
- Volume
- 35
- Pages
- 113-122
- ISSN
- 0952-7915 (ISSN-L)
- PMC
- PMC4553141
- OpenAlex
- W910576623
- Cited by
- 27
- References
- 61
- Citations by year
- 2025: 2 · 2023: 1 · 2022: 2 · 2021: 2 · 2020: 2 · 2019: 6 · 2018: 4 · 2017: 6 · 2016: 1 · 2015: 1
- FWCI
- 0.51
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Current Opinion in Immunology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Allergy and Infectious Disease
- National Institutes for Drug Abuse
- William F. Milton Fund
- Charles H. Hood Foundation
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Virus-based gene therapy research
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Monoclonal and Polyclonal Antibodies Research
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Keywords
- viral vectors, adeno-associated virus vectors, broadly neutralizing antibodies, passive antibody transfer, vaccine alternatives, cancer immunotherapy, addiction treatment, neurodegenerative diseases, Alzheimer's disease, HIV, influenza, malaria, hepatitis C virus
- MeSH terms
- Animals, Genetic Vectors, Humans, Immunotherapy, Infections, Vaccines, Protein Engineering, Transgenes, Immunity, Humoral, Antibodies, Neutralizing
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