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Engineering humoral immunity as prophylaxis or therapy.
Cailin E Deal1, Alejandro B Balazs1
1Ragon Institute of MGH, MIT & Harvard, 400 Technology Sq., Cambridge, MA 02139, United States.
Current Opinion in Immunology
|July 18, 2015
Summary
Engineered humoral immunity using viral vectors enables in vivo antibody production as an alternative to traditional vaccines and passive antibody therapies. This approach shows promise for preventing infections and treating diseases like cancer and neurodegeneration.
Area of Science:
- Immunology
- Gene Therapy
- Molecular Biology
Background:
- Humoral immunity is traditionally engineered via vaccination or monoclonal antibody (mAb) transfer.
- Engineered antibodies offer precise targeting for disease intervention.
Purpose of the Study:
- To review the field of engineered humoral immunity, focusing on viral vector-mediated in vivo antibody production.
- To explore this strategy as an alternative to traditional vaccines and as novel therapeutics.
Main Methods:
- Delivery of antibody-encoding transgenes via viral vectors for host cell expression and secretion.
- Utilizing adeno-associated virus (AAV) vectors for clinical translation.
Main Results:
- Viral vectors can mediate long-term expression of broadly neutralizing antibodies for disease prevention and treatment.
- Successful application in animal models for infectious diseases, neurodegenerative disorders, cancer, and addiction.
- Adeno-associated virus vectors are leading platforms for clinical translation.
Conclusions:
- Vector-mediated antibody expression presents a novel therapeutic strategy for precise manipulation of humoral immunity.
- Potential for preventing intractable infectious diseases (e.g., HIV, malaria, HCV) and treating neurodegenerative conditions (e.g., Alzheimer's disease).
- Offers an alternative to conventional immunogen-based vaccine design.
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