May 23, 2025 (press release) –
Key Highlights:
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* AAV.CPP.16 outperformed previous versions (AAV6 and AAV9) in cell culture, mouse models, and non-human primate models, showing promise for respiratory and lung gene therapy.
* The new tool was used to deliver scar-preventing gene therapy for pulmonary fibrosis and gene therapy for a viral infection, preventing the replication of the SARS-CoV-2 virus in a mouse model of COVID-19.
Original Press Release:
For gene therapy to work well, therapeutic molecules need to be efficiently delivered to the correct locations in the body—a job commonly given to adeno-associated viruses (AAV).
To improve the AAV’s ability to deliver therapeutics specifically to the lungs and airway,
“We noticed that AAV.CPP.16, which we initially engineered to enter the central nervous system, also efficiently targeted lung cells,” said senior author
The researchers found AAV.CPP.16 outperformed previous versions (AAV6 and AAV9) in cell culture, mouse models, and non-human primate models. They then used the more efficient tool to deliver scar-preventing gene therapy for pulmonary fibrosis, using a mouse model of the respiratory disease. They also used the tool to delivery gene therapy for a viral infection, where the therapy prevented the replication of the SARS-CoV-2 virus in a mouse model of COVID-19.
“Although further research is needed, our findings suggest that intranasal AAV.CPP.16 has strong translational potential as a promising delivery tool for targeting the airway and lung,” said
Authorship: In addition to Bei,
Disclosures: Bei is a co-founder of and scientific advisor to
Funding: This study was supported by Brigham and Women’s Hospital sundry fund, the
Paper cited: Yang Z, et al. “Cross-species tropism of AAV.CPP.16 in the respiratory tract and its gene therapies against pulmonary fibrosis and viral infection” Cell Reports Medicine DOI: 10.1016/j.xcrm.2025.102144
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