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AAV-mediated FGF21 gene therapy extends health span and lifespan in aged mice through multi-tissue adaptations

By

Fatima Bosch1,2,3 Send email to [email protected]

1d ago· 56 min readenNews

Summary

This study demonstrates that a one-time muscle-directed AAV-mediated FGF21 gene therapy in aged and geriatric mice extends health span and lifespan. The treatment normalized body weight and adiposity, improved insulin sensitivity and glucose homeostasis, and induced whole-body tissue-specific adaptations including enhanced metabolic and mitochondrial function, restored proteostasis, and reduced inflammation, fibrosis, and amyloidosis. The therapy prevented multi-organ age-related pathology and maintained systemic cell fitness, offering a potential gerotherapeutic approach for extending health span.

Source

Twitter / XAAV-mediated FGF21 gene therapy extends health span and lifespan in aged mice through multi-tissue adaptationscell.com

Key quotes

· 3 pulled
Here, we demonstrated that aged and geriatric male and female mice treated with muscle-directed adeno-associated viral (AAV) vector-mediated fibroblast growth factor 21 (FGF21) gene therapy extended health span and lifespan with sustained organ benefits.
This treatment normalized body weight and adiposity, improved insulin sensitivity and glucose homeostasis.
Bosch and colleagues described that one-time AAV-FGF21 gene therapy in aged mice induced whole-body tissue-specific adaptations, including improved metabolic and mitochondrial function, restored proteostasis, and reduced adiposity, inflammation, fibrosis, and amyloidosis.
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Bosch and colleagues described that one-time AAV-FGF21 gene therapy in aged mice induced whole-body tissue-specific adaptations, including improved metabolic and mitochondrial function, restored proteostasis, and reduced adiposity, inflammation, fibrosis,

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