Details

Autor(en) / Beteiligte

• Cabanes-Creus, Marti
• Liao, Sophia H Y
• Gale Navarro, Renina
• Knight, Maddison
• Nazareth, Deborah
• Lau, Ngee-Soon
• Ly, Mark
• Zhu, Erhua
• Roca-Pinilla, Ramon
• Bugallo Delgado, Ricardo
• Vicente, Ana F
• Baltazar, Grober
• Westhaus, Adrian
• Merjane, Jessica
• Crawford, Michael
• McCaughan, Geoffrey W
• Unzu, Carmen
• González-Aseguinolaza, Gloria
• Alexander, Ian E
• Pulitano, Carlo
• Lisowski, Leszek

Titel

Harnessing whole human liver ex situ normothermic perfusion for preclinical AAV vector evaluation

Ist Teil von

• Nature communications, 2024-03, Vol.15 (1), p.1876-1876

Ort / Verlag

England: Nature Publishing Group

Erscheinungsjahr

2024

Link zum Volltext

Quelle

MEDLINE

Beschreibungen/Notizen

• Developing clinically predictive model systems for evaluating gene transfer and gene editing technologies has become increasingly important in the era of personalized medicine. Liver-directed gene therapies present a unique challenge due to the complexity of the human liver. In this work, we describe the application of whole human liver explants in an ex situ normothermic perfusion system to evaluate a set of fourteen natural and bioengineered adeno-associated viral (AAV) vectors directly in human liver, in the presence and absence of neutralizing human sera. Under non-neutralizing conditions, the recently developed AAV variants, AAV-SYD12 and AAV-LK03, emerged as the most functional variants in terms of cellular uptake and transgene expression. However, when assessed in the presence of human plasma containing anti-AAV neutralizing antibodies (NAbs), vectors of human origin, specifically those derived from AAV2/AAV3b, were extensively neutralized, whereas AAV8- derived variants performed efficiently. This study demonstrates the potential of using normothermic liver perfusion as a model for early-stage testing of liver-focused gene therapies. The results offer preliminary insights that could help inform the development of more effective translational strategies.