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Large gene delivery to the retina with AAV vectors: are we there yet?

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Fig. 1: Split AAV-based strategies to restore large gene expression.

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Acknowledgements

The authors are grateful to Graciana Diez-Roux (TIGEM Scientific Office) for the critical reading of the manuscript.

Funding

AA is funded by Fondazione Telethon, the European Research Council (ERC) (grant number 694323 “EYEGET”) and by the European Union Horizon 2020 and Marie Curie programs (grants number: 825825 “Upgrade” and 813490 “StarT”, respectively). IT receives funding from University of Naples Federico II, STAR Program.

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Correspondence to Alberto Auricchio.

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IT, PT and AA are co-inventors on patents related to both dual AAV and AAV intein vectors.

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Trapani, I., Tornabene, P. & Auricchio, A. Large gene delivery to the retina with AAV vectors: are we there yet?. Gene Ther 28, 220–222 (2021). https://doi.org/10.1038/s41434-020-0174-4

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