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bioRxiv · 10.1101/2021.09.27.461256

Quantitative single-cell transcriptome-based ranking of engineered AAVs in human retinal explants

Xi, Z.·Ozturk, B. E.·Johnson, M. E.·Byrne, L. C.
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Abstract

Gene therapy is a rapidly developing field, and adeno-associated virus (AAV) is a leading viral vector candidate for therapeutic gene delivery. Newly engineered AAVs with improved abilities are now entering the clinic. It has proven challenging, however, to predict the translational potential of gene therapies developed in animal models, due to cross-species differences. Human retinal explants are the only available model of fully developed human retinal tissue, and are thus important for the validation of candidate AAV vectors. In this study, we evaluated 18 wildtype and engineered AAV capsids in human retinal explants using a recently developed single-cell RNA-Seq AAV engineering pipeline (scAAVengr). Human retinal explants retained the same major cell types as fresh retina, with similar expression of cell-specific markers, except for a cone population with altered expression of cone-specific genes. The efficiency and tropism of AAVs in human explants were quantified, with single-cell resolution. The top performing serotypes, K91, K912, and 7m8, were further validated in non-human primate and human retinal explants. Together, this study provides detailed information about the transcriptome profiles of retinal explants, and quantifies the infectivity of leading AAV serotypes in human retina, accelerating the translation of retinal gene therapies to the clinic. Graphic abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=156 SRC="FIGDIR/small/461256v2_ufig1.gif" ALT="Figure 1"> View larger version (29K): org.highwire.dtl.DTLVardef@1e110ddorg.highwire.dtl.DTLVardef@11a2c7eorg.highwire.dtl.DTLVardef@15f1633org.highwire.dtl.DTLVardef@1aa741a_HPS_FORMAT_FIGEXP M_FIG C_FIG

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Xi, Z., Ozturk, B. E., Johnson, M. E., Byrne, L. C.. 2021-09-27. Quantitative single-cell transcriptome-based ranking of engineered AAVs in human retinal explants. https://doi.org/10.1101/2021.09.27.461256

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