Optimized AAV capsids for diseases of the basal ganglia show robust potency and distribution in adult nonhuman primates

Leib, D. E.; Chen, Y. H.; Tecedor, L.; Ranum, P. T.; Keiser, M. S.; Lewandowshi, B. C.; Carrell, E. M.; Arora, S.; Huerta-Ocampo, I.; Liu, X.; Davidson, B. L.

doi:10.1101/2024.05.02.592211

bioRxiv · 10.1101/2024.05.02.592211

Optimized AAV capsids for diseases of the basal ganglia show robust potency and distribution in adult nonhuman primates

Leib, D. E.·Chen, Y. H.·Tecedor, L.·Ranum, P. T.·Keiser, M. S.·Lewandowshi, B. C.·Carrell, E. M.·Arora, S.·Huerta-Ocampo, I.·Liu, X.·Davidson, B. L.

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Abstract

Huntingtons disease and other disorders of the basal ganglia create challenges for biomolecule-based medicines given the poor accessibility of these deep brain structures following intracerebral or intravascular delivery. Additionally, for adeno-associated viruses (AAVs) intravascular delivery exposes peripheral tissues to the vast majority of the therapy, increasing the risk of immune responses and the quantity and associated cost of goods required for therapeutically relevant brain penetration levels. Here, we found that low dose, low volume delivery of unbiased AAV libraries into a focused brain region allowed recovery of novel capsids capable of broad access to key deep brain and cortical structures relevant for human therapies at doses orders of magnitude lower than used in current clinical trials. One such capsid, AAV-DB-3, provided transduction of up to 45% of medium spiny neurons in the adult NHP striatum, along with substantial transduction of relevant deep layer neurons in the cortex. Notably, AAV-DB-3 behaved similarly in mice as in NHPs and also potently transduced human neurons derived from induced pluripotent stem cells. Thus, AAV-DB-3 provides a unique AAV for network level brain gene therapies that translates up and down the evolutionary scale for preclinical studies and eventual clinical use.

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Leib, D. E., Chen, Y. H., Tecedor, L., Ranum, P. T., Keiser, M. S., Lewandowshi, B. C., Carrell, E. M., Arora, S., Huerta-Ocampo, I., Liu, X., Davidson, B. L.. 2024-05-05. Optimized AAV capsids for diseases of the basal ganglia show robust potency and distribution in adult nonhuman primates. https://doi.org/10.1101/2024.05.02.592211

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