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Journal article

Inducible nonhuman primate models of retinal degeneration for testing end-stage therapies

Abstract:
The anatomical differences between the retinas of humans and most animal models pose a challenge for testing novel therapies. Nonhuman primate (NHP) retina is anatomically closest to the human retina. However, there is a lack of relevant NHP models of retinal degeneration (RD) suitable for preclinical studies. To address this unmet need, we generated three distinct inducible cynomolgus macaque models of RD. We developed two genetically targeted strategies using optogenetics and CRISPR-Cas9 to ablate rods and mimic rod-cone dystrophy. In addition, we created an acute model by physical separation of the photoreceptors and retinal pigment epithelium using a polymer patch. Among the three models, the CRISPR-Cas9–based approach was the most advantageous model in view of recapitulating disease-specific features and its ease of implementation. The acute model, however, resulted in the fastest degeneration, making it the most relevant model for testing end-stage vision restoration therapies such as stem cell transplantation.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1126/sciadv.adg8163

Authors

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Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Author
ORCID:
0000-0002-9122-5998
More by this author
Role:
Author
ORCID:
0009-0001-6889-1183
More by this author
Role:
Author
ORCID:
0009-0009-1703-9415


Publisher:
American Association for the Advancement of Science
Journal:
Science Advances More from this journal
Volume:
9
Issue:
31
Article number:
eadg8163
Publication date:
2023-08-04
Acceptance date:
2023-06-29
DOI:
EISSN:
2375-2548


Language:
English
Pubs id:
2430815
Local pid:
pubs:2430815
Source identifiers:
W4385481045
Deposit date:
2026-06-07
ARK identifier:

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