Polarized RPE Secretome Preserves Photoreceptors in Retinal Dystrophic RCS Rats

Author:

Ahluwalia Kabir1ORCID,Martinez-Camarillo Juan-Carlos23,Thomas Biju B.23ORCID,Naik Aditya1,Gonzalez-Calle Alejandra23,Pollalis Dimitrios23ORCID,Lebkowski Jane4,Lee Sun Young235ORCID,Mitra Debbie2,Louie Stan G.12ORCID,Humayun Mark S.23

Affiliation:

1. Mann School of Pharmacy and Pharmaceutical Sciences, University of Southern California, Los Angeles, CA 90089, USA

2. USC Ginsburg Institute of for Biomedical Therapeutics, University of Southern California, Los Angeles, CA 90033, USA

3. USC Roski Eye Institute, Department of Ophthalmology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA

4. Regenerative Patch Technologies LLC, Menlo Park, CA 94028, USA

5. Department of Physiology & Neuroscience, Keck School of Medicine, University of Southern California, Los Angeles, CA 90089, USA

Abstract

Retinal degenerative diseases, including age-related macular degeneration (AMD) and retinitis pigmentosa, lack effective therapies. Conventional monotherapeutic approaches fail to target the multiple affected pathways in retinal degeneration. However, the retinal pigment epithelium (RPE) secretes several neurotrophic factors addressing diverse cellular pathways, potentially preserving photoreceptors. This study explored human embryonic stem cell-derived, polarized RPE soluble factors (PRPE-SF) as a combination treatment for retinal degeneration. PRPE-SF promoted retinal progenitor cell survival, reduced oxidative stress in ARPE-19 cells, and demonstrated critical antioxidant and anti-inflammatory effects for preventing retinal degeneration in the Royal College of Surgeons (RCS) rat model. Importantly, PRPE-SF treatment preserved retinal structure and scotopic b-wave amplitudes, suggesting therapeutic potential for delaying retinal degeneration. PRPE-SF is uniquely produced using biomimetic membranes for RPE polarization and maturation, promoting a protective RPE secretome phenotype. Additionally, PRPE-SF is produced without animal serum to avoid immunogenicity in future clinical development. Lastly, PRPE-SF is a combination of neurotrophic factors, potentially ameliorating multiple dysfunctions in retinal degenerations. In conclusion, PRPE-SF offers a promising therapeutic candidate for retinal degenerative diseases, advancing the development of effective therapeutic strategies for these debilitating conditions.

Funder

California Institute for Regenerative Medicine

Unrestricted Grant to the Department of Ophthalmology from Research to Prevent Blindness, New York, NY

National Eye Institute of the National Institutes of Health

Dr. Allen and Charlotte Ginsburg Institute for Biomedical Therapeutics

Dennis and Michele Slivinski

The USC Roski Eye Institute

The Marcus Foundation, Inc.

Dr. Ramani Nathan

The Retina Research Foundation’s Gertrude D. Pyron Award

Publisher

MDPI AG

Subject

General Medicine

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