Reduction of pathological retinal neovascularization, vessel obliteration, and artery tortuosity by PEDF protein in an oxygen-induced ischemic retinopathy rat model.

OIR rat model PEDF protein therapy ROP angiogenesis artery tortuosity vessel obliteration

Journal

FASEB bioAdvances
ISSN: 2573-9832
Titre abrégé: FASEB Bioadv
Pays: United States
ID NLM: 101733210

Informations de publication

Date de publication:
Sep 2024
Historique:
received: 10 04 2024
revised: 20 06 2024
accepted: 02 07 2024
medline: 14 10 2024
pubmed: 14 10 2024
entrez: 14 10 2024
Statut: epublish

Résumé

Retinopathy of prematurity (ROP) is a severe retinal disease in premature infants characterized by pathological neovascularization, obliteration of retinal vessels and increased vessel tortuosity. Currently, there are no completely satisfactory treatments for ROP. Pigment epithelium-derived factor (PEDF), a potent inhibitor of angiogenesis, appears late in gestation and its deficiency may be linked to development of ROP. This study investigates the preclinical efficacy of PEDF protein alone or in combination with VEGF antagonists for treating ROP. The safety of PEDF protein in the rat eye was assessed using functional in vivo measurements and histology. The efficacy of intravitreal injections (IVI) of various treatments was evaluated in a rat oxygen-induced retinopathy (OIR) model using in vivo imaging and flatmount analyses. No functional or histological side-effects were found in rat eyes after intravitreal PEDF protein injection. PEDF protein alone or combined with anti-VEGF drugs significantly reduced pathological neovascularization and vessel obliteration, comparable to the effects of anti-VEGF drugs alone. Regarding arterial tortuosity, treatment with a combination of PEDF, and VEGF antagonist was more effective than treatment with anti-VEGF alone. IVI of PEDF protein is safe. PEDF protein alone or combined with VEGF antagonists shows similar efficacy in reducing pathological neovascularization and vessel obliteration as anti-VEGF agents. Furthermore, only treatments involving PEDF protein, alone or with VEGF antagonists, significantly improved the quality of retinal vasculature. Thus, PEDF protein alone or combined with anti-VEGF agents presents a promising alternative to current anti-VEGF treatments for ROP.

Identifiants

pubmed: 39399476
doi: 10.1096/fba.2024-00059
pii: FBA21456
pmc: PMC11467744
doi:

Types de publication

Journal Article

Langues

eng

Pagination

311-326

Informations de copyright

©2024 The Authors FASEB BioAdvances published by The Federation of American Societies for Experimental Biology.

Déclaration de conflit d'intérêts

SZ, AT, SSK, KW, SK and SJS have no competing interests to declare that are relevant to the content of this article. US is holder of a patent.

Auteurs

Shiying Zhao (S)

Division of Experimental Vitreoretinal Surgery, Centre for Ophthalmology, Institute for Ophthalmic Research University Medical Center, Eberhard Karls University of Tuebingen Tuebingen Germany.
Present address: Molecular mechanisms driving age-related macular degeneration, Experimental Vitreoretinal Surgery Group Centre for Ophthalmology, Institute for Ophthalmic Research, University Medical Center, Eberhard Karls University of Tuebingen Tuebingen Germany.

Alexander V Tschulakow (AV)

Division of Experimental Vitreoretinal Surgery, Centre for Ophthalmology, Institute for Ophthalmic Research University Medical Center, Eberhard Karls University of Tuebingen Tuebingen Germany.
OcuTox GmbH Preclinical Drug Assessment Hechingen Germany.
Present address: Molecular mechanisms driving age-related macular degeneration, Experimental Vitreoretinal Surgery Group Centre for Ophthalmology, Institute for Ophthalmic Research, University Medical Center, Eberhard Karls University of Tuebingen Tuebingen Germany.

Subha S Karthikeyan (SS)

Department of Gene Therapy University Clinic Ulm Germany.

Kun Wang (K)

Division of Experimental Vitreoretinal Surgery, Centre for Ophthalmology, Institute for Ophthalmic Research University Medical Center, Eberhard Karls University of Tuebingen Tuebingen Germany.
Present address: Molecular mechanisms driving age-related macular degeneration, Experimental Vitreoretinal Surgery Group Centre for Ophthalmology, Institute for Ophthalmic Research, University Medical Center, Eberhard Karls University of Tuebingen Tuebingen Germany.

Stefan Kochanek (S)

Department of Gene Therapy University Clinic Ulm Germany.

Ulrich Schraermeyer (U)

Division of Experimental Vitreoretinal Surgery, Centre for Ophthalmology, Institute for Ophthalmic Research University Medical Center, Eberhard Karls University of Tuebingen Tuebingen Germany.
OcuTox GmbH Preclinical Drug Assessment Hechingen Germany.

Sylvie Julien-Schraermeyer (S)

Division of Experimental Vitreoretinal Surgery, Centre for Ophthalmology, Institute for Ophthalmic Research University Medical Center, Eberhard Karls University of Tuebingen Tuebingen Germany.
OcuTox GmbH Preclinical Drug Assessment Hechingen Germany.
Present address: Molecular mechanisms driving age-related macular degeneration, Experimental Vitreoretinal Surgery Group Centre for Ophthalmology, Institute for Ophthalmic Research, University Medical Center, Eberhard Karls University of Tuebingen Tuebingen Germany.

Classifications MeSH