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Pigment Epithelium-Derived Factor as a possible predictor of corneal transplant rejection reaction

https://doi.org/10.21516/2072-0076-2026-19-2-164-169

Abstract

Keratoplasty remains one of the most effective methods of restoring vision in diseases and injuries of the eye that lead to the cornea opacity. Despite the success of modern surgery, corneal transplant rejection is the most common cause of unsuccessful operations. Pigmented epithelial derivative factor (PEDF) is known for its antiangiogenic and anti-inflammatory properties, which play an important role in maintaining the immune privilege of the eye and make it one of the important regulators of the intraocular environment. Purpose of the work was to study the concentration of PEDF in the tear fluid (TF) after penetrating keratoplasty and to evaluate its role in the development of the corneal transplant rejection reaction. Material and methods. 48 patients aged 35 to 60 years (average age of 48.1 ± 5.4) including 30 men and 18 women participated in the study. Subgroup 1 (n = 35) consisted of patients who had no episodes of corneal transplant rejection during the observed period, subgroup 2 (n = 13) consisted of patients who demonstrated an episode of rejection reaction during one year after surgery. The control group included 15 healthy individuals without ophthalmological pathology. The level of PEDF (ng/ml) in the TF was determined during postoperative period using multiplex analysis on a Luminex Magpix 100 immunoanalyzer (USA) by the Bio-Rad multiplex analysis test system (USA). The graft condition was assessed using biomicroscopy and optical coherence tomography with angiography of the anterior segment. Results. In postoperative period a significant increase in the volume of vascularization with a maximum increase on day 360 in subgroup 2 was revealed. The concentration of PEDF in subgroup 1 increased to reference values on day 120, while maintaining this level at the end of the study. On the contrary, in subgroup 2, the PEDF level remained reduced until the end of the follow-up period and significantly differed from the indicator of the control group, which, along with an increase in the volume of vascularization and a progressive decrease in maximally corrected visual acuity, may indicate a violation of control over the processes of neovascularization and contribute to graft rejection. Conclusion. Given the crucial role of PEDF in curbing corneal neoangiogenesis, its decrease can be considered as a predictor of the development of a graft rejection reaction, as evidenced by the data we have obtained.

About the Authors

A. M. Bystrov
The Chelyabinsk Regional Clinical Hospital; South-Ural State Medical University
Russian Federation

Aleksey M. Bystrov — researcher of the ophthalmology department, The Chelyabinsk Regional Clinical Hospital; laboratory assistant at the department of medical rehabilitation and sports medicine, South-Ural State Medical University.

70, Vorovskogo St., Chelyabinsk, 454048; 64, Vorovskogo St., Chelyabinsk, 454141



A. A. Kuznetzov
The Chelyabinsk Regional Clinical Hospital
Russian Federation

Andrey A. Kuznetzov — Cand. of Med. Sci., head of the ophthalmology center.

70, Vorovskogo St., Chelyabinsk, 454048



E. V. Davydova
The Chelyabinsk Regional Clinical Hospital; South-Ural State Medical University
Russian Federation

Evgeniya V. Davydova — Dr. of Med. Sci., associate professor, head of the department of early medical rehabilitation, The Chelyabinsk Regional Clinical Hospital; professor of the department of medical rehabilitation and sports medicine, South-Ural State Medical University.

70, Vorovskogo St., Chelyabinsk, 454048; 64, Vorovskogo St., Chelyabinsk, 454141



T. V. Gavrilova
Perm State Medical University named after Academician E.A. Wagner
Russian Federation

Tatyana V. Gavrilova — Dr. of Med. Sci., professor, corresponding member of the Russian Academy of Sciences, head of the department of ophthalmology.

26, Petropavlovskaya St., Perm, 614990



References

1. Bystrov A.M., Kuznetsov A.A. Dynamics of VEGF and TGF-β indices in tear fluid as a predictor of corneal transplant rejection. Russian journal of immunology. 2025; 28 (1): 103–8 (In Russ.). doi: 10.46235/1028-7221-16977-DOV

2. Patnam M, Dommaraju SR, Masood F, et al. Lymphangiogenesis guidance mechanisms and therapeutic implications in pathological states of the cornea. Cells. 2023; 12 (2): 319. doi: 10.3390/cells12020319

3. Hori J, Yamaguchi T, Keino H, Hamrah P, Maruyama K. Immune privilege in corneal transplantation. Prog Retin Eye Res. 2019; 9 (72): 55–61. doi: 10.1016/j.preteyeres.2019.04.002

4. Schönberg A, Hamdorf M, Bock F. Immunomodulatory strategies targeting dendritic cells to improve corneal graft survival. J Clin Med. 2020; 5 (283): 1280. doi: 10.3390/jcm9051280

5. Major J, Foroncewicz B, Szaflik JP, Mucha K. Immunology and donor-specific antibodies in corneal transplantation. Archivum Immunologiae et Therapiae Experimentalis. 2021; 11 (69): 32. doi: 10.1007/s00005-021-00636-3

6. Ma B, Zhou Y, Liu R, et al. Pigment epithelium-derived factor (PEDF) plays anti-inflammatory roles in the pathogenesis of dry eye disease. The ocular surface. 2021; 20: 70–85. doi: 10.1016/j.jtos.2020.12.007

7. Mohan RR, Gupta S, Kumar R, et al. Tissue-targeted and localized AAV5-DCN and AAV5-PEDF combination gene therapy abrogates corneal fibrosis and concurrent neovascularization in rabbit eyes in vivo. The Ocular Surface. 2024; 32: 13–25. doi: 10.1016/j.jtos.2024.01.001

8. Moroz Z.I. Keratoplasty and keratoprosthetics. In: Avetisov S.E., Egorov E.A., Moshetova L.K., eds. National Guidelines for Ophthalmology. Moscow: GEOTAR-Media; 2008: 472–4 (In Russ.).

9. Chu X, Yin Y, Chen S, et al. Suppressive role of Pigment Epithelium-derived Factor in a rat model of corneal allograft rejection. Transplantation. 2024; 108 (10): 2072–83. doi: 10.1097/TP.0000000000005032

10. Drzyzga Ł, Śpiewak D, Dorecka M, Wyględowska-Promieńska D. Available therapeutic options for corneal neovascularization: A review. International Journal of Molecular Science. 2024; 25 (10): 5479. doi: 10.3390/ijms25105479

11. Yamagishi SI, Matsui T. Pigment epithelium-derived factor: a novel therapeutic target for cardiometabolic diseases and related complications. Current Medicinal Chemistry. 2018; 25 (13): 1480–500.

12. Yeh SI, Yu SH, Chu HS, et al. Pigment epithelium-derived factor peptide promotes corneal nerve regeneration: an in vivo and in vitro study. Invest Ophthalmol Vis Sci. 2021 Jan 4; 62 (1): 23. doi: 10.1167/iovs.62.1.23

13. Maharana PK, Mandal S, Kaweri L, et al. Immunopathogenesis of corneal graft rejection. Indian Journal of Ophthalmology. 2023; 71 (5): 1733–8. doi: 10.4103/IJO.IJO_2866_22

14. Mandal S, Maharana PK, Kaweri L, et al. Management and prevention of corneal graft rejection. Indian Journal of Ophthalmology. 2023; 71 (9): 3149–59. doi: 10.4103/IJO.IJO_228_23

15. Patnam M, Dommaraju SR, Masood F, et al. Lymphangiogenesis guidance mechanisms and therapeutic implications in pathological states of the cornea. Cells. 2023; 12 (2): 319. doi: 10.3390/cells12020319

16. Chen S, Barnstable CJ, Zhang X, et al. A PEDF peptide mimetic effectively relieves dry eye in a diabetic murine model by restoring corneal nerve, barrier, and lacrimal gland function. Ocul Surf. 2024; 32: 1–12. doi: 10.1016/j.jtos.2023.12.002

17. Di Zazzo A, Gaudenzi D, Yin J, et al. Corneal angiogenic privilege and its failure. Exp Eye Res. 2021; 204: 108457. doi: 10.1016/j.exer.2021.108457

18. Tartey, S., Takeuchi O. Pathogen recognition and Toll-like receptor targeted therapeutics in innate immune cells. Int Rev Immunol. 2017; 6: 1–17. doi: 10.1080/08830185.2016.1261318


Review

For citations:


Bystrov A.M., Kuznetzov A.A., Davydova E.V., Gavrilova T.V. Pigment Epithelium-Derived Factor as a possible predictor of corneal transplant rejection reaction. Russian Ophthalmological Journal. 2026;19(2):164-169. (In Russ.) https://doi.org/10.21516/2072-0076-2026-19-2-164-169

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ISSN 2072-0076 (Print)
ISSN 2587-5760 (Online)