Cargando…
Posttransplant VEGFR1R2 Trap Eye Drops Inhibit Corneal (Lymph)angiogenesis and Improve Corneal Allograft Survival in Eyes at High Risk of Rejection
PURPOSE: To assess whether topical application of VEGFR1R2 Trap after corneal transplantation can impair corneal (lymph)angiogenesis and promote murine corneal allograft survival in eyes at high risk of rejection. METHODS: We used the murine model of suture-induced neovascularization and subsequent...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Association for Research in Vision and Ophthalmology
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9100603/ https://www.ncbi.nlm.nih.gov/pubmed/35533080 http://dx.doi.org/10.1167/tvst.11.5.6 |
_version_ | 1784706885978423296 |
---|---|
author | Zhang, Wei Schönberg, Alfrun Bock, Felix Cursiefen, Claus |
author_facet | Zhang, Wei Schönberg, Alfrun Bock, Felix Cursiefen, Claus |
author_sort | Zhang, Wei |
collection | PubMed |
description | PURPOSE: To assess whether topical application of VEGFR1R2 Trap after corneal transplantation can impair corneal (lymph)angiogenesis and promote murine corneal allograft survival in eyes at high risk of rejection. METHODS: We used the murine model of suture-induced neovascularization and subsequent keratoplasty in eyes at high risk of rejection, which is an established model for local drug application. After transplantation, the mice were treated with either VEGFR1R2 Trap (aflibercept) or human IgG Fc as eye drops for 2 weeks (three times/d). Deposition of VEGFR1R2 Trap in corneal tissue was detected by immunohistochemistry. Two and 8 weeks after transplantation, corneal (lymph)angiogenesis was assessed morphometrically. Dendritic cells (DCs) and regulatory T cells (Tregs) in the draining lymph nodes (dLNs) were examined by flow cytometry. Allograft survival was determined by corneal graft opacity scores. RESULTS: Topically applied VEGFR1R2 Trap penetrated into corneal host and graft stroma after keratoplasty in eyes at high risk of rejection. Additional postsurgical corneal hemangiogenesis (P < 0.0001) and lymphangiogenesis (P < 0.01) as well as infiltrating CD45(+) leukocytes (P < 0.001) and macrophages (P < 0.01) were significantly reduced in the VEGFR1R2 Trap group compared to controls. VEGFR1R2 Trap eye drops significantly decreased the frequency of total CD11c(+) DCs (P < 0.01), as well as activated CD11c(+)MHC II(+) DCs (P < 0.01) and CD11c(+)CD40(+) DCs (P < 0.05). In contrast, the frequency of CD200R(+) regulatory DCs (P < 0.05) and Tregs in dLNs (P < 0.01) was enhanced. Moreover, long-term allograft survival was also improved (P < 0.05). CONCLUSIONS: Temporary, topical application of VEGFR1R2 Trap after corneal transplantation can achieve sufficient anti-VEGF activity, inhibit additional (lymph)angiogenesis, and significantly improve corneal allograft survival in eyes at high risk of rejection. TRANSLATIONAL RELEVANCE: VEGFR1R2 Trap eye drops after transplantation present a new therapeutic option for patients undergoing corneal transplantation and are at high risk of graft rejection. |
format | Online Article Text |
id | pubmed-9100603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Association for Research in Vision and Ophthalmology |
record_format | MEDLINE/PubMed |
spelling | pubmed-91006032022-05-14 Posttransplant VEGFR1R2 Trap Eye Drops Inhibit Corneal (Lymph)angiogenesis and Improve Corneal Allograft Survival in Eyes at High Risk of Rejection Zhang, Wei Schönberg, Alfrun Bock, Felix Cursiefen, Claus Transl Vis Sci Technol Article PURPOSE: To assess whether topical application of VEGFR1R2 Trap after corneal transplantation can impair corneal (lymph)angiogenesis and promote murine corneal allograft survival in eyes at high risk of rejection. METHODS: We used the murine model of suture-induced neovascularization and subsequent keratoplasty in eyes at high risk of rejection, which is an established model for local drug application. After transplantation, the mice were treated with either VEGFR1R2 Trap (aflibercept) or human IgG Fc as eye drops for 2 weeks (three times/d). Deposition of VEGFR1R2 Trap in corneal tissue was detected by immunohistochemistry. Two and 8 weeks after transplantation, corneal (lymph)angiogenesis was assessed morphometrically. Dendritic cells (DCs) and regulatory T cells (Tregs) in the draining lymph nodes (dLNs) were examined by flow cytometry. Allograft survival was determined by corneal graft opacity scores. RESULTS: Topically applied VEGFR1R2 Trap penetrated into corneal host and graft stroma after keratoplasty in eyes at high risk of rejection. Additional postsurgical corneal hemangiogenesis (P < 0.0001) and lymphangiogenesis (P < 0.01) as well as infiltrating CD45(+) leukocytes (P < 0.001) and macrophages (P < 0.01) were significantly reduced in the VEGFR1R2 Trap group compared to controls. VEGFR1R2 Trap eye drops significantly decreased the frequency of total CD11c(+) DCs (P < 0.01), as well as activated CD11c(+)MHC II(+) DCs (P < 0.01) and CD11c(+)CD40(+) DCs (P < 0.05). In contrast, the frequency of CD200R(+) regulatory DCs (P < 0.05) and Tregs in dLNs (P < 0.01) was enhanced. Moreover, long-term allograft survival was also improved (P < 0.05). CONCLUSIONS: Temporary, topical application of VEGFR1R2 Trap after corneal transplantation can achieve sufficient anti-VEGF activity, inhibit additional (lymph)angiogenesis, and significantly improve corneal allograft survival in eyes at high risk of rejection. TRANSLATIONAL RELEVANCE: VEGFR1R2 Trap eye drops after transplantation present a new therapeutic option for patients undergoing corneal transplantation and are at high risk of graft rejection. The Association for Research in Vision and Ophthalmology 2022-05-09 /pmc/articles/PMC9100603/ /pubmed/35533080 http://dx.doi.org/10.1167/tvst.11.5.6 Text en Copyright 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. |
spellingShingle | Article Zhang, Wei Schönberg, Alfrun Bock, Felix Cursiefen, Claus Posttransplant VEGFR1R2 Trap Eye Drops Inhibit Corneal (Lymph)angiogenesis and Improve Corneal Allograft Survival in Eyes at High Risk of Rejection |
title | Posttransplant VEGFR1R2 Trap Eye Drops Inhibit Corneal (Lymph)angiogenesis and Improve Corneal Allograft Survival in Eyes at High Risk of Rejection |
title_full | Posttransplant VEGFR1R2 Trap Eye Drops Inhibit Corneal (Lymph)angiogenesis and Improve Corneal Allograft Survival in Eyes at High Risk of Rejection |
title_fullStr | Posttransplant VEGFR1R2 Trap Eye Drops Inhibit Corneal (Lymph)angiogenesis and Improve Corneal Allograft Survival in Eyes at High Risk of Rejection |
title_full_unstemmed | Posttransplant VEGFR1R2 Trap Eye Drops Inhibit Corneal (Lymph)angiogenesis and Improve Corneal Allograft Survival in Eyes at High Risk of Rejection |
title_short | Posttransplant VEGFR1R2 Trap Eye Drops Inhibit Corneal (Lymph)angiogenesis and Improve Corneal Allograft Survival in Eyes at High Risk of Rejection |
title_sort | posttransplant vegfr1r2 trap eye drops inhibit corneal (lymph)angiogenesis and improve corneal allograft survival in eyes at high risk of rejection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9100603/ https://www.ncbi.nlm.nih.gov/pubmed/35533080 http://dx.doi.org/10.1167/tvst.11.5.6 |
work_keys_str_mv | AT zhangwei posttransplantvegfr1r2trapeyedropsinhibitcorneallymphangiogenesisandimprovecornealallograftsurvivalineyesathighriskofrejection AT schonbergalfrun posttransplantvegfr1r2trapeyedropsinhibitcorneallymphangiogenesisandimprovecornealallograftsurvivalineyesathighriskofrejection AT bockfelix posttransplantvegfr1r2trapeyedropsinhibitcorneallymphangiogenesisandimprovecornealallograftsurvivalineyesathighriskofrejection AT cursiefenclaus posttransplantvegfr1r2trapeyedropsinhibitcorneallymphangiogenesisandimprovecornealallograftsurvivalineyesathighriskofrejection |