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Epiretinal membrane in a subject after transvitreal delivery of palucorcel (CNTO 2476)

BACKGROUND: A 70-year-old woman with retinitis pigmentosa experienced an epiretinal membrane (ERM) formation and a tractional retinal detachment (RD) following subretinal administration of palucorcel (CNTO 2476), a novel human umbilical tissue-derived cell-based therapy, as part of a Phase I study....

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Autores principales: Spencer, Rand, Fisher, Steven, Lewis, Geoffrey P, Malone, Terri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5640410/
https://www.ncbi.nlm.nih.gov/pubmed/29070939
http://dx.doi.org/10.2147/OPTH.S140218
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author Spencer, Rand
Fisher, Steven
Lewis, Geoffrey P
Malone, Terri
author_facet Spencer, Rand
Fisher, Steven
Lewis, Geoffrey P
Malone, Terri
author_sort Spencer, Rand
collection PubMed
description BACKGROUND: A 70-year-old woman with retinitis pigmentosa experienced an epiretinal membrane (ERM) formation and a tractional retinal detachment (RD) following subretinal administration of palucorcel (CNTO 2476), a novel human umbilical tissue-derived cell-based therapy, as part of a Phase I study. The clinical course and results of a histologic examination of the ERM, which was peeled during surgery to repair the RD, are described here. METHODS: In this open-label, first-in-human, Phase I study (NCT00458575), two of seven subjects developed RD, with an ERM formation reported in a woman receiving a targeted dose of 3.0×10(5) palucorcel administered via a transvitreal route. A sample of the ERM was retained for analysis following the ERM peeling procedure. Clinical outcomes and ERM histology, based on immunocytochemistry analyses and fluorescence in situ hybridization (FISH) staining, were evaluated. RESULTS: We first noted the RD and formation of the ERM at 26 days after palucorcel administration. The ERM was cellular and contained multiple cell types, including Müller glial cells, immune cells, neurites, retinal pigment epithelial cells, and palucorcel. The majority of cells were not actively dividing. FISH staining showed a subset of Y chromosome-positive cells in the ERM from this woman, supporting the presence of palucorcel (derived from umbilical cord tissue of male neonate). Palucorcel did not differentiate into Müller glia, immune cells, neurites, or retinal pigment epithelial cells. DISCUSSION: The development of an ERM containing both subject (self) cells and palucorcel suggests that palucorcel egress in the vitreal cavity after retinotomy may contribute to ERM formation and RD and that an alternative delivery method will be required before further studies are conducted. Subsequent clinical research using alternative subretinal delivery methods for palucorcel in other indications suggests that membrane development does not occur when palucorcel is delivered without retinal perforation.
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spelling pubmed-56404102017-10-25 Epiretinal membrane in a subject after transvitreal delivery of palucorcel (CNTO 2476) Spencer, Rand Fisher, Steven Lewis, Geoffrey P Malone, Terri Clin Ophthalmol Original Research BACKGROUND: A 70-year-old woman with retinitis pigmentosa experienced an epiretinal membrane (ERM) formation and a tractional retinal detachment (RD) following subretinal administration of palucorcel (CNTO 2476), a novel human umbilical tissue-derived cell-based therapy, as part of a Phase I study. The clinical course and results of a histologic examination of the ERM, which was peeled during surgery to repair the RD, are described here. METHODS: In this open-label, first-in-human, Phase I study (NCT00458575), two of seven subjects developed RD, with an ERM formation reported in a woman receiving a targeted dose of 3.0×10(5) palucorcel administered via a transvitreal route. A sample of the ERM was retained for analysis following the ERM peeling procedure. Clinical outcomes and ERM histology, based on immunocytochemistry analyses and fluorescence in situ hybridization (FISH) staining, were evaluated. RESULTS: We first noted the RD and formation of the ERM at 26 days after palucorcel administration. The ERM was cellular and contained multiple cell types, including Müller glial cells, immune cells, neurites, retinal pigment epithelial cells, and palucorcel. The majority of cells were not actively dividing. FISH staining showed a subset of Y chromosome-positive cells in the ERM from this woman, supporting the presence of palucorcel (derived from umbilical cord tissue of male neonate). Palucorcel did not differentiate into Müller glia, immune cells, neurites, or retinal pigment epithelial cells. DISCUSSION: The development of an ERM containing both subject (self) cells and palucorcel suggests that palucorcel egress in the vitreal cavity after retinotomy may contribute to ERM formation and RD and that an alternative delivery method will be required before further studies are conducted. Subsequent clinical research using alternative subretinal delivery methods for palucorcel in other indications suggests that membrane development does not occur when palucorcel is delivered without retinal perforation. Dove Medical Press 2017-10-06 /pmc/articles/PMC5640410/ /pubmed/29070939 http://dx.doi.org/10.2147/OPTH.S140218 Text en © 2017 Spencer et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Spencer, Rand
Fisher, Steven
Lewis, Geoffrey P
Malone, Terri
Epiretinal membrane in a subject after transvitreal delivery of palucorcel (CNTO 2476)
title Epiretinal membrane in a subject after transvitreal delivery of palucorcel (CNTO 2476)
title_full Epiretinal membrane in a subject after transvitreal delivery of palucorcel (CNTO 2476)
title_fullStr Epiretinal membrane in a subject after transvitreal delivery of palucorcel (CNTO 2476)
title_full_unstemmed Epiretinal membrane in a subject after transvitreal delivery of palucorcel (CNTO 2476)
title_short Epiretinal membrane in a subject after transvitreal delivery of palucorcel (CNTO 2476)
title_sort epiretinal membrane in a subject after transvitreal delivery of palucorcel (cnto 2476)
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5640410/
https://www.ncbi.nlm.nih.gov/pubmed/29070939
http://dx.doi.org/10.2147/OPTH.S140218
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