Epiretinal membrane in a subject after transvitreal delivery of palucorcel (CNTO 2476)
Open accessAbstract
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: 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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Any reflux should be avoided because release of cells to the vitreous cavity can induce an immune response or lead to formation of epiretinal membranes.
“Ideally, any reflux should be avoided as release of cells to the vitreous cavity can induce an immune response or lead to the formation of epiretinal membranes (20, 26–29).”
From Subretinal therapy: technological solutions to surgical and immunological challenges (2022) · cites this paper as [26]
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References 15 · Cited by 16
- Authors
- Spencer, R., Fisher, S., Lewis, G. P., & Malone, T.
- Affiliations
- Texas Retina Associates (United States) (US)
- University of California, Santa Barbara (US)
- Janssen Research & Development (United States) (US)
- Corresponding author
- Malone, Terri
- ORCID
- Spencer, Rand
- Venue
- Clinical Ophthalmology
- Publisher
- Informa UK Limited
- Published
- 2017-10
- Volume
- Volume 11
- Pages
- 1797-1803
- ISSN
- 1177-5467 (ISSN-L)
- 1177-5483
- PMC
- PMC5640410
- OpenAlex
- W2762779723
- Cited by
- 16
- References
- 15
- Citations by year
- 2026: 2 · 2024: 2 · 2022: 3 · 2021: 5 · 2019: 2 · 2017: 2
- FWCI
- 0.84
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Clinical ophthalmology (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Dove Medical Press (Taylor and Francis Group) (submittedVersion, cc-by-nc)
- Topics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Retinal and Macular Surgery
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Retinal Development and Disorders
- Health Sciences › Medicine › Ophthalmology › Retinal Diseases and Treatments
- Keywords
- epiretinal membrane, cell therapy, retinal cell transplantation, subretinal injection, tractional retinal detachment, retinitis pigmentosa, umbilical cord tissue, Müller cells, retinal pigment epithelium, immunocytochemistry, fluorescence in situ hybridization, retinal perforation
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