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A Full Good Manufacturing Practice-Compliant Protocol for Corneal Stromal Stem Cell Cultivation.
Santra, Mithun; Hsu, Yen-Michael S; Khadem, Shaheen; Radencic, Sydney; Funderburgh, Martha L; Sawant, Onkar B; Dhaliwal, Deepinder K; Jhanji, Vishal; Yam, Gary H F.
Affiliation
  • Santra M; Corneal Regeneration Laboratory, Department of Ophthalmology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Hsu YS; Immunologic Monitoring and Cellular Products Laboratory, Hillman Cancer Centre, University of Pittsburgh, Pittsburgh, PA, USA.
  • Khadem S; Center for Cell and Gene Therapy, Gift of Life Marrow Registry, Boca Raton, FL, USA.
  • Radencic S; Immunologic Monitoring and Cellular Products Laboratory, Hillman Cancer Centre, University of Pittsburgh, Pittsburgh, PA, USA.
  • Funderburgh ML; Immunologic Monitoring and Cellular Products Laboratory, Hillman Cancer Centre, University of Pittsburgh, Pittsburgh, PA, USA.
  • Sawant OB; Corneal Regeneration Laboratory, Department of Ophthalmology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Dhaliwal DK; Center for Vision and Eye Banking Research, Eversight, Cleveland, OH, USA.
  • Jhanji V; Corneal Regeneration Laboratory, Department of Ophthalmology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Yam GHF; Corneal Regeneration Laboratory, Department of Ophthalmology, University of Pittsburgh, Pittsburgh, PA, USA.
Bio Protoc ; 14(18): e5074, 2024 Sep 20.
Article in En | MEDLINE | ID: mdl-39346761
ABSTRACT
Corneal scarring, a significant cause of global blindness, results from various insults, including trauma, infections, and genetic disorders. The conventional treatment to replace scarred corneal tissues includes partial or full-thickness corneal transplantation using healthy donor corneas. However, only 1 in 70 individuals with treatable corneal scarring can undergo surgery, due to the limited supply of transplantable donor tissue. Our research focuses on cell-based strategies, specifically ex vivo-expanded corneal stromal stem cells (CSSCs), to address corneal scarring. Preclinical studies have demonstrated the efficacy of CSSC treatment in reducing corneal inflammation and fibrosis, inhibiting scar formation, and regenerating native stromal tissue. Mechanisms include CSSC differentiation into stromal keratocytes and the expression of regenerative cytokines. Here, we present a good manufacturing practice (GMP)-compliant protocol to isolate and expand human CSSCs. This method paves the way to produce clinical-grade CSSCs for transplantation and clinical trials. Key features • This protocol utilizes surgical skills to dissect human corneal tissues for CSSC isolation. • The yield and features of CSSCs rely on donor tissue quality (freshness) and have donor-to-donor variability. • Up to 0.5 billion CSSCs can be generated from a single cornea specimen, and cells at passage 3 are suitable for treatment uses.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Bio Protoc Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Bio Protoc Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States