GMP-Compliant Human Fetal Skin Fibroblasts for Wound Healing
Authors:
- Parisa GoodarziPGParisa Goodarzi
- Khadijeh FalahzadehKFKhadijeh Falahzadeh
- Hamidreza AghayanHAHamidreza Aghayan
- Fereshteh Mohamadi JahaniFJFereshteh Mohamadi Jahani
- Moloud PayabMPMoloud Payab
- Kambiz GilanyKGKambiz Gilany
- Fakher RahimFRFakher Rahim
- Bagher LarijaniBLBagher Larijani
- Akram Tayanloo BeikABAkram Tayanloo Beik
- Hossein AdibiHAHossein Adibi
- Babak ArjmandBABabak Arjmand
Open Access
- 14 July 2018
- journal article
- research article
- Published by Brieflands in Archives of Neuroscience
- Vol. 5 (3)
Abstract
Background: Among different kinds of cells involved in the wound healing process, fibroblasts play a pivotal role in the proliferation phase of this procedure wherein they induce the production of local growth factors and cytokines. Fetal fibroblasts with low immunogenic property and different wound healing process could be considered as a suitable alternative to neonatal foreskin cell based products in regenerative medicine and cell therapy. Cell therapy is an almost newly introduced method in the medical field and is also a challenging issue, which should assure the safety of the final product and the absence of viral or bacterial contamination with minimal immunogenic response. Therefore, based on current GMP (cGMP) principles, it is a matter of great importance to monitor raw materials’ quality and the conformity of all production procedures including cell culture, collection, and cryopreservation with validated standard operating procedures (SOPs). In the current study, we demonstrated the GMP-compatible and clinical-grade fetal fibroblast cells banking to be used for clinical applications. Methods: All steps of isolation and culturing and cryopreservation of fetal fibroblast cells were performed under the sterile condition according to cGMP guidelines in the clean room. During the cell culture procedures, bacteriological investigation was performed in order to identify the probable contamination of the samples. Results: Isolated fetal dermal fibroblasts were harvested and stored at early passages. The viability of fibroblasts was ≥ 98%, indicating successful establishment of fibroblast banking. Flow cytometry analysis has revealed the high purity of isolated and cultured fibroblastic population Karyotyping of fibroblasts at the 10th subculture shows a normal diploid male pattern. Conclusions: The manufactured cells, according to the highest level of safety are considered as the most appropriate treatment option for cellular therapy. Based-on the current evidence, clinical-grade fetal fibroblasts throw new light on efficient and prompt healing of acute and chronic wounds of any etiology. Keywords: Fibroblasts; GMP; Wound healingKeywords
This publication has 38 references indexed in Scilit:
- Fetal Fibroblasts and Keratinocytes with Immunosuppressive Properties for Allogeneic Cell-Based Wound TherapyPLOS ONE, 2013
- Comparison of Explant-Derived and Enzymatic Digestion-Derived MSCs and the Growth Factors from Wharton’s JellyBioMed Research International, 2013
- Derivation of Xeno-Free and GMP-Grade Human Embryonic Stem Cells – Platforms for Future Clinical ApplicationsPLOS ONE, 2012
- Production and validation of a good manufacturing practice grade human fibroblast line for supporting human embryonic stem cell derivation and cultureStem Cell Research & Therapy, 2012
- Biologicals and Fetal Cell Therapy for Wound and Scar ManagementISRN Dermatology, 2011
- Clinical grade cultivation of human Schwann cell, by the using of human autologous serum instead of fetal bovine serum and without growth factorsCell and Tissue Banking, 2011
- Clinical Protocols for the Isolation and Expansion of Mesenchymal Stromal CellsTransfusion Medicine and Hemotherapy, 2008
- Dermal fibroblasts derived from fetal and postnatal humans exhibit distinct responses to insulin like growth factorsBMC Developmental Biology, 2007
- Tissue engineered fetal skin constructs for paediatric burnsThe Lancet, 2005
- Establishment of Fibroblast CulturesCurrent Protocols in Cell Biology, 1998