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Exp Eye Res. 2014 Feb;119:27-34. doi: 10.1016/j.exer.2013.12.005. Epub 2013 Dec 15.

Effects of heat-treatment on plasma rich in growth factors-derived autologous eye drop.

Author information

1
Biotechnology Institute (BTI), Vitoria, Spain. Electronic address: eduardoanitua@eduardoanitua.com.
2
Biotechnology Institute (BTI), Vitoria, Spain.
3
Fundación de Investigación Oftalmológica, Instituto Oftalmológico Fernández-Vega, Oviedo, Spain.
4
Biotechnology Institute (BTI), Vitoria, Spain. Electronic address: gorka.orive@bti-implant.es.

Abstract

We have developed and characterized a new type of plasma rich in growth factors (PRGF) derived eye-drop therapy for patients suffering from autoimmune diseases. To determine the concentration of several growth factors, proteins, immunoglobulins and complement activity of the heat-inactivated eye-drop and to study its biological effects on cell proliferation and migration of different ocular surface cells, blood from healthy donors was collected, centrifuged and PRGF was prepared avoiding the buffy coat. The half volume of the obtained plasma supernatant from each donor was heat-inactivated at 56 °C for 1 h (heat-inactivated PRGF). The concentration of several proteins involved on corneal wound healing, immunoglubolins G, M and E and functional integrity of the complement system assayed by CH50 test were determined. The proliferative and migratory potential of inactivated and non-inactivated PRGF eye drops were assayed on corneal epithelial cells (HCE), keratocytes (HK) and conjunctival fibroblasts (HConF). Heat-inactivated PRGF preserves the content of most of the proteins and morphogens involved in its wound healing effects while reduces drastically the content of IgE and complement activity. Heat-inactivated PRGF eye drops increased proliferation and migration potential of ocular surface cells with regard to PRGF showing significant differences on proliferation and migration rate of HCE and HConF respectively. In summary, heat-inactivation of PRGF eye drops completely reduced complement activity and deceased significantly the presence of IgE, maintaining the biological activity of PRGF on ocular surface cells.

KEYWORDS:

EGF; ELISA; FBS; Fab fragment; Fc fragment; HCE; HConF; HK; IGF-I; IgE; IgG; IgM; Inact-PRGF; PBS; PDGF; PETIA; PRGF; PRP; TGF-β1; VEGF; autoimmune diseases; constant fragment of immunoglogulins; enzyme-linked immunosorbent assay; epithelial growth factor; fetal bovine serum; heat-inactivation; heat-treatment; human conjunctival fibroblasts; human corneal epithelial cells; human keratocytes; immunoglobulin E; immunoglobulin G; immunoglobulin M; inactivated PRGF; insulin-like growth factor I; ocular surface; particle-enhanced turbidimetric immunoassay; phosphate buffered saline; plasma rich in growth factors; platelet-derived growth factor; platelet-rich plasma; transforming growth factor-beta 1; variable fragment of immunoglogulins; vascular endothelial growth factor; wound healing

PMID:
24345372
DOI:
10.1016/j.exer.2013.12.005
[Indexed for MEDLINE]

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