Immunogenicity and Immunomodulatory Properties of Umbilical Cord Lining Mesenchymal Stem Cells

Author:

Deuse Tobias123,Stubbendorff Mandy2,Tang-Quan Karis23,Phillips Neil4,Kay Mark A.4,Eiermann Thomas5,Phan Thang T.67,Volk Hans-Dieter8,Reichenspurner Hermann12,Robbins Robert C.3,Schrepfer Sonja123

Affiliation:

1. Cardiovascular Surgery, University Heart Center Hamburg, Hamburg, Germany

2. TSI-lab, Cardiovascular Research Center, University Hospital Hamburg-Eppendorf, Hamburg, Germany

3. Cardiothoracic Surgery, Stanford University School of Medicine, Standord, CA, USA

4. Pediatrics, Human Gene Therapy, Stanford University School of Medicine, Stanford, CA, USA

5. Transfusion Medicine, HLA-Lab, University Hospital Hamburg-Eppendorf, Hamburg, Germany

6. Surgery, Yong Loo Lin School of Medicine, Singapore

7. CellResearchCorp, Clinical Research Centre, Singapore

8. BCRT, Charite, Campus Virchow-Klinikum, Berlin, Germany

Abstract

We here present an immunologic head-to-head comparison between human umbilical cord lining mesenchymal stem cells (clMSCs) and adult bone marrow MSCs (bmMSCs) from patients >65 years of age. clMSCs had significantly lower HLA class I expression, higher production of tolerogenic TGF-β and IL-10, and showed significantly faster proliferation. In vitro activation of allogeneic lymphocytes and xenogeneic in vivo immune activation was significantly stronger with bmMSCs, whereas immune recognition of clMSCs was significantly weaker. Thus, bmMSCs were more quickly rejected in immunocompetent mice. IFN-γ at 25 ng/ml increased both immunogenicity by upregulation of HLA class I/HLA-DR expression and tolerogenicity by increasing intracellular HLA-G and surface HLA-E expression, augmenting TGF-β and IL-10 release, and inducing indoleamine 2,3-dioxygenase (IDO) expression. Higher concentrations of IFN-γ (>50 ng/ml) further enhanced the immunosuppressive phenotype of clMSCs, more strongly downregulating HLA-DR expression and further increasing IDO production (at 500 ng/ml). The net functional immunosuppressive efficacy of MSCs was tested in mixed lymphocyte cultures. Although both clMSCs and bmMSCs significantly reduced in vitro immune activation, clMSCs were significantly more effective than bmMSCs. The veto function of both MSC lines was enhanced in escalating IFN-γ environments. In conclusion, clMSCs show a more beneficial immunogeneic profile and stronger overall immunosuppressive potential than aged bmMSCs.

Publisher

SAGE Publications

Subject

Transplantation,Cell Biology,Biomedical Engineering

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