Concise review: Combining human leukocyte antigen G and mesenchymal stem cells for immunosuppressant biotherapy

Author:

Naji Abderrahim1,Rouas-Freiss Nathalie12,Durrbach Antoine34,Carosella Edgardo D.12,Sensébé Luc5,Deschaseaux Frédéric5

Affiliation:

1. CEA, Institut des Maladies Emergentes et des Therapies Innovantes (IMETI) Service de Recherche en Hemato-Immunologie (SRHI), Hopital Saint-Louis, Paris, France

2. Univ Paris Diderot Sorbonne Paris Cité, IUH, Hopital Saint-LouisUMR_E5, Paris, France

3. INSERM U1014, Villejuif, France

4. Département de Néphrologie Université Paris XI, Hôpital du Kremlin-Bicêtre, IFRNT, Le Kremlin-Bicêtre, France

5. Stromalab UMR CNRS 5273, U1031 Inserm EFS-Pyrénées-Méditerranée, University P. Sabatier, Toulouse, France

Abstract

Abstract Both human leukocyte antigen G (HLA-G) and multipotential mesenchymal stem/stromal cells (MSCs) exhibit immunomodulatory functions. In allogeneic tranplantation, the risks of acute and chronic rejection are still high despite improvement in immunosuppressive treatments, and the induction of a state of tolerance to alloantigens is not achieved. Immunomodulatory properties of MSCs and HLA-G in human allogeneic tranplantation to induce tolerance appears attractive and promising. Interestingly, we and others have demonstrated that MSCs can express HLA-G. In this review, we focus on the expression of HLA-G by MSCs and discuss how to ensure and improve the immunomodulatory properties of MSCs by selectively targeting MSCs expressing HLA-G (MSCsHLA-G+). We also discuss the possible uses of MSCsHLA-G+ for therapeutic purposes, notably, to overcome acute and chronic immune rejection in solid-organ allogeneic transplantation in humans. Since MSCs are phenotypically and functionally heterogeneous, it is of primary interest to have specific markers ensuring that they have strong immunosuppressive potential and HLA-G may be a valuable candidate.

Funder

Agence Nationale de la Recherche Technologies pour la Santé et l'Autonomie, a grant from the ATOS Project

European Commission FP7

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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