Pretreatment with Interferon-γ Enhances the Therapeutic Activity of Mesenchymal Stromal Cells in Animal Models of Colitis

Author:

Duijvestein Marjolijn1,Wildenberg Manon E.12,Welling Mick M.3,Hennink Simone1,Molendijk Ilse1,van Zuylen Vanessa L.4,Bosse Tjalling5,Vos Anne Christine W.1,de Jonge-Muller Eveline S. M.1,Roelofs Helene4,van der Weerd Louise36,Verspaget Hein W.1,Fibbe Willem E.4,te Velde Anje A.7,van den Brink Gijs R.12,Hommes Daniel W.1

Affiliation:

1. Department of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands

2. Tytgat Institute for Liver and Intestinal ResearchAmsterdam, The Netherlands

3. Division of Nuclear Medicine, Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands

4. Department of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, The Netherlands

5. Department of Pathology, Leiden University Medical Center, Leiden, The Netherlands

6. Department of Anatomy & Embryology, Leiden University Medical Center, Leiden, The Netherlands

7. Center for Experimental and Molecular Medicine, Academic Medical Center, Amsterdam, The Netherlands

Abstract

Abstract Mesenchymal stromal cells (MSCs) are currently under investigation for the treatment of inflammatory disorders, including Crohn's disease. MSCs are pluripotent cells with immunosuppressive properties. Recent data suggest that resting MSCs do not have significant immunomodulatory activity, but that the immunosuppressive function of MSCs has to be elicited by interferon-γ (IFN-γ). In this article, we assessed the effects of IFN-γ prestimulation of MSCs (IMSCs) on their immunosuppressive properties in vitro and in vivo. To this end, we pretreated MSCs with IFN-γ and assessed their therapeutic effects in dextran sodium sulfate (DSS)- and trinitrobenzene sulfonate (TNBS)-induced colitis in mice. We found that mice treated with IMSCs (but not MSCs) showed a significantly attenuated development of DSS-induced colitis. Furthermore, IMSCs alleviated symptoms of TNBS-induced colitis. IMSC-treated mice displayed an increase in body weight, lower colitis scores, and better survival rates compared with untreated mice. In addition, serum amyloid A protein levels and local proinflammatory cytokine levels in colonic tissues were significantly suppressed after administration of IMSC. We also observed that IMSCs showed greater migration potential than unstimulated MSCs to sites within the inflamed intestine. In conclusion, we show that prestimulation of MSCs with IFN-γ enhances their capacity to inhibit Th1 inflammatory responses, resulting in diminished mucosal damage in experimental colitis. These data demonstrate that IFN-γ activation of MSCs increases their immunosuppresive capacities and importantly, their therapeutic efficacy in vivo.

Funder

Dutch Digestive Foundation

MLDS

Digest Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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