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

被引:323
作者
Duijvestein, Marjolijn [1 ]
Wildenberg, Manon E. [1 ,6 ]
Welling, Mick M. [2 ]
Hennink, Simone [1 ]
Molendijk, Ilse [1 ]
van Zuylen, Vanessa L. [3 ]
Bosse, Tjalling [4 ]
Vos, Anne Christine W. [1 ]
de Jonge-Muller, Eveline S. M. [1 ]
Roelofs, Helene [3 ]
van der Weerd, Louise [2 ,5 ]
Verspaget, Hein W. [1 ]
Fibbe, Willem E. [3 ]
Velde, Anje A. Te [7 ]
van den Brink, Gijs R. [1 ,6 ]
Hommes, Daniel W. [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Gastroenterol & Hepatol, NL-2333 ZA Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Div Nucl Med, Dept Radiol, NL-2333 ZA Leiden, Netherlands
[3] Leiden Univ, Med Ctr, Dept Immunohematol & Blood Transfus, NL-2333 ZA Leiden, Netherlands
[4] Leiden Univ, Med Ctr, Dept Pathol, NL-2333 ZA Leiden, Netherlands
[5] Leiden Univ, Med Ctr, Dept Anat & Embryol, NL-2333 ZA Leiden, Netherlands
[6] Univ Amsterdam, Acad Med Ctr, Tytgat Inst Liver & Intestinal Res, NL-1105 AZ Amsterdam, Netherlands
[7] Univ Amsterdam, Acad Med Ctr, Ctr Expt & Mol Med, NL-1105 AZ Amsterdam, Netherlands
关键词
Crohn's disease; Mesenchymal stem cell; Mesenchymal stromal cells; Experimental mouse model; STEM-CELLS; IFN-GAMMA; MURINE; RESPONSES; RECOVERY; INHIBIT; TISSUES; FAILURE; FISTULA; DISEASE;
D O I
10.1002/stem.698
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
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-gamma (IFN-gamma). In this article, we assessed the effects of IFN-gamma prestimulation of MSCs (IMSCs) on their immunosuppressive properties in vitro and in vivo. To this end, we pretreated MSCs with IFN-gamma 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-gamma enhances their capacity to inhibit Th1 inflammatory responses, resulting in diminished mucosal damage in experimental colitis. These data demonstrate that IFN-gamma activation of MSCs increases their immunosuppresive capacities and importantly, their therapeutic efficacy in vivo. STEM CELLS 2011;29:1549-1558
引用
收藏
页码:1549 / 1558
页数:10
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