Combination of IL-2, rapamycin, DNA methyltransferase and histone deacetylase inhibitors for the expansion of human regulatory T cells
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Makoto Miyara1,2, Driss Chader1,2, Aude Burlion2, Jérémie Goldstein2, Delphine Sterlin1,2, Françoise Norol3, Hélène Trebeden-Nègre3, Laetitia Claër1,2, Shimon Sakaguchi4,*, Gilles Marodon2,*, Zahir Amoura1,2,5,6,* and Guy Gorochov1,2,6
1 Department of immunology, AP-HP Pitié Salpêtrière, Paris, France
2 Sorbonne Universités, UPMC Univ Paris 06, INSERM, CNRS, Centre d’Immunologie et des Maladies Infectieuses (CIMI-Paris), Paris, France
3 Cell Therapy, AP-HP Pitié Salpêtrière, Paris, France
4 Experimental Immunology, Immunology Frontier Research Center, Osaka University, Osaka, Japan
5 Internal Medicine, French Reference Center for Systemic Lupus Erythematosus and Antiphospholipid Syndrome, AP-HP Pitié Salpêtrière, Paris, France
6 UPMC Paris Sorbonne, Paris, France
* These authors have contributed equally to this work
Makoto Miyara, email:
Guy Gorochov, email:
Keywords: human regulatory T cells, FOXP3, cell therapy, autoimmunity, GVH
Received: June 07, 2016 Accepted: June 09, 2016 Published: July 28, 2016
FOXP3+ regulatory T cell (Treg) based cellular therapies represent promising therapeutic options in autoimmunity, allergy, transplantation and prevention of Graft Versus Host (GVH) Disease. Among human FOXP3-expressing CD4+T cells, only the CD45RA+ naïve Treg (nTreg) subset is suitable for in vitro expansion. However, FOXP3 expression decays in cells using currently described culture protocols.
Rapamycin alone was not able to prevent FOXP3 loss in nTregs cells, as only a half of them maintained FOXP3 expression after 14 days of culture. In contrast we report a novel combined drug regimen that can drastically stabilize FOXP3 expression in cultured Tregs. IL-2, rapamycin, histone deacetylase and DNA methyltransferase inhibitors act in synergy to allow expansion of human regulatory T cells with sustained high expression of FOXP3 and CD15s with potent suppressive capacities in vitro and control of murine xeno-GVH reactions. Of note, an additional subsequent infusion of expanded nTreg cells did not improve survival of mice.
Combination of IL-2, rapamycin, histone deacetylase and DNA methyltransferase inhibitors is optimal for the expansion in vitro of pure effective nTreg maintaining high levels of FOXP3 for therapeutic purposes.
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