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Blood, 15 December 2005, Vol. 106, No. 13, pp. 4351-4358.
Prepublished online as a Blood First Edition Paper on August 23, 2005; DOI 10.1182/blood-2005-03-1029.


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PHAGOCYTES

1{alpha},25-dihydroxyvitamin D3 is a potent suppressor of interferon {gamma}–mediated macrophage activation

Laura Helming, Jens Böse, Jan Ehrchen, Stefanie Schiebe, Thomas Frahm, Robert Geffers, Michael Probst-Kepper, Rudi Balling, and Andreas Lengeling

From the Junior Research Group Infection Genetics, German Research Centre for Biotechnology, Braunschweig, Germany; Institute for Experimental Dermatology, University of Münster, Münster, Germany; Department of Gene Regulation and Differentiation, German Research Centre for Biotechnology, Braunschweig, Germany; Research Group Mucosal Immunity, German Research Centre for Biotechnology, Braunschweig, Germany; German Research Centre for Biotechnology, Braunschweig, Germany; and Department of Visceral and Transplant Surgery, Hannover Medical School, Hannover, Germany.

1{alpha},25-dihydroxyvitamin D3 (1{alpha},25(OH)2D3), the activated vitamin D3 hormone, is a key regulator of calcium homeostasis and thereby indispensable for bone metabolism. In addition, 1{alpha},25(OH)2D3 is known to mediate predominantly immunosuppressive responses in vitro and in vivo. It has been demonstrated that macrophages can produce 1{alpha},25(OH)2D3 on activation with interferon {gamma} (IFN-{gamma}), although little is understood about the biologic significance of this response. We show here that 1{alpha},25(OH)2D3 can selectively suppress key effector functions of IFN-{gamma}–activated macrophages. Among these are the suppression of listericidal activity, the inhibition of phagocyte oxidase-mediated oxidative burst, and the suppression of important IFN-{gamma}–induced genes, including Ccl5, Cxcl10, Cxcl9, Irf2, Fcgr1, Fcgr3, and Tlr2. The deactivation of IFN-{gamma}–stimulated macrophages is dependent on a functional vitamin D receptor and 1{alpha},25(OH)2D3 acts specifically on IFN-{gamma}–activated macrophages, whereas the steroid has no effects on resting macrophages. Therefore, the 1{alpha},25(OH)2D3–mediated suppression of macrophage functions is distinct from previously described macrophage deactivation mechanisms. In conclusion, our data indicate that the production of 1{alpha},25(OH)2D3 by IFN-{gamma}–stimulated macrophages might be an important negative feedback mechanism to control innate and inflammatory responses of activated macrophages.


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