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The journal of immunology : official journal of the American Association of Immunologists v.197 no.8, 2016년, pp.2992 - 3007   SCI SCIE
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IFN-β Facilitates Neuroantigen-Dependent Induction of CD25+ FOXP3+ Regulatory T Cells That Suppress Experimental Autoimmune Encephalomyelitis

Wang, Duncheng (Department of Microbiology and Immunology, Brody School of Medicine, East Carolina University, Greenville, NC 27834 ) ; Ghosh, Debjani (and ) ; Islam, S. M. Touhidul (Department of Microbiology and Immunology, Brody School of Medicine, East Carolina University, Greenville, NC 27834 ) ; Moorman, Cody D. (and ) ; Thomason, Ashton E. (Department of Microbiology and Immunology, Brody School of Medicine, East Carolina University, Greenville, NC 27834 ) ; Wilkinson, Daniel S. (and ) ; Mannie, Mark D. (Department of Microbiology and Immunology, Brody School of Medicine, East Carolina University, Greenville, NC 27834 ) ;
  • 초록  

    This study introduces a flexible format for tolerogenic vaccination that incorporates IFN-β and neuroantigen (NAg) in the Alum adjuvant. Tolerogenic vaccination required all three components, IFN-β, NAg, and Alum, for inhibition of experimental autoimmune encephalomyelitis (EAE) and induction of tolerance. Vaccination with IFN-β + NAg in Alum ameliorated NAg-specific sensitization and inhibited EAE in C57BL/6 mice in pretreatment and therapeutic regimens. Tolerance induction was specific for the tolerogenic vaccine Ag PLP178-191 or myelin oligodendrocyte glycoprotein (MOG)35–55 in proteolipid protein– and MOG-induced models of EAE, respectively, and was abrogated by pretreatment with a depleting anti-CD25 mAb. IFN-β/Alum–based vaccination exhibited hallmarks of infectious tolerance, because IFN-β + OVA in Alum–specific vaccination inhibited EAE elicited by OVA + MOG in CFA but not EAE elicited by MOG in CFA. IFN-β + NAg in Alum vaccination elicited elevated numbers and percentages of FOXP3 + T cells in blood and secondary lymphoid organs in 2D2 MOG-specific transgenic mice, and repeated boosters facilitated generation of activated CD44 high CD25 + regulatory T cell (Treg) populations. IFN-β and MOG35–55 elicited suppressive FOXP3 + Tregs in vitro in the absence of Alum via a mechanism that was neutralized by anti–TGF-β and that resulted in the induction of an effector CD69 + CTLA-4 + IFNAR + FOXP3 + Treg subset. In vitro IFN-β + MOG–induced Tregs inhibited EAE when transferred into actively challenged recipients. Unlike IFN-β + NAg in Alum vaccines, vaccination with TGF-β + MOG35-55 in Alum did not increase Treg percentages in vivo. Overall, this study indicates that IFN-β + NAg in Alum vaccination elicits NAg-specific, suppressive CD25 + Tregs that inhibit CNS autoimmune disease. Thus, IFN-β has the activity spectrum that drives selective responses of suppressive FOXP3 + Tregs.


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