An acidic polysaccharide of Panax ginseng ameliorates experimental autoimmune encephalomyelitis and induces regulatory T cells

被引:84
作者
Hwang, Insun [1 ,2 ]
Ahn, Ginnae [1 ,2 ]
Park, Eunjin [1 ,2 ]
Ha, Danbee [1 ,2 ]
Song, Jie-Young [3 ]
Jee, Youngheun [1 ,2 ]
机构
[1] Jeju Natl Univ, Coll Vet Med, Cheju, South Korea
[2] Jeju Natl Univ, Appl Radiol Inst, Cheju, South Korea
[3] Korea Inst Radiol & Med Sci, Immunol Lab, Seoul, South Korea
关键词
Acidic polysaccharide; Panax ginseng; Experimental autoimmune encephalomyelitis (EAE); Central nervous system (CNS); MULTIPLE-SCLEROSIS; GLATIRAMER ACETATE; POTENT ADJUVANTS; DISEASE; INFLAMMATION; T(H)17; TLR4; BETA; DIFFERENTIATION; ACTIVATION;
D O I
10.1016/j.imlet.2011.04.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
An acidic polysaccharide of Panax ginseng (APG), so called ginsan, is a purified polysaccharide. APG has multiple immunomodulatory effects of stimulating natural killer (NK) and T cells and producing a variety of cytokines that proved to diminish the proinflammatory response, and protect from septic lethality. To determine APG's role in the autoimmune demyelinating disease, we tested whether APG can regulate inflammatory and encephalitogenic response in experimental autoimmune encephalomyelitis (EAE), an animal model of human multiple sclerosis (MS). Here, we demonstrate the therapeutic efficacy of the APG which induces the suppression of an encephalitogenic response during EAE. APG significantly ameliorates the progression of EAE by inhibiting the proliferation of autoreactive T cells and the production of inflammatory cytokines such as IFN-gamma, IL-1 beta and IL-17. More importantly, APG promotes the generation of immunosuppressive regulatory T cells (Tregs) through the activation of transcription factor, Foxp3. Furthermore, the depletion of CD25(+) cells from APG-treated EAE mice abrogates the beneficial effects of EAE. The capacity of APG to induce clinically beneficial effects furthers our understanding of the basis for its therapeutic immunosuppression of EAE and, possibly, MS. Thus, our results suggest that APG may serve as an effective therapy for MS and other autoimmune diseases. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:169 / 178
页数:10
相关论文
共 33 条
[1]
Protection of Staphylococcus aureus-infected septic mice by suppression of early acute inflammation and enhanced antimicrobial activity by ginsan [J].
Ahn, JY ;
Song, JY ;
Yun, YS ;
Jeong, GJ ;
Choi, IS .
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, 2006, 46 (02) :187-197
[2]
Reciprocal developmental pathways for the generation of pathogenic effector TH17 and regulatory T cells [J].
Bettelli, E ;
Carrier, YJ ;
Gao, WD ;
Korn, T ;
Strom, TB ;
Oukka, M ;
Weiner, HL ;
Kuchroo, VK .
NATURE, 2006, 441 (7090) :235-238
[3]
Intra-articularly localized bacterial DNA containing CpG motifs induces arthritis [J].
Deng, GM ;
Nilsson, IM ;
Verdrengh, M ;
Collins, LV ;
Tarkowski, A .
NATURE MEDICINE, 1999, 5 (06) :702-705
[4]
Loxoribine, a selective Toll-like receptor 7 agonist, induces maturation of human monocyte-derived dendritic cells and stimulates their Th-1-and Th-17-polarizing capability [J].
Dzopalic, Tanja ;
Dragicevic, Ana ;
Vasilijic, Sasa ;
Vucevic, Dragana ;
Majstorovic, Ivana ;
Bozic, Biljana ;
Balint, Bela ;
Colic, Miodrag .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2010, 10 (11) :1428-1433
[5]
Vasoactive intestinal peptide induces regulatory T cells during experimental autoimmune encephalomyelitis [J].
Fernandez-Martin, A ;
Gonzalez-Rey, E ;
Chorny, A ;
Ganea, D ;
Delgado, M .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2006, 36 (02) :318-326
[6]
Foxp3 Programs the Development and Function of CD4+CD25+ Regulatory T Cells (Reprinted from vol 4, pg 330-336, 2003) [J].
Fontenot, Jason D. ;
Gavin, Marc A. ;
Rudensky, Alexander Y. .
JOURNAL OF IMMUNOLOGY, 2017, 198 (03) :986-992
[7]
Multiple toll-like receptor agonists act as potent adjuvants in the induction of autoimmunity [J].
Hansen, BS ;
Hussain, RZ ;
Lovett-Racke, AE ;
Thomas, JA ;
Racke, MK .
JOURNAL OF NEUROIMMUNOLOGY, 2006, 172 (1-2) :94-103
[8]
Control of regulatory T cell development by the transcription factor Foxp3 [J].
Hori, S ;
Nomura, T ;
Sakaguchi, S .
SCIENCE, 2003, 299 (5609) :1057-1061
[9]
CD4+CD25+ regulatory T cells contribute to the therapeutic effects of glatiramer acetate in experimental autoimmune encephalomyelitis [J].
Jee, Y. ;
Piao, W. H. ;
Liu, R. ;
Bai, X. F. ;
Rhodes, S. ;
Rodebaugh, R. ;
Campagnolo, D. I. ;
Shi, F. D. ;
Vollmer, T. L. .
CLINICAL IMMUNOLOGY, 2007, 125 (01) :34-42
[10]
Preferential Recruitment of Interferon-γ-Expressing TH17 Cells in Multiple Sclerosis [J].
Kebir, Hania ;
Ifergan, Igal ;
Alvarez, Jorge Ivan ;
Bernard, Monique ;
Poirier, Josee ;
Arbour, Nathalie ;
Duquette, Pierre ;
Prat, Alexandre .
ANNALS OF NEUROLOGY, 2009, 66 (03) :390-402