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DOI: 10.1055/s-2006-947240
© Georg Thieme Verlag KG Stuttgart · New York
The Effects of Triptolide on Enteric Mucosal Immune Responses of DBA/1 Mice with Collagen-Induced Arthritis
Publikationsverlauf
Received: April 3, 2006
Accepted: July 11, 2006
Publikationsdatum:
18. September 2006 (online)
Abstract
For investigating the effects of triptolide on enteric mucosal immune responses of DBA/1 mice with collagen-induced arthritis (CIA), the changes of the Peyer’s patches, IEL (intraepithelial lymphocytes), LPL (lamina propria lymphocytes), periphery lymphocytes, and levels of TGF-β in CIA mice were checked with flow cytometry or ELISA. Our results showed that triptolide could lower the arthritic scores and increase TGF-β level. Triptolide also had an effect on enteric mucosal immune lymphocytes in Peyer’s patch, IEL and LPL of CIA mice. The regulation of enteric mucosal lymphocytes might explain some of the immunosuppressive activities of triptolide.
Key words
Triptolide - Peyer’s patch - IEL - LPL - collagen-induced arthritis
References
- 1 Tao X, Davis L S, Lipsky P E. Effect of an extract of the Chinese herbal remedy Tripterygium wilfordii Hook F on human immune responsiveness. Arthritis Rheum. 1991; 34 1274-81
- 2 Gu W Z, Chen R, Brandwein S, McAlpine J, Burres N. Isolation, purification, and characterization of immunosuppressive compounds from Tripterygium: triptolide and tripdiolide. Int J Immunopharmacol. 1995; 17 351-6
- 3 Hu K B, Liu Z H, Liu D, Li L S. Inhibition of vascular endothelial growth factor expression and production by triptolide. Planta Med. 2002; 68 368-9
- 4 Qiu D, Kao P N. Immunosuppressive and anti-inflammatory mechanisms of triptolide, the principal active diterpenoid from the Chinese medical herb Tripterygium wilfordii Hook F. Drug R D. 2003; 4 1-18
- 5 Zhu K J, Shen Q Y, Cheng H, Mao X H, Lao L M, Hao L L. Triptolide affects the differentiation, maturation and function of human dendritic cells. Int Immunopharmacol. 2005; 5 1415-26
- 6 Kim W U, Lee W K, Ryoo J W, Kim S H, Kim J, Youn J. et al . Suppression of collagen-induced arthritis by single administration of poly (lactic-co-glycolic acid) nanoparticles entrapping type II collagen: a novel treatment strategy for induction of oral tolerance. Arthritis Rheum. 2002; 46 1109-20
- 7 Haqqi T M, David C S. T-cell receptor V beta genes repertoire in mice. Possible role in resistance and susceptibility to type II collagen-induced arthritis. J Autoimmun. 1990; 3 113-21
- 8 Holmdahl R, Rubin K, Klareskog L, Larsson E, Wigzell H. Characterization of the antibody response in mice with type II collagen-induced arthritis, using monoclonal anti-type II collagen antibodies. Arthritis Rheum. 1986; 29 400-10
- 9 Svendsen P, Andersen C B, Willcox N, Coyle A J, Holmdahl R, Kamradt T. et al . Tracking of proinflammatory collagen-specific T cells in early and late collagen-induced arthritis in humanized mice. J Immunol. 2004; 173 7037-45
- 10 Holmdahl R, Jansson L, Meyerson B, Klareskog L. Oestrogen induced suppression of collagen arthritis: I. Long term oestradiol treatment of DBA/1 mice reduces severity and incidence of arthritis and decreases the anti type II collagen immune response. Clin Exp Immunol. 1987; 70 372-8
- 11 Zhou J, Xiao C, Zhao L, Jia H, Zhao N, Lu C. et al . The effect of triptolide on CD4+ and CD8+ cells in Peyer’s patch of SD rats with collagen induced arthritis. Int Immunopharmacol. 2006; 6 98-203
- 12 Lyscom N, Brueton M J. Intraepithelial, lamina propria and Peyer’s patch lymphocytes of the rat small intestine: isolation and characterization in terms of immunoglobulin markers and receptors for monoclonal antibodies. Immunology. 1982; 45 775-83
- 13 Mosley R L, Klein J R. A rapid method for isolating murine intestine intraepithelial lymphocytes with high yield and purity. J Immunol Methods. 1992; 156 19-26
- 14 Yuan Q, Walker W A. Innate immunity of the gut: mucosal defense in health and disease. J Pediatr Gastroenterol Nutr. 2004; 38 463-73
- 15 Kiyono H, Fukuyama S. NALT-versus Peyer's-patch-mediated mucosal immunity. Nat Rev Immunol. 2004; 4 699-710
- 16 Erickson K L, Hubbard N E. Probiotic immunomodulation in health and disease. J Nutr. 2000; 130 403-9
- 17 Guy-Grand D, Vassalli P. Gut intraepithelial lymphocyte development. Curr Opin Immunol. 2002; 14 255-9
- 18 Heel K A, McCauley R D, Papadimitriou J M, Hall J C. Review: Peyer’s patches. J Gastroenterol Hepatol. 1997; 12 122-36
- 19 Yoshikai Y. The interaction of intestinal epithelial cells and intraepithelial lymphocytes in host defense. Immunol Res. 1999; 20 219-35
- 20 Henschke S, Pawlowski N N, Wild M K, Kroesen A J, Zeitz M, Hoffmann J C. Lamina propria T cell activation: role of the costimulatory molecule CD2 and its cytoplasmic tail for the regulation of proliferation and apoptosis. Int J Colorectal Dis. 2005; 23 1-11
- 21 Di Leo V, D'Inca R, Bettini M B, Podswiadek M, Punzi L, Mastropaolo G. et al . Effect of Helicobacter pylori and eradication therapy on gastrointestinal permeability. Implications for patients with seronegative spondyloarthritis. J Rheumatol. 2005; 32 295-300
- 22 Salmi M, Jalkanen S. Human leukocyte subpopulations from inflamed gut bind to joint vasculature using distinct sets of adhesion molecules. J Immunol. 2001; 166 4650-7
- 23 Salmi M, Jalkanen S. Human leukocyte subpopulations from inflamed gut bind to joint vasculature using distinct sets of adhesion molecules. Int Immunol. 2003; 15 145-58
- 24 Toivanen P. Normal intestinal microbiota in the aetiopathogenesis of rheumatoid arthritis. Annal Rheum Dis. 2003; 62 807-11
- 25 Asano K, Matsuishi J, Yu Y, Kasahara T, Hisamitsu T. Suppressive effects of Tripterygium wilfordii Hook F, a traditional Chinese medicine, on collagen arthritis in mice. Immunopharmacology. 1998; 39 117-26
Prof. Dr. Aiping Lu
Institute of Basic Theory
China Academy of Traditional Chinese Medicine
Dongzhimen
Beijing 100700
People’s Republic of China
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