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Aharoni, R., Department of Immunology, Weizmann Institute of Science, Rehovot, Israel
Kayhan, B., Department of Immunology, Weizmann Institute of Science, Rehovot, Israel
Brenner, O., Department of Veterinary Resources, Weizmann Institute of Science, Rehovot, Israel
Domev, H., Department of Immunology, Weizmann Institute of Science, Rehovot, Israel
Labunskay, G., Department of Immunology, Weizmann Institute of Science, Rehovot, Israel
Arnon, R., Department of Immunology, Weizmann Institute of Science, Rehovot, Israel, Department of Immunology, Weizmann Institute of Science, Rehovot, 76100, Israel
Inflammatory bowel disease (IBD) is characterized by detrimental immune reactivity in the gut and imbalance between proinflammatory and anti-inflammatory reactivity. In an attempt to down-regulate colitis, we investigated the effect of the immunomodulator glatiramer acetate (GA, Copaxone, copolymer 1) on two murine models of IBD, chemically induced and spontaneous. Acute experimental colitis of different levels of severity was induced in C57BL/6 mice by dextran sulfate sodium (DSS) administered orally at different concentrations and frequencies. It was manifested in weight loss, intestinal bleeding, and diarrhea, as well as by macroscopic and microscopic colon damage. GA treatment led to amelioration of all of these pathological manifestations, resulting in improved long-term survival. Moreover, even when colitis was induced by three cycles of DSS in this highly susceptible mouse strain, as well as in BALB/c mice that exhibit a chronic disease pattern, a substantial reduction in disease activity and mortality was obtained. GA treatment induced a beneficial effect also in a spontaneous model of colitis developed in the C3H/HeJBir IL-10-deficient mice. The detrimental proinflammatory response manifested by proliferation, tumor necrosis factor-α, and interferon-γ expression was modulated by GA, whereas the regulatory anti-inflammatory transforming growth factor-β and IL-10 cytokines response was elevated. This was demonstrated on the level of protein secretion in splenocytes and local mesenteric lymphocytes in response to syngeneic colon extract and in the overall response to anti-CD3, as well as on the level of mRNA expression in the colon. Copyright © 2006 by The American Society for Pharmacology and Experimental Therapeutics.
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Immunomodulatory therapeutic effect of glatiramer acetate on several murine models of inflammatory bowel disease
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Aharoni, R., Department of Immunology, Weizmann Institute of Science, Rehovot, Israel
Kayhan, B., Department of Immunology, Weizmann Institute of Science, Rehovot, Israel
Brenner, O., Department of Veterinary Resources, Weizmann Institute of Science, Rehovot, Israel
Domev, H., Department of Immunology, Weizmann Institute of Science, Rehovot, Israel
Labunskay, G., Department of Immunology, Weizmann Institute of Science, Rehovot, Israel
Arnon, R., Department of Immunology, Weizmann Institute of Science, Rehovot, Israel, Department of Immunology, Weizmann Institute of Science, Rehovot, 76100, Israel
Immunomodulatory therapeutic effect of glatiramer acetate on several murine models of inflammatory bowel disease
Inflammatory bowel disease (IBD) is characterized by detrimental immune reactivity in the gut and imbalance between proinflammatory and anti-inflammatory reactivity. In an attempt to down-regulate colitis, we investigated the effect of the immunomodulator glatiramer acetate (GA, Copaxone, copolymer 1) on two murine models of IBD, chemically induced and spontaneous. Acute experimental colitis of different levels of severity was induced in C57BL/6 mice by dextran sulfate sodium (DSS) administered orally at different concentrations and frequencies. It was manifested in weight loss, intestinal bleeding, and diarrhea, as well as by macroscopic and microscopic colon damage. GA treatment led to amelioration of all of these pathological manifestations, resulting in improved long-term survival. Moreover, even when colitis was induced by three cycles of DSS in this highly susceptible mouse strain, as well as in BALB/c mice that exhibit a chronic disease pattern, a substantial reduction in disease activity and mortality was obtained. GA treatment induced a beneficial effect also in a spontaneous model of colitis developed in the C3H/HeJBir IL-10-deficient mice. The detrimental proinflammatory response manifested by proliferation, tumor necrosis factor-α, and interferon-γ expression was modulated by GA, whereas the regulatory anti-inflammatory transforming growth factor-β and IL-10 cytokines response was elevated. This was demonstrated on the level of protein secretion in splenocytes and local mesenteric lymphocytes in response to syngeneic colon extract and in the overall response to anti-CD3, as well as on the level of mRNA expression in the colon. Copyright © 2006 by The American Society for Pharmacology and Experimental Therapeutics.
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