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用抗白细胞介素-4单克隆抗体进行治疗可阻断通过口服II型胶原对小鼠胶原诱导性关节炎的抑制作用。

Treatment with an anti-IL-4 monoclonal antibody blocks suppression of collagen-induced arthritis in mice by oral administration of type II collagen.

作者信息

Yoshino S

机构信息

Department of Microbiology, Saga Medical School, Japan.

出版信息

J Immunol. 1998 Mar 15;160(6):3067-71.

PMID:9510213
Abstract

Oral administration of type II collagen (CII) has been shown to suppress collagen-induced arthritis (CIA) in experimental animals. However, the exact mechanism by which CIA is suppressed following administration of CII remains to be investigated, although it was demonstrated that active suppression by regulatory T cells might be involved in the suppression. Therefore, we have examined whether the inhibitory cytokine IL-4 plays a role in the suppression of CIA, by using an anti-IL-4 mAb (11B11 mAb). Mice were fed daily with CII over a period of 10 days before immunization with CII. 11B11 mAb was i.p. injected 30 min before each oral administration of CII. The results showed that treatment with 11B11 mAb markedly blocked suppression of CIA by the oral Ag. The blockade of suppression of CIA by the anti-IL-4 mAb was associated with the blockade of augmentation of IL-4 secretion in CII-fed mice. The treatment with 11B11 mAb also resulted in the prevention of decreases in anti-CII IgG2a Ab production, DTH responses to CII, proliferation of lymphoid cells to CII, and IFN-gamma secretion in mice given CII orally. Thus, the neutralization of IL-4 by an anti-IL-4 Ab appears to be effective in blocking suppression of CIA by oral administration of CII, suggesting that IL-4 may be critically involved in its suppression.

摘要

口服II型胶原蛋白(CII)已被证明可在实验动物中抑制胶原蛋白诱导的关节炎(CIA)。然而,尽管已证明调节性T细胞的主动抑制可能参与其中,但CII给药后抑制CIA的确切机制仍有待研究。因此,我们通过使用抗IL-4单克隆抗体(11B11单克隆抗体)来研究抑制性细胞因子IL-4是否在CIA的抑制中起作用。在用CII免疫前10天,每天给小鼠喂食CII。在每次口服CII前30分钟腹腔注射11B11单克隆抗体。结果表明,用11B11单克隆抗体处理显著阻断了口服抗原对CIA的抑制作用。抗IL-4单克隆抗体对CIA抑制作用的阻断与CII喂养小鼠中IL-4分泌增加的阻断相关。用11B11单克隆抗体处理还导致口服CII的小鼠中抗CII IgG2a抗体产生的减少、对CII的迟发型超敏反应、淋巴细胞对CII的增殖以及IFN-γ分泌的预防。因此,抗IL-4抗体对IL-4的中和似乎有效地阻断了口服CII对CIA的抑制作用,表明IL-4可能在其抑制中起关键作用。

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Treatment with an anti-IL-4 monoclonal antibody blocks suppression of collagen-induced arthritis in mice by oral administration of type II collagen.用抗白细胞介素-4单克隆抗体进行治疗可阻断通过口服II型胶原对小鼠胶原诱导性关节炎的抑制作用。
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引用本文的文献

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Prenatal exposure to bisphenol A up-regulates immune responses, including T helper 1 and T helper 2 responses, in mice.在小鼠中,孕期暴露于双酚A会上调免疫反应,包括辅助性T细胞1型和辅助性T细胞2型反应。
Immunology. 2004 Jul;112(3):489-95. doi: 10.1111/j.1365-2567.2004.01900.x.
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Oral administration of type II collagen suppresses pro-inflammatory mediator production by synoviocytes in rats with adjuvant arthritis.口服II型胶原蛋白可抑制佐剂性关节炎大鼠滑膜细胞促炎介质的产生。
Clin Exp Immunol. 2003 Jun;132(3):416-23. doi: 10.1046/j.1365-2249.2003.02167.x.
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Effects of bisphenol A on antigen-specific antibody production, proliferative responses of lymphoid cells, and TH1 and TH2 immune responses in mice.
双酚A对小鼠抗原特异性抗体产生、淋巴细胞增殖反应以及TH1和TH2免疫反应的影响。
Br J Pharmacol. 2003 Apr;138(7):1271-6. doi: 10.1038/sj.bjp.0705166.
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Bacterial lipopolysaccharide acts as an adjuvant to induce autoimmune arthritis in mice.细菌脂多糖作为佐剂可诱导小鼠患自身免疫性关节炎。
Immunology. 2000 Apr;99(4):607-14. doi: 10.1046/j.1365-2567.2000.00015.x.
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The role of lipopolysaccharide injected systemically in the reactivation of collagen-induced arthritis in mice.全身注射脂多糖在小鼠胶原诱导性关节炎再激活中的作用。
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