食品科学 ›› 2009, Vol. 30 ›› Issue (17 ): 297-301.doi: 10.7506/spkx1002-6630-200917069

• 营养卫生 • 上一篇    下一篇

牛初乳中的IgG 对肠黏膜免疫系统调节的初步研究

李 杨,庞广昌* ,于立琴   

  1. 天津市食品生物技术重点实验室,天津商业大学生物技术与食品科学学院
  • 收稿日期:2009-06-08 出版日期:2009-09-01 发布日期:2014-04-14
  • 通讯作者: 庞广昌* E-mail:pgc@tjcu.edu.cn
  • 基金资助:

    国家自然科学基金项目(30871951)

Regulatory Effects of IgG from Bovine Colostrum on Gastrointestinal Mucosa Immunity System

LI Yang,PANG Guang-chang*,YU Li-qin   

  1. Tianjin Key Laboratory of Food Biotechnology, College of Biotechnology and Food Science, Tianjin University of Commerce,
    Tianjin 300134, China
  • Received:2009-06-08 Online:2009-09-01 Published:2014-04-14
  • Contact: PANG Guang-chang*, E-mail:pgc@tjcu.edu.cn

摘要:

目的:探索牛初乳中的IgG 对家兔胃肠黏膜免疫系统中细胞因子网络的调节作用。方法:以家兔为研究对象,通过口服,腹腔注射,耳静脉注射IgG 这三种给药方式,分别在3、2、2h 后取血,并用ELISA 法检测血清中IFN-γ,TNF- α,TGF-β1,IL-1β,IL-10,IL-4,IL-6,IL-1Ra 的水平。结果:口服IgG 后发炎细胞因子IL-6,IL-1β,TNF-α,IFN-γ水平比给药前显著上升,抗炎细胞因子IL-1Ra、IL-4、IL-10 及TGF-β1 的水平比给药前显著下降;而腹腔注射和静脉注射IgG 后,抗炎细胞因子水平升高,发炎细胞因子水平下降。结论:口服牛初乳中的IgG,IgG 并不会被吸收,而是被肠上皮细胞、巨噬细胞、肥大细胞以及NK 细胞等先天免疫细胞所识别,并最终促进发炎细胞因子的产生,抑制抗炎细胞因子的产生。相反,腹腔和静脉注射IgG,IgG会与免疫细胞的FcγR Ⅱ B 受体结合,从而抑制发炎细胞因子的产生,诱导抗炎细胞因子的产生。

关键词: 牛初乳, IgG, 细胞因子, 肠黏膜免疫系统

Abstract:

Objective: To explore and evaluate the regulatory effects of IgG from bovine colostrum on cytokine network in gastrointestinal mucoca immunity system. Methods: Rabbit serum was collected 3, 2, and 2 h after oral administration, intraperitoneal injection and ear intravenous injection with IGF-1, respectively, to examine the contents of IFN-γ, TNF-α, TGF-β1, IL-1β, IL-10, IL-4, IL-6 and IL-1Ra by ELISA assay. Results: After oral administration, the contents of inflammatory cytokines like IFN-γ, IL-6, IL-1 and TNF-α were significantly increased while those of anti-inflammatory cytokines like TGF-β1, IL-10, IL-4 and IL-1Ra were significantly decreased. The IgG administration by intraperitoneal injection or ear intravenous injection resulted in the content increases of the anti-inflammatory cytokines and the content decrease of the inflammatory cytokines. Conclusions: IgG which is administered orally can not be absorbed but identified easily by intestinal epithelial cells, macrophages, mast cells, NK cells and other innate immune cells and thus induces the production of inflammatory cytokines and inhibits the production of anti-inflammatory cytokines. In contrast, IgG administered in the ways of intraperitoneal injection and intravenous injection is easy to bind with the inhibitory FcγR Ⅱ B of immune cells so as to inhibit the production of inflammatory cytokines and induce the production of anti-inflammatory cytokines.

Key words: bovine colostrum, IgG, cytokine, gastrointestinal mucosa immunity system

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