Kline J N, Krieg A M, Waldschmidt T J, Ballas Z K, Jain V, Businga T R
Departments of Medicine and Pathology, University of Iowa College of Medicine, Iowa City, USA.
J Allergy Clin Immunol. 1999 Dec;104(6):1258-64. doi: 10.1016/s0091-6749(99)70022-9.
Oligodeoxynucleotides (ODNs) containing the dinucleotide CpG in a specific sequence context (CpG-ODNs) have the ability to prevent the development of eosinophilic airway inflammation and bronchial hyperreactivity in a murine model of asthma. We have previously demonstrated that CpG-ODNs stimulate expression of the T(H1)-inducing cytokines IFN-gamma and IL-12 in a murine model of asthma and that this stimulation is associated with the protection against asthmatic inflammation.
The purpose of this study was to examine whether the protection conferred by CpG-ODNs in a schistosome egg-egg antigen murine model of asthma is dependent on the induction of IFN-gamma, IL-12, or both.
C57BL/6 mice were sensitized to schistosome eggs in the presence or absence of CpG-ODNs or control ODNs and then stimulated with soluble egg antigen in the airway. The protection offered by CpG-ODNs in these mice was compared with the protection induced by CpG-ODNs in IL-12 and IFN-gamma knockout mice and in mice treated with anticytokine blocking antibodies. Double-knockout mice (IL-12/IFN-gamma) were also generated and used in these studies. Determinations included airway eosinophilic inflammation and bronchial hyperreactivity to inhaled methacholine.
We found that CpG-ODNs confer protection against both airway eosinophilia and bronchial hyperreactivity in the absence of IFN-gamma or IL-12 or in the presence of both cytokines together. However, in the absence of either IL-12 or IFN-gamma, mice require 10 times as much CpG-ODNs to be protected against the induction of airway eosinophilia. The T(H2) cytokines IL-4 and IL-5 were reduced in all of the CpG-treated mice, although less in the absence of IL-12 and IFN-gamma.
These data indicate that CpG-ODNs prevent the generation of T(H2)-like immune responses by multiple mechanisms, which involve, but do not require, IL-12 and IFN-gamma. A direct suppressive effect of CpG-ODNs on T(H2) responses is suggested by their reduction in IFN-gamma and IL-12 knockout mice.
含有特定序列上下文的二核苷酸CpG的寡脱氧核苷酸(ODN)(CpG-ODN)能够在哮喘小鼠模型中预防嗜酸性气道炎症和支气管高反应性的发展。我们之前已经证明,CpG-ODN在哮喘小鼠模型中刺激诱导T(H1)的细胞因子IFN-γ和IL-12的表达,并且这种刺激与对哮喘炎症的保护作用相关。
本研究的目的是检查在血吸虫卵-卵抗原小鼠哮喘模型中,CpG-ODN赋予的保护作用是否依赖于IFN-γ、IL-12或两者的诱导。
将C57BL/6小鼠在有或无CpG-ODN或对照ODN的情况下对血吸虫卵致敏,然后在气道中用可溶性卵抗原刺激。将这些小鼠中CpG-ODN提供的保护作用与IL-12和IFN-γ基因敲除小鼠以及用抗细胞因子阻断抗体处理的小鼠中CpG-ODN诱导的保护作用进行比较。还制备了双敲除小鼠(IL-12/IFN-γ)并用于这些研究。测定包括气道嗜酸性炎症和对吸入乙酰甲胆碱的支气管高反应性。
我们发现,在没有IFN-γ或IL-12或两者同时存在的情况下,CpG-ODN对气道嗜酸性粒细胞增多和支气管高反应性均有保护作用。然而,在没有IL-12或IFN-γ的情况下,小鼠需要10倍剂量的CpG-ODN才能免受气道嗜酸性粒细胞增多的诱导。在所有经CpG处理的小鼠中,T(H2)细胞因子IL-4和IL-5均减少,尽管在没有IL-12和IFN-γ的情况下减少程度较小。
这些数据表明,CpG-ODN通过多种机制预防类似T(H2)的免疫反应的产生,这些机制涉及但不需要IL-12和IFN-γ。CpG-ODN在IFN-γ和IL-12基因敲除小鼠中的减少提示其对T(H2)反应有直接抑制作用。