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实验性细菌性脑膜炎期间脑脊液(CSF)中细胞因子和抗细胞因子自身抗体的诱导。

Induction of cytokines and anti-cytokine autoantibodies in cerebrospinal fluid (CSF) during experimental bacterial meningitis.

作者信息

Bakhiet M, Mustafa M, Zhu J, Harris R, Lindquist L, Link H, Diab A

机构信息

Divisions of Neurology and Infectious Diseases, Karolinska Institute, Huddinge University Hospital, Huddinge, Sweden.

出版信息

Clin Exp Immunol. 1998 Dec;114(3):398-402. doi: 10.1046/j.1365-2249.1998.00742.x.

DOI:10.1046/j.1365-2249.1998.00742.x
PMID:9844049
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1905126/
Abstract

We have recently described the induction of anti-cytokine autoantibodies (Aabs) in the serum as a novel mechanism for cytokine regulation during bacterial infections. Here we use the infant rat-model of Haemophilus influenzae type b (Hib) meningitis to examine the induction of five potentially important cytokines and their autoantibody responses in the CSF. Protein levels of the cytokines interferon-gamma (IFN-gamma), tumour necrosis factor-alpha (TNF-alpha), transforming growth factor-beta (TGF-beta), IL-4 and IL-10 were detected at day 3 post-inoculation (p.i.) with maximum induction at day 8. Thereafter, these levels of cytokines had become undetectable. Increased Aab titres to these cytokines, except IL-4, were registered with peak levels between days 7 and 9. Upon re-inoculation with Hib at day 30, regeneration of Aabs was recorded 7 days later (i.e. at day 37). To control the specificity of these Aabs, preincubation of the CSF with a cytokine inhibited the binding effects of that particular cytokine, but not those of any other cytokine. Aabs dose-dependently inhibited IFN-gamma-induced MHC expression by peritoneal macrophages and TNF-alpha-mediated L929 cytotoxicity. Our data demonstrate for the first time the existence of the anti-cytokine antibodies in the CSF of the meningitis Hib model. Furthermore, the data present a role for the Aabs in cytokine regulation, which is consistent with the previously demonstrated effects of the Aabs in the serum.

摘要

我们最近报道,血清中抗细胞因子自身抗体(Aabs)的诱导是细菌感染期间细胞因子调节的一种新机制。在此,我们使用b型流感嗜血杆菌(Hib)脑膜炎幼鼠模型来检测脑脊液中5种潜在重要细胞因子的诱导情况及其自身抗体反应。接种后第3天(p.i.)检测到细胞因子干扰素-γ(IFN-γ)、肿瘤坏死因子-α(TNF-α)、转化生长因子-β(TGF-β)、白细胞介素-4(IL-4)和白细胞介素-10的蛋白水平,第8天诱导达到最大值。此后,这些细胞因子水平变得无法检测到。除IL-4外,这些细胞因子的Aab滴度增加,在第7天至第9天达到峰值水平。在第30天再次接种Hib后,7天后(即第37天)记录到Aabs的再生。为了控制这些Aabs的特异性,脑脊液与一种细胞因子预孵育可抑制该特定细胞因子的结合效应,但不影响任何其他细胞因子的结合效应。Aabs剂量依赖性地抑制IFN-γ诱导的腹膜巨噬细胞MHC表达以及TNF-α介导的L929细胞毒性。我们的数据首次证明了脑膜炎Hib模型脑脊液中存在抗细胞因子抗体。此外,数据表明Aabs在细胞因子调节中发挥作用,这与之前在血清中证明的Aabs的作用一致。

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本文引用的文献

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Cytokines and anti-cytokine autoantibodies during experimental african trypanosomiasis in mice with disrupted interferon-gamma and interferon-gamma receptor genes.在干扰素-γ和干扰素-γ受体基因被破坏的小鼠实验性非洲锥虫病期间的细胞因子和抗细胞因子自身抗体
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