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Tumor necrosis factor alpha in cerebrospinal fluid during bacterial but not viral meningitis. Evaluation in murine model infections and in patients

机译:细菌性脑膜炎(而非病毒性脑膜炎)期间脑脊液中的肿瘤坏死因子α。鼠模型感染和患者评估

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摘要

To evaluate the potential role of cachectin/TNF-alpha in the pathogenesis of bacterial and viral meningitis, concentrations and kinetics of TNF-alpha were determined in cerebrospinal fluid (CSF). After intracerebral, but not systemic, infection with Listeria monocytogenes in mice, TNF-alpha was detected as early as 3 h after infection reaching maximum titers after 24 h. However, TNF-alpha was not found in serum during the course of Listeria infection. In contrast to bacterial meningitis, no TNF-alpha was detected at any time in CSF of mice suffering from severe lymphocytic choriomeningitis induced by intracerebral infection with lymphocytic choriomeningitis virus. This difference is striking since both model infections led to a massive infiltration of polymorphonuclear and mononuclear leukocytes into the meninges and CSF. The results found for the two model infections were paralleled by findings in humans; CSF from three out of three patients with bacterial meningitis examined during the first day of hospitalization showed significant levels of TNF-alpha; none of the CSF obtained later than 3 d after hospitalization was positive. In addition, similarly to what was found in mice with viral meningitis, zero out of seven patients with viral meningitis had detectable TNF- alpha in CSF.
机译:为了评估Cachectin /TNF-α在细菌性和病毒性脑膜炎发病机理中的潜在作用,测定了脑脊液(CSF)中TNF-α的浓度和动力学。在小鼠脑内但非全身性感染单核细胞增生性李斯特菌后,最早在感染后3小时就检测到TNF-α,在24小时后达到最大滴度。但是,在李斯特菌感染过程中血清中未发现TNF-α。与细菌性脑膜炎相反,在任何时候由于脑内感染淋巴细胞性脉络膜脑膜炎病毒引起的严重淋巴细胞性脉络膜脑膜炎的小鼠的CSF中均未检测到TNF-α。这种差异是惊人的,因为两种模型感染都导致多形核和单核白细胞大量渗入脑膜和CSF。这两种模型感染的发现结果与人类发现相平行。住院第一天检查的细菌性脑膜炎患者中,三分之三的脑脊液显示出显着水平的TNF-α。住院后3 d获得的脑脊液均无阳性。此外,类似于在病毒性脑膜炎小鼠中发现的情况,七名病毒性脑膜炎患者中有零个在脑脊液中可检测到TNF-α。

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