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Adjuvant treatment with dexamethasone plus anti-C5 antibodies improves outcome of experimental pneumococcal meningitis: a randomized controlled trial

机译:地塞米松加抗C5抗体的辅助治疗可改善实验性肺炎球菌脑膜炎的疗效:一项随机对照试验

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摘要

We compared adjunctive treatment with placebo, dexamethasone, anti-C5 antibodies, and the combination of dexamethasone plus anti-C5 antibodies in experimental pneumococcal meningitis. In this prospective, investigator-blinded, randomized trial, 96 mice were infected intracisternally with 10(7) CFU/ml Streptococcus pneumoniae serotype 3, treated with intraperitoneal ceftriaxone at 20 h, and randomly assigned to intraperitoneal adjunctive treatment with placebo (saline), dexamethasone, anti-C5 antibodies, or dexamethasone plus anti-C5 antibodies. The primary outcome was survival during a 72-h observational period that was analyzed with the log-rank test. Secondary outcome was clinical severity, scored on a validated scale using a linear mixed model. Mortality rates were 16 of 16 mice (100%) in the placebo group, 12 of 15 mice (80%) in the dexamethasone group, 25 of 31 mice (80%) in the anti-C5 antibody group, and 18 of 30 mice (60%) in the dexamethasone plus anti-C5 antibody group (Fisher's exact test for overall difference, P = .012). Mortality of mice treated with dexamethasone plus anti-C5 antibodies was lower compared to the anti-C5 antibody-treated mice (log-rank P = .039) and dexamethasone-treated mice (log-rank P = .040). Clinical severity scores for the dexamethasone plus anti-C5 antibody-treated mice increased more slowly (0.199 points/h) as compared to the anti-C5 antibody-treated mice (0.243 points/h, P = .009) and dexamethasone-treated mice (0.249 points/h, P = .012). Modeling of severity data suggested an additive effect of dexamethasone and anti-C5 antibodies. Adjunctive treatment with dexamethasone plus anti-C5 antibodies improves survival in severe experimental meningitis caused by S. pneumoniae serotype 3, posing an important new treatment strategy for patients with pneumococcal meningitis
机译:我们在实验性肺炎球菌性脑膜炎中比较了安慰剂,地塞米松,抗C5抗体和地塞米松加抗C5抗体的辅助治疗。在这项前瞻性,研究者盲目的随机试验中,96例小鼠被10例(7)CFU / ml肺炎链球菌血清型3进行了脑池内感染,在20 h时用腹膜内头孢曲松进行了治疗,并随机分配了安慰剂(盐水)进行腹膜内辅助治疗,地塞米松,抗C5抗体或地塞米松加抗C5抗体。主要结果是在72小时观察期内的生存率,并通过对数秩检验进行了分析。次要结果是临床严重性,使用线性混合模型在有效范围内评分。死亡率为安慰剂组16只小鼠中的16只(100%),地塞米松组15只小鼠中的12只(80%),抗C5抗体组31只小鼠中的25只(80%)和30只小鼠中的18只(60%)在地塞米松加抗C5抗体组中(Fisher的整体差异精确检验,P = .012)。用地塞米松加抗C5抗体治疗的小鼠的死亡率低于用抗C5抗体治疗的小鼠(对数秩P = 0.039)和地塞米松治疗的小鼠(对数秩P = 0.040)。地塞米松加抗C5抗体治疗的小鼠的临床严重程度评分与抗C5抗体治疗的小鼠(0.243点/ h,P = 0.009)和地塞米松治疗的小鼠相比,增幅更为缓慢(0.199点/ h)。 (0.249点/小时,P = .012)。对严重性数据进行建模表明,地塞米松和抗C5抗体具有累加作用。地塞米松加抗C5抗体的辅助治疗可改善由肺炎链球菌血清型3引起的严重实验性脑膜炎的存活率,为肺炎球菌脑膜炎患者提出了重要的新治疗策略

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