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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性脑膜炎的疗效:一项随机对照试验

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Background We compared adjunctive treatment with placebo, dexamethasone, anti-C5 antibodies, and the combination of dexamethasone plus anti-C5 antibodies in experimental pneumococcal meningitis. Methods 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. Results 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. Conclusion 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:背景我们比较了安慰剂,地塞米松,抗C5抗体和地塞米松加抗C5抗体在实验性肺炎球菌性脑膜炎中的辅助治疗。方法在一项前瞻性,研究者双盲的随机试验中,对96只小鼠的脑池内进行了10 7 CFU / ml肺炎链球菌血清型3感染,在腹腔内注射头孢曲松20小时,并随机分配给安慰剂(盐水),地塞米松腹膜内辅助治疗,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。结果死亡率为安慰剂组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只中的18只地塞米松加抗C5抗体组中的小鼠(60%)(Fisher's精确检验总体差异,P ==。012)。地塞米松加抗C5抗体治疗的小鼠的死亡率低于抗C5抗体治疗的小鼠(log-rank P?= ?. 039)和地塞米松治疗的小鼠(log-rank P?= ?. 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)和地塞米松处理的小鼠(0.249点/小时,P 1 = 0.01.012)。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。结论地塞米松加抗C5抗体的辅助治疗可提高由3型肺炎链球菌血清型引起的严重实验性脑膜炎的存活率,为肺炎球菌脑膜炎的治疗提供了重要的新策略。

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