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革兰氏阴性菌血症的抗血清治疗。

Antiserum treatment of gram-negative bacteremia.

作者信息

Braude A I, Ziegler E J, McCutchan J A

出版信息

Schweiz Med Wochenschr. 1978 Dec 2;108(48):1872-6.

PMID:362528
Abstract

In order to lower the mortality rate from gram-negative bacteremia, 136 patients were treated with human antiserum against core glycolipid, or with control nonimmune human serum, in a double-blind clinical trial. The antiserum was prepared by immunizing healthy young men with a vaccine composed of heat killed cells of the J5 mutant of E. coli 0111 B4. Since the core glycolipid in this mutant is not encumbered with "O" side chains, it can stimulate antibody against the core glycolipid possessed in common by the different species of gram-negative bacteria responsible for lethal bacteremia in patients. No serious reactions occurred in over 300 men receiving this vaccine, and the J5 antiserum gave striking broad-spectrum protection against experimental gram-negative bacteremia and endotoxemia. When human J5 antiserum was administered to seriously ill bacteremic patients, the mortality rate was virtually cut in half, as compared to controls. The death rate from gram-negative bacteremia was 14% in patients treated with J5 antiserum, and 26% in those given nonimmune control human serum. Among patients in profound gram-negative bacteremic shock, the recovery rate rose from 29% in controls to 82% in those treated with J5 antiserum (p = 0.02). On the basis of these encouraging results we propose to treat more bacteremic patients with J5 antiserum, because larger groups are needed to establish the full significance of the initial findings.

摘要

为降低革兰氏阴性菌血症的死亡率,在一项双盲临床试验中,136名患者接受了抗核心糖脂人抗血清治疗,或接受对照非免疫人血清治疗。该抗血清是通过用由大肠杆菌0111 B4的J5突变体的热杀死细胞组成的疫苗免疫健康年轻男性制备的。由于该突变体中的核心糖脂没有“O”侧链的阻碍,它可以刺激产生针对导致患者致命菌血症的不同革兰氏阴性菌共同拥有的核心糖脂的抗体。300多名接受这种疫苗的男性没有出现严重反应,J5抗血清对实验性革兰氏阴性菌血症和内毒素血症具有显著的广谱保护作用。当将人J5抗血清给予重症菌血症患者时,与对照组相比,死亡率几乎降低了一半。接受J5抗血清治疗的患者革兰氏阴性菌血症的死亡率为14%,接受非免疫对照人血清治疗的患者为26%。在严重革兰氏阴性菌血症休克患者中,恢复率从对照组的29%上升到接受J5抗血清治疗患者的82%(p = 0.02)。基于这些令人鼓舞的结果,我们建议用J5抗血清治疗更多的菌血症患者,因为需要更大的样本量来确定最初发现的全部意义。

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