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高滴度脂多糖抗体血清用于脓毒症和脓毒性休克患者的初步研究

Preliminary study on administration of high-titer lipid A antibody serum in sepsis and septic shock patients.

作者信息

Marget W, Mar P J, Jaspers L, Possinger K, Haslberger H

出版信息

Infection. 1985 May-Jun;13(3):120-4. doi: 10.1007/BF01642870.

Abstract

To determine whether sera containing high titers of lipid A antibody may be applicable at effective doses in treating patients with septicemia, a pharmacokinetic study was performed in seven patients aged 24 to 73 years with gram-negative septicemia and various underlying diseases, one of whom received a placebo, and in one patient without infection. In this study, we attempted to determine the effective dosage, the number of infusions and appropriate administration interval for the prevention and treatment of endotoxin shock. Blood samples from each patient were tested for lipid A antibodies before and at regular intervals after administration using an enzyme-linked immunosorbent assay (ELISA). Selected, pooled human immunoglobulin preparations containing high titers (expressed as exponents of 10) of IgG (titer = 3-4) and IgM (titer = 2-4) lipid A antibodies were administered first at a dosage of 8 ml/kg body weight. After administration, the mean lipid A antibody titer increased from 0.4 to 2.3 for IgG and from 2 to 2.4 for IgM. The initial increase was followed by a drop in titer within 24 h, which was perhaps due to antibody consumption. Following the second administration (24 h after the first) of only 4 ml/kg body weight, the mean IgG and IgM titers increased to 2.4 and 3.3, respectively, and dropped slower. A notable increase in circulating lipid A antibody titers was achieved, and four of six treated patients recovered from the sepsis. The two patients who died entered the study in a pre-terminal state. These studies encouraged us to initiate a randomized, double-blind controlled study.

摘要

为了确定含有高滴度脂多糖抗体的血清是否能以有效剂量用于治疗败血症患者,我们对7名年龄在24至73岁之间、患有革兰氏阴性败血症及各种基础疾病的患者进行了一项药代动力学研究,其中1名患者接受了安慰剂,还有1名未感染的患者也参与了研究。在这项研究中,我们试图确定预防和治疗内毒素休克的有效剂量、输注次数及合适的给药间隔。在给药前及给药后的定期时间点,采集每位患者的血样,使用酶联免疫吸附测定法(ELISA)检测脂多糖抗体。首先以8毫升/千克体重的剂量给予选定的、汇集的含有高滴度(以10的指数表示)IgG(滴度 = 3 - 4)和IgM(滴度 = 2 - 4)脂多糖抗体的人免疫球蛋白制剂。给药后,IgG的平均脂多糖抗体滴度从0.4升至2.3,IgM从2升至2.4。最初滴度升高后,24小时内滴度下降,这可能是由于抗体消耗所致。在首次给药24小时后第二次仅以4毫升/千克体重给药后,IgG和IgM的平均滴度分别升至2.4和3.3,且下降速度更慢。循环脂多糖抗体滴度显著升高,6名接受治疗的患者中有4名败血症痊愈。死亡的2名患者在进入研究时已处于濒死状态。这些研究促使我们开展一项随机、双盲对照研究。

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