Hurley J C
Department of Clinical Pathology, Fairfield Hospital, Victoria, Australia.
Clin Infect Dis. 1992 Nov;15(5):840-54. doi: 10.1093/clind/15.5.840.
A three- to 20-fold increase in the total concentration of endotoxin occurs as a consequence of antibiotic action on gram-negative bacteria both in vitro and in vivo. There is considerable overlap between the effect of beta-lactam antibiotics and non-beta-lactam antibiotics. Moreover, there is an unexplained delay between the lethal activity of antibiotics and the release of endotoxin. Hence, the mechanism whereby antibiotic action leads to the release of endotoxin is unclear, and mechanisms other than bacterial lysis warrant consideration. The evidence that the release of endotoxin has clinical importance is conflicting, and the issue is unresolved. However, nonlytic release may have implications for the therapeutic efficacy of antiendotoxin immunotherapy. Although frequently cited in the context of the antibiotic-induced release of endotoxin, a number of important differences pertain to conditions, such as the Jarisch-Herxheimer reaction and the tumor lysis syndrome, for which there is clear evidence of an initial deterioration with effective therapy.
在体外和体内,抗生素作用于革兰氏阴性菌会导致内毒素总浓度增加3至20倍。β-内酰胺类抗生素和非β-内酰胺类抗生素的作用有相当大的重叠。此外,抗生素的致死活性与内毒素释放之间存在无法解释的延迟。因此,抗生素作用导致内毒素释放的机制尚不清楚,除细菌裂解外的其他机制值得考虑。关于内毒素释放具有临床重要性的证据相互矛盾,这个问题尚未解决。然而,非裂解性释放可能对抗内毒素免疫治疗的疗效有影响。尽管在抗生素诱导的内毒素释放背景下经常被提及,但一些重要差异与诸如雅里希-赫克斯海默反应和肿瘤溶解综合征等情况有关,对于这些情况,有明确证据表明有效治疗后最初会出现病情恶化。