Dinarello C A
Department of Medicine, Division of Infectious Diseases, University of Colorado Health Sciences Center, Denver 80262, USA.
Chest. 2000 Aug;118(2):503-8. doi: 10.1378/chest.118.2.503.
To review the concept of proinflammatory cytokines.
Review of published literature.
Academic (university hospital).
Cytokines are regulators of host responses to infection, immune responses, inflammation, and trauma. Some cytokines act to make disease worse (proinflammatory), whereas others serve to reduce inflammation and promote healing (anti-inflammatory). Attention also has focused on blocking cytokines, which are harmful to the host, particularly during overwhelming infection. Interleukin (IL)-1 and tumor necrosis factor (TNF) are proinflammatory cytokines, and when they are administered to humans, they produce fever, inflammation, tissue destruction, and, in some cases, shock and death. Reducing the biological activities of IL-1 and TNF is accomplished by several different, but highly specific, strategies, which involve neutralizing antibodies, soluble receptors, receptor antagonist, and inhibitors of proteases that convert inactive precursors to active, mature molecules. Blocking IL-1 or TNF has been highly successful in patients with rheumatoid arthritis, inflammatory bowel disease, or graft-vs-host disease but distinctly has not been successful in humans with sepsis. Agents such as TNF-neutralizing antibodies, soluble TNF receptors, and IL-1 receptor antagonist have been infused into > 10,000 patients in double-blind, placebo-controlled trials. Although there has been a highly consistent small increase (2 to 3%) in 28-day survival rates with anticytokine therapy, the effect has not been statistically significant.
Anticytokine therapy should be able to "rescue" the patient whose condition continues to deteriorate in the face of considerable support efforts. Unfortunately, it remains difficult to identify those patients who would benefit from anticytokine therapy for septic shock.
回顾促炎细胞因子的概念。
对已发表文献的综述。
学术机构(大学医院)。
细胞因子是宿主对感染、免疫反应、炎症和创伤反应的调节因子。一些细胞因子会使疾病恶化(促炎),而另一些则有助于减轻炎症并促进愈合(抗炎)。人们也将注意力集中在阻断对宿主有害的细胞因子上,尤其是在严重感染期间。白细胞介素(IL)-1和肿瘤坏死因子(TNF)是促炎细胞因子,当将它们施用于人体时,会引起发热、炎症、组织破坏,在某些情况下还会导致休克和死亡。通过几种不同但高度特异性的策略可以降低IL-1和TNF的生物活性,这些策略包括中和抗体、可溶性受体、受体拮抗剂以及将无活性前体转化为活性成熟分子的蛋白酶抑制剂。在类风湿性关节炎、炎症性肠病或移植物抗宿主病患者中,阻断IL-1或TNF已取得了很大成功,但在脓毒症患者中显然未取得成功。在双盲、安慰剂对照试验中,已将诸如TNF中和抗体、可溶性TNF受体和IL-1受体拮抗剂等药物输注给了超过10000名患者。尽管使用抗细胞因子疗法使28天生存率有了高度一致的小幅提高(2%至3%),但该效果在统计学上并不显著。
抗细胞因子疗法应该能够“挽救”那些尽管得到了大量支持性治疗但病情仍在持续恶化的患者。不幸的是,仍然难以确定哪些患者会从抗细胞因子疗法治疗感染性休克中获益。