Department of Medicine & Therapeutics, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong.
Department of Medicine & Therapeutics, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong; Division of Infectious Diseases, University of Alberta, Edmonton, Canada.
Antiviral Res. 2018 Feb;150:202-216. doi: 10.1016/j.antiviral.2018.01.002. Epub 2018 Jan 8.
A severe inflammatory immune response with hypercytokinemia occurs in patients hospitalized with severe influenza, such as avian influenza A(H5N1), A(H7N9), and seasonal A(H1N1)pdm09 virus infections. The role of immunomodulatory therapy is unclear as there have been limited published data based on randomized controlled trials (RCTs). Passive immunotherapy such as convalescent plasma and hyperimmune globulin have some studies demonstrating benefit when administered as an adjunctive therapy for severe influenza. Triple combination of oseltamivir, clarithromycin, and naproxen for severe influenza has one study supporting its use, and confirmatory studies would be of great interest. Likewise, confirmatory studies of sirolimus without concomitant corticosteroid therapy should be explored as a research priority. Other agents with potential immunomodulating effects, including non-immune intravenous immunoglobulin, N-acetylcysteine, acute use of statins, macrolides, pamidronate, nitazoxanide, chloroquine, antiC5a antibody, interferons, human mesenchymal stromal cells, mycophenolic acid, peroxisome proliferator-activated receptors agonists, non-steroidal anti-inflammatory agents, mesalazine, herbal medicine, and the role of plasmapheresis and hemoperfusion as rescue therapy have supportive preclinical or observational clinical data, and deserve more investigation preferably by RCTs. Systemic corticosteroids administered in high dose may increase the risk of mortality and morbidity in patients with severe influenza and should not be used, while the clinical utility of low dose systemic corticosteroids requires further investigation.
在因严重流感住院的患者中,会发生严重的炎症免疫反应和细胞因子血症,例如禽流感 A(H5N1)、A(H7N9)和季节性 A(H1N1)pdm09 病毒感染。免疫调节疗法的作用尚不清楚,因为基于随机对照试验 (RCT) 的已发表数据有限。在严重流感的辅助治疗中,使用恢复期血浆和高免疫球蛋白等被动免疫疗法,一些研究表明有获益。对于严重流感,奥司他韦、克拉霉素和萘普生三联疗法有一项研究支持其使用,需要开展确证性研究。同样,应该探索西罗莫司(无伴随皮质类固醇治疗)作为研究重点的优先事项。其他具有潜在免疫调节作用的药物,包括非免疫静脉用免疫球蛋白、N-乙酰半胱氨酸、他汀类药物的急性使用、大环内酯类药物、帕米膦酸、硝唑尼特、氯喹、抗 C5a 抗体、干扰素、人间充质基质细胞、霉酚酸、过氧化物酶体增殖物激活受体激动剂、非甾体抗炎药、美沙拉嗪、草药,以及作为挽救性治疗的血浆置换和血液灌流的作用,具有支持性的临床前或临床观察数据,值得进一步研究,最好通过 RCT 进行。大剂量全身皮质类固醇的使用可能会增加严重流感患者的死亡和发病率风险,因此不应使用,而小剂量全身皮质类固醇的临床应用价值需要进一步研究。