Institut de Recherche en Immunologie et en Cancérologie (IRIC), Montréal, Québec, Canada.
Curr Opin Virol. 2012 Oct;2(5):622-8. doi: 10.1016/j.coviro.2012.08.009. Epub 2012 Sep 25.
Interferons (IFNs) have long been used as an immunomodulatory therapy for a large array of acute and chronic viral infections. However, IFN therapies have been plagued by severe side effects. The discovery of pathogen recognition receptors (PRR) rejuvenated the interest for immunomodulatory therapies. The successes obtained with Toll-like receptor (TLR) agonists in activating immune cells and as adjuvant for prophylactic vaccines against different viruses paved the way to targeted immunomodulatory therapy. Better characterization of pathogen-induced immune disorders and newly discovered regulators of innate immunity have now the potential to specifically withdraw prevailing subversion mechanisms and to transform antiviral treatments by introducing panviral therapeutics with less adverse effects than IFN therapies.
干扰素 (IFN) 长期以来一直被用作治疗多种急性和慢性病毒感染的免疫调节疗法。然而,IFN 治疗一直受到严重副作用的困扰。病原体识别受体 (PRR) 的发现重新激发了人们对免疫调节治疗的兴趣。Toll 样受体 (TLR) 激动剂在激活免疫细胞和作为针对不同病毒的预防性疫苗佐剂方面取得的成功,为靶向免疫调节治疗铺平了道路。对病原体引起的免疫紊乱的更好描述以及新发现的先天免疫调节剂现在有可能专门消除占主导地位的颠覆机制,并通过引入比 IFN 治疗副作用更少的泛病毒治疗方法来改变抗病毒治疗。