Gehring Adam J
Toronto Centre for Liver Disease and Toronto General Hospital Research Institute, University Health Network, Toronto, Canada; Department of Immunology, University of Toronto, Toronto, Canada.
Best Pract Res Clin Gastroenterol. 2017 Jun;31(3):337-345. doi: 10.1016/j.bpg.2017.05.004. Epub 2017 May 25.
The landscape for chronic HBV therapy is rapidly evolving. The latest generation of antiviral drugs provide robust virus suppression with a high barrier to resistance that facilitates long-term treatment. However, low rates of HBsAg loss demonstrate that additional strategies are needed to consistency achieve a functional cure. The immune system can clear HBV and establish long-term control over the virus. Sufficiently boosting HBV immunity in chronic patients has been very difficult due to immune exhaustion, immune dysregulation, and inhibitory pathways suppressing the immune response. Therapeutic vaccines employing new technology, vectors and new immunomodulatory drugs that can elicit direct antiviral effects and cancel inhibitory mechanism may be able to overcome exhaustion. This review will discuss the justification for immunotherapy, lessons from previous trials and new vaccines/drugs in early stage clinical trials. The challenges of correlating immune responses induced by these drugs to clinical efficacy will also be addressed.
慢性乙肝治疗的格局正在迅速演变。最新一代抗病毒药物能有效抑制病毒,且具有高耐药屏障,便于长期治疗。然而,乙肝表面抗原(HBsAg)转阴率较低,这表明需要额外的策略来持续实现功能性治愈。免疫系统可以清除乙肝病毒并建立对病毒的长期控制。由于免疫耗竭、免疫失调以及抑制免疫反应的抑制途径,在慢性患者中充分增强乙肝免疫力一直非常困难。采用新技术、载体和新型免疫调节药物的治疗性疫苗,能够引发直接抗病毒作用并消除抑制机制,或许能够克服免疫耗竭。本综述将讨论免疫治疗的依据、既往试验的经验教训以及早期临床试验中的新疫苗/药物。还将探讨将这些药物诱导的免疫反应与临床疗效相关联所面临的挑战。