Cesar Aguilar Julio, Y Lobaina
Department of Hepatitis B, Biomedical Research Unit, Center for Genetic Engineering and Biotechnology, Havana, Cuba.
Euroasian J Hepatogastroenterol. 2014 Jul-Dec;4(2):92-97. doi: 10.5005/jp-journals-10018-1109. Epub 2014 Jul 28.
Despite the existence of effective prophylactic vaccines, hepatitis B virus (HBV) infections remain a major public health problem. It has been estimated that about 370 million people are chronically infected with this virus worldwide. These individuals act as a reservoir for viral spread and chronic infection also increases the risk of liver diseases, such as cirrhosis and hepatocellular carcinoma. Current antiviral therapies fail to control viral replication in the long term in most patients. Viral persistence has been associated with a defect in the development of HBV-specific cellular immunity. The limitations of the current available therapies underline the need for alternative therapies. Specific immunotherapeutic strategies target not only the induction or stimulation of CD4(+) and CD8(+) T-cell responses but also the induction of proinflammatory cytokines capable of controlling viral replication. Therapeutic vaccination has been extensively studied in chronic hepatitis B (CHB) based in the properties of hepatitis B surface antigen (HBsAg) and taking advantage of its previous use in preventive vaccination. In this sense, pioneer studies were carried out employing HBsAg-based vaccines, including prophylactic commercial vaccines and HBsAg-based formulations with novel adjuvants. The results and general knowledge coming from these studies are discussed in the present review. The decision on developing new generations of vaccines including new antigens or formulations should take into account the experience with HBsAg-based vaccine formulations in order to decide about changing the vaccine antigen or adding new antigens to improve the composition. Aguilar JC, Lobaina Y. Immunotherapy for Chronic Hepatitis B using HBsAg-based Vaccine Formulations: From Preventive Commercial Vaccines to Therapeutic Approach. Euroasian J Hepato-Gastroenterol 2014;4(2):92-97.
尽管存在有效的预防性疫苗,但乙型肝炎病毒(HBV)感染仍然是一个重大的公共卫生问题。据估计,全球约有3.7亿人慢性感染这种病毒。这些个体是病毒传播的储存库,慢性感染还会增加患肝硬化和肝细胞癌等肝脏疾病的风险。目前的抗病毒疗法在大多数患者中无法长期控制病毒复制。病毒持续存在与HBV特异性细胞免疫发育缺陷有关。现有疗法的局限性凸显了替代疗法的必要性。特定的免疫治疗策略不仅针对诱导或刺激CD4(+)和CD8(+) T细胞反应,还针对诱导能够控制病毒复制的促炎细胞因子。基于乙型肝炎表面抗原(HBsAg)的特性并利用其在预防性疫苗接种中的先前应用,治疗性疫苗已在慢性乙型肝炎(CHB)中得到广泛研究。从这个意义上说,开展了一些开创性研究,采用基于HBsAg的疫苗,包括预防性商业疫苗和含有新型佐剂的基于HBsAg的制剂。本综述讨论了这些研究的结果和一般知识。在决定开发包括新抗原或制剂的新一代疫苗时,应考虑基于HBsAg的疫苗制剂的经验,以便决定是否改变疫苗抗原或添加新抗原以改善其组成。 阿吉拉尔JC,洛巴伊纳Y。使用基于HBsAg的疫苗制剂治疗慢性乙型肝炎:从预防性商业疫苗到治疗方法。《欧亚肝脏胃肠病学杂志》2014年;4(2):92 - 97。