Tavakolpour Soheil, Alavian Seyed Moayed, Sali Shahnaz
Baqiyatallah Research Center for Gastroenterology and Liver Diseases, Baqyiatallah University of Medical Sciences, Tehran, IR Iran.
Infectious Diseases and Tropical Medicine Research Center, Shahid Beheshti University of Medical Sciences, Tehran, IR Iran.
Hepat Mon. 2016 May 25;16(6):e37927. doi: 10.5812/hepatmon.37927. eCollection 2016 Jun.
Identification of effective treatments in hepatitis B virus (HBV) infection remains a controversial topic. Although the currently approved drugs for HBV control the disease's progression and also limit associated outcomes, these drugs may not fully eradicate HBV infection. In addition to better managing patients with chronic hepatitis B (CHB) infection, the induction of seroclearance by these drugs has been a commonly discussed topic in recent years.
In this study, we focused on treating CHB infection via the manipulation of T cells' responses to identify possible approaches to cure CHB.
All studies relevant to the role of cellular and humoral responses in HBV infection (especially regulatory cells) were investigated via a systematic search of different databases, including PubMed, Scopus, and Google Scholar. Considering extracted data and also our unpublished data regarding the association between regulatory cytokines and CHB, we introduced a novel approach for the induction of seroclearance.
Considering the increased levels of regulatory cytokines and also regulatory T cells (Tregs) during CHB, it seems that these cells are deeply involved in CHB infection. The inhibition of regulatory T cells may reverse the dysfunction of effector T cells in patients with CHB infection. In order to inhibit Tregs' responses, different types of approaches could be employed to restore the impaired function of effector T cells. The blockade of IL-10, IL-35, CTLA-4, PD-1, and TIM-3 were discussed throughout this study. Regardless of the efficacy of these methods, CHB patients may experience serious liver injuries due to the cytotoxic action of CD8+ T cells. Antiviral therapy and a decrease in HBV DNA to undetectable levels could also significantly reduce the risk of the hepatitis B flare.
The inhibition of Tregs is a novel therapeutic approach to cure chronically HBV infected patients. However, further studies are needed to investigate the safety and efficacy of this approach.
确定乙型肝炎病毒(HBV)感染的有效治疗方法仍是一个有争议的话题。尽管目前批准用于HBV的药物可控制疾病进展并限制相关后果,但这些药物可能无法完全根除HBV感染。除了更好地管理慢性乙型肝炎(CHB)感染患者外,近年来这些药物诱导血清学清除一直是一个经常讨论的话题。
在本研究中,我们专注于通过操纵T细胞反应来治疗CHB感染,以确定治愈CHB的可能方法。
通过系统检索不同数据库,包括PubMed、Scopus和谷歌学术,调查了所有与细胞和体液反应在HBV感染(尤其是调节性细胞)中的作用相关的研究。考虑到提取的数据以及我们关于调节性细胞因子与CHB之间关联的未发表数据,我们引入了一种诱导血清学清除的新方法。
考虑到CHB期间调节性细胞因子和调节性T细胞(Tregs)水平升高,似乎这些细胞深度参与CHB感染。抑制调节性T细胞可能会逆转CHB感染患者效应T细胞的功能障碍。为了抑制Tregs的反应,可以采用不同类型的方法来恢复效应T细胞受损的功能。本研究讨论了对白细胞介素-10(IL-10)、IL-35、细胞毒性T淋巴细胞相关蛋白4(CTLA-4)、程序性死亡受体1(PD-1)和T细胞免疫球蛋白和粘蛋白结构域3(TIM-3)的阻断。无论这些方法的疗效如何,CHB患者可能会因CD8 + T细胞的细胞毒性作用而出现严重肝损伤。抗病毒治疗以及将HBV DNA降低到无法检测的水平也可以显著降低乙型肝炎发作的风险。
抑制Tregs是治疗慢性HBV感染患者的一种新的治疗方法。然而,需要进一步研究来调查这种方法的安全性和有效性。