Manipulation of Regulatory Cells' Responses to Treatments for Chronic Hepatitis B Virus Infection

被引:7
|
作者
Tavakolpour, Soheil [1 ]
Alavian, Seyed Moayed [1 ]
Sali, Shahnaz [2 ]
机构
[1] Baqyiatallah Univ Med Sci, Baqiyatallah Res Ctr Gastroenterol & Liver Dis, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Infect Dis & Trop Med Res Ctr, Tehran, Iran
关键词
Hepatitis B Viruses; Chronic Hepatitis B; Regulatory T Cells; Treg Cells; T-Lymphocytes; CD8(+) T-CELLS; ANTIVIRAL TREATMENT; IMMUNE-RESPONSES; UP-REGULATION; EXPRESSION; TIM-3; BLOCKADE; PD-1; DYSFUNCTION; INHIBITION;
D O I
10.5812/hepatmon.37927
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: 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. Objectives: In this study, we focused on treating CHB infection via the manipulation of T cells' responses to identify possible approaches to cure CHB. Materials and Methods: 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 Considering extracted data and also our unpublished data regarding the association between regulatory cytokines and CHB, we introduced a novel approach for the induction of seroclearance. Results: 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. Conclusions: 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.
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页数:9
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