调节性T细胞在乙型和丙型肝炎中的免疫生物学研究

T. Susilawati, A. Permata, S. Setyawan
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引用次数: 0

摘要

乙型和丙型肝炎仍然是世界上具有挑战性的问题。目前可用的抗病毒药物和干扰素治疗的结果并不令人满意,新获得性感染的数量继续增加。这种情况促使人们研究新的方法来降低乙型和丙型肝炎患者的死亡率和发病率。在以前的研究中已经报道了调节性T细胞(Tregs)在疾病各个阶段的动态。尽管Tregs介导的肝炎免疫的全面机制尚不清楚,但已有研究认为Tregs可能在维持病毒持续和预防肝损伤方面发挥重要作用。为了了解调节性T细胞在乙型和丙型肝炎中的免疫生物学作用,我们回顾了在线数据库中可获得的原始研究文章。我们发现,在乙型肝炎中,Tregs的发育受浆细胞样树突状细胞、可溶性热休克蛋白(HSP)-60和toll样受体(TLR) 2/4信号的影响。肿瘤生长因子(TGF)-β、吲哚胺2,3-双加氧酶(IDO)、Tim-3/Gal-9相互作用、toll样受体(TLR)-2刺激、Notch信号、hcv诱导的miR146a、Tregs在HBV感染的肝脏中抑制细胞毒性T细胞的功能,而肝内Tregs产生的白细胞介素(IL)-8有助于Tregs在慢性丙型肝炎中发挥调节纤维化的作用。本文报道了Tregs在乙型肝炎和丙型肝炎中的意义,以及它们在HBV和HCV感染背景下的发展和抑制。乙型和丙型肝炎仍然是世界上具有挑战性的问题。目前可用的抗病毒药物和干扰素治疗的结果并不令人满意,新获得性感染的数量继续增加。这种情况促使人们研究新的方法来降低乙型和丙型肝炎患者的死亡率和发病率。在以前的研究中已经报道了调节性T细胞(Tregs)在疾病各个阶段的动态。尽管Tregs介导的肝炎免疫的全面机制尚不清楚,但已有研究认为Tregs可能在维持病毒持续和预防肝损伤方面发挥重要作用。为了了解调节性T细胞在乙型和丙型肝炎中的免疫生物学作用,我们回顾了在线数据库中可获得的原始研究文章。我们发现,在乙型肝炎中,Tregs的发育受浆细胞样树突状细胞、可溶性热休克等因素的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The immunobiology of regulatory T cells in hepatitis B and C
Hepatitis B and C continue to be the world challenging problems. The results of currently available treatments with antiviral medications and interferon-based therapy have not been satisfactory and the numbers of newly acquired infection continue to increase. This situation has prompted investigations into novel approaches to decrease the mortality and morbidity of those suffering from hepatitis B and C. The dynamics of regulatory T cells (Tregs) in various stages of the illness have been reported in previous studies. It has been asserted that Tregs may have important roles in sustaining the viral persistence and preventing liver damage although the comprehensive mechanisms of hepatitis immunity mediated by Tregs are not well understood. To understand the immunobiology of regulatory T cells in hepatitis B and hepatitis C, we reviewed original research articles available from online databases. We found that in hepatitis B, Tregs development is influenced by plasmacytoid dendritic cells, soluble heat shock protein (HSP)-60, and toll-like receptor (TLR) 2/4 signaling. Tumor growth factor (TGF)-β, indoleamine 2,3-dioxygenase (IDO), Tim-3/Gal-9 interactions, toll-like receptor (TLR)-2 stimulation, Notch signaling, HCV-induced miR146a, and contact with dendritic cells or B cells promote Tregs development and activation in hepatitis C. Tregs inhibit the function of cytotoxic T cells in HBV-infected livers whereas interleukin (IL)-8 produced by intrahepatic Tregs contributes to Tregs’ role as the regulator of fibrogenesis in chronic hepatitis C. This present paper reports the significance of Tregs in hepatitis B and C as well as their development and suppression in the context of HBV and HCV infection.Hepatitis B and C continue to be the world challenging problems. The results of currently available treatments with antiviral medications and interferon-based therapy have not been satisfactory and the numbers of newly acquired infection continue to increase. This situation has prompted investigations into novel approaches to decrease the mortality and morbidity of those suffering from hepatitis B and C. The dynamics of regulatory T cells (Tregs) in various stages of the illness have been reported in previous studies. It has been asserted that Tregs may have important roles in sustaining the viral persistence and preventing liver damage although the comprehensive mechanisms of hepatitis immunity mediated by Tregs are not well understood. To understand the immunobiology of regulatory T cells in hepatitis B and hepatitis C, we reviewed original research articles available from online databases. We found that in hepatitis B, Tregs development is influenced by plasmacytoid dendritic cells, soluble heat shock ...
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