RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Antiviral therapy for hepatitis B virus infection is beneficial for the prognosis hepatocellular carcinoma.
Antiviral therapy for hepatitis B virus infection is beneficial for the prognosis hepatocellular carcinoma.
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在这篇社论中,我们对Mu等发表于近期《世界胃肠肿瘤学杂志》的文章进行评论。我们特别关注乙型肝炎病毒(HBV)感染所致的免疫耐受机制、肝细胞癌(HCC)的发病机制,以及抗病毒治疗在治疗HBV感染相关HCC中的作用。HBV感染通过直接抑制模式识别受体识别和抗病毒信号通路,以及抑制巨噬细胞、NK 细胞和树突状细胞的免疫功能,导致全身性先天免疫耐受。此外,HBV通过表达抑制性分子诱导HBV特异性分化簇8+ T细胞耗竭,从而引发免疫抑制级联反应,最终导致长期病毒感染。HBV感染引起的免疫细胞功能丧失最终导致HCC。长期抗病毒治疗可改善HCC患者的预后,并预防肿瘤复发和转移。
In this editorial, we comment on the article by Mu et al , published in the recent issue of the World Journal of Gastrointestinal Oncology .
We pay special attention to the immune tolerance mechanism caused by hepatitis B virus (HBV) infection, the pathogenesis of hepatocellular carcinoma (HCC), and the role of antiviral therapy in treating HCC related to HBV infection. HBV infection leads to systemic innate immune tolerance by directly inhibiting pattern recognition receptor recognition and antiviral signaling pathways, as well as by inhibiting the immune functions of macrophages, natural killer cells and dendritic cells.
In addition, HBV leads to an immunosuppressive cascade by expressing inhibitory molecules to induce exhaustion of HBV-specific cluster of differentiation 8 + T cells, ultimately leading to long-term viral infection. The loss of immune cell function caused by HBV infection ultimately leads to HCC. Long-term antiviral therapy can improve the prognosis of patients with HCC and prevent tumor recurrence and metastasis.
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