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Interferon activation and innate immunity

机译:干扰素激活和先天免疫

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The interferons are a family of cytokine mediators critically involved in alerting the cellular immune system to viral infection of host cells. Interferons not only exhibit important antiviral effects but also exert a key influence on the quality of the cellular immune responses and amplify antigen presentation to specific T cells. Type I interferon (IFN-α and IFN-β) is secreted by virus-infected cells while type II, immune or gamma interferon (IFN-γ) is mainly secreted by T cells, natural killer (NK) cells and macrophages. Interferons interact with specific cellular receptors, which promote production of second messengers ultimately leading to expression of antiviral and immune modulatory genes. The IFN genes themselves are regulated by transcriptional and posttranscriptional mechanisms including modulation by a family of interferon regulatory factors (IRFs) synthesised by host cells. IFNs activate macrophages, induce B cells to switch immunoglobulin type, alter T helper response, inhibit cell growth, promote apoptosis and induce an antiviral state in uninfected cells. The therapeutic potential of the IFNs is currently the focus of intense attention in a number of virusassociated diseases, tumours and autoimmune disorders.
机译:干扰素是一系列细胞因子介体,主要参与提醒细胞免疫系统注意宿主细胞的病毒感染。干扰素不仅显示出重要的抗病毒作用,而且对细胞免疫反应的质量产生关键影响,并放大了向特定T细胞的抗原呈递。 I型干扰素(IFN-α和IFN-β)由病毒感染的细胞分泌,而II型免疫或γ干扰素(IFN-γ)主要由T细胞,自然杀伤(NK)细胞和巨噬细胞分泌。干扰素与特定的细胞受体相互作用,从而促进第二信使的产生,最终导致抗病毒和免疫调节基因的表达。 IFN基因本身受转录和转录后机制的调控,包括受宿主细胞合成的干扰素调节因子(IRF)家族的调节。 IFN激活巨噬细胞,诱导B细胞转换免疫球蛋白类型,改变T辅助反应,抑制细胞生长,促进细胞凋亡,并在未感染的细胞中诱导抗病毒状态。目前,在许多与病毒有关的疾病,肿瘤和自身免疫性疾病中,IFNs的治疗潜力成为人们关注的焦点。

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