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病毒感染中的IRF3:不仅仅是触发干扰素反应。

IRF3 in viral infections: more than just triggering the interferon response.

作者信息

Bourdon Marie, Manet Caroline, Montagutelli Xavier

机构信息

Institut Pasteur, Université Paris Cité, Mouse Genetics Laboratory, Paris, France.

Institut Pasteur, Université Paris Cité, Mouse Genetics, Immunity and Infections Laboratory, Paris, France.

出版信息

Genes Immun. 2025 Sep 2. doi: 10.1038/s41435-025-00354-2.

Abstract

Interferon regulatory factor 3 (IRF3) is the first transcription factor activating the expression of type I interferons (IFN-I). It is present in the cytoplasm of most cell types under basal conditions and its activation by phosphorylation allows a rapid triggering of the IFN-I pathway in response to viral infection. This activation of IFN-I is amplified by IRF7, the other major IFN-I transcription factor which expression is induced, in most cell types, by the interferon response. However, recent data have shown that the role of IRF3 in viral infection extends beyond the IFN-I pathway. Here, we review the studies investigating the impact of IRF3 deficiencies in infected cells and in vivo, in mice and in humans. We discuss the discrepancies between and within studies, between isolated cells and whole organisms. While IRF3 is also involved in other pathological processes, we highlight how the newly discovered functions of IRF3 deepen our understanding of its multiple roles in viral infections, which could stimulate the development of pharmacological manipulation of its biological activities.

摘要

干扰素调节因子3(IRF3)是第一个激活I型干扰素(IFN-I)表达的转录因子。在基础条件下,它存在于大多数细胞类型的细胞质中,其通过磷酸化激活能够在病毒感染时快速触发IFN-I途径。IFN-I的这种激活由IRF7放大,IRF7是另一个主要的IFN-I转录因子,在大多数细胞类型中,其表达由干扰素反应诱导。然而,最近的数据表明,IRF3在病毒感染中的作用超出了IFN-I途径。在这里,我们综述了研究IRF3缺陷对感染细胞以及在小鼠和人类体内影响的研究。我们讨论了不同研究之间以及同一研究中分离细胞和整个生物体之间的差异。虽然IRF3也参与其他病理过程,但我们强调IRF3新发现的功能如何加深我们对其在病毒感染中多种作用的理解,这可能会促进对其生物学活性进行药理学操纵的研究进展。

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