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Interferon-ε Protects the Female Reproductive Tract from Viral and Bacterial Infection

机译:干扰素-ε保护女性生殖道免受病毒和细菌感染

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摘要

The innate immune system senses pathogens through pattern-recognition receptors (PRRs) that signal to induce effector cytokines, such as type Ⅰ interferons (IFNs). We characterized IFN-ε as a type Ⅰ IFN because it signaled via the Ifnarl and Ifnar2 receptors to induce IFN-regulated genes. In contrast to other type Ⅰ IFNs, IFN-ε was not induced by known PRR pathways; instead, IFN-ε was constitutively expressed by epithelial cells of the female reproductive tract (FRT) and was hormonally regulated. Ifn-ε-deficient mice had increased susceptibility to infection of the FRT by the common sexually transmitted infections (STIs) herpes simplex virus 2 and Chlamydia muridarum. Thus, IFN-ε is a potent antipathogen and immunoregulatory cytokine that may be important in combating STIs that represent a major global health and socioeconomic burden.
机译:先天性免疫系统通过模式识别受体(PRR)来感应病原体,这些信号通过信号传导诱导效应细胞因子,例如Ⅰ型干扰素(IFN)。我们将IFN-ε表征为Ⅰ型IFN,是因为它通过Ifnarl和Ifnar2受体发出信号来诱导IFN调控的基因。与其他Ⅰ型IFN相比,已知的PRR途径不诱导IFN-ε。取而代之的是,IFN-ε在女性生殖道(FRT)的上皮细胞中组成性表达,并受到激素调节。 Ifn-ε缺陷型小鼠对普通性传播感染(STI)单纯疱疹病毒2和衣原体衣原体感染FRT的敏感性增加。因此,IFN-ε是有效的抗病原体和免疫调节细胞因子,在对抗代表重大全球健康和社会经济负担的性传播感染中可能很重要。

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  • 来源
    《Science》 |2013年第6123期|1088-1092|共5页
  • 作者单位

    Centre for Innate Immunity and Infectious Diseases, Monash Institute of Medical Research, Monash University, Clayton, Victoria, Australia;

    Centre for Innate Immunity and Infectious Diseases, Monash Institute of Medical Research, Monash University, Clayton, Victoria, Australia;

    Centre for Innate Immunity and Infectious Diseases, Monash Institute of Medical Research, Monash University, Clayton, Victoria, Australia;

    Centre for Asthma and Respiratory Disease and Hunter Medical Research Institute, The University of Newcastle, Newcastle, New South Wales, Australia;

    Centre for Asthma and Respiratory Disease and Hunter Medical Research Institute, The University of Newcastle, Newcastle, New South Wales, Australia;

    Centre for Innate Immunity and Infectious Diseases, Monash Institute of Medical Research, Monash University, Clayton, Victoria, Australia;

    Centre for Innate Immunity and Infectious Diseases, Monash Institute of Medical Research, Monash University, Clayton, Victoria, Australia;

    Centre for Innate Immunity and Infectious Diseases, Monash Institute of Medical Research, Monash University, Clayton, Victoria, Australia,Department of Biochemistry and Molecular Biology, Monash University, Clayton, Victoria, Australia;

    Department of Biochemistry and Molecular Biology, Monash University, Clayton, Victoria, Australia;

    Robinson Institute and School of Paediatrics and Reproductive Health, University of Adelaide, South Australia, Australia;

    Robinson Institute and School of Paediatrics and Reproductive Health, University of Adelaide, South Australia, Australia;

    Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia,Sir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville, Australia;

    The Ritchie Centre, Monash Institute of Medical Research, Monash University, Clayton, Victoria, Australia,Department of Obstetrics and Gynaecology, Monash University, Clayton, Victoria, Australia;

    The Ritchie Centre, Monash Institute of Medical Research, Monash University, Clayton, Victoria, Australia;

    Department of Ophthalmology and Department of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA;

    Centre for Asthma and Respiratory Disease and Hunter Medical Research Institute, The University of Newcastle, Newcastle, New South Wales, Australia;

    Centre for Innate Immunity and Infectious Diseases, Monash Institute of Medical Research, Monash University, Clayton, Victoria, Australia;

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  • 入库时间 2022-08-18 02:52:48

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