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马立克氏病病毒调节 T 细胞增殖 环氧化酶 2 依赖性前列腺素 E2 的激活。

Marek's Disease Virus Modulates T Cell Proliferation Activation of Cyclooxygenase 2-Dependent Prostaglandin E2.

机构信息

The Pirbright Institute, Woking, United Kingdom.

Department of Life Sciences, College of Health and Life Sciences, Brunel University, London, United Kingdom.

出版信息

Front Immunol. 2021 Dec 22;12:801781. doi: 10.3389/fimmu.2021.801781. eCollection 2021.

Abstract

Marek's disease virus (MDV), an avian alphaherpesvirus, infects chickens, transforms CD4+ T cells, and induces immunosuppression early during infection. However, the exact mechanisms involved in MDV-induced immunosuppression are yet to be identified. Here, our results demonstrate that MDV infection and induces activation of cyclooxygenase-2 (COX-2) and production of prostaglandin E2 (PGE2). This exerts its inhibitory effects on T cell proliferation at day 21 post infection PGE2 receptor 2 (EP2) and receptor 4 (EP4). Impairment of the MDV-induced T cell proliferation was associated with downregulation of IL-2 and transferrin uptake in a COX-2/PGE2 dependent manner . Interestingly, oral administration of a COX-2 inhibitor, meloxicam, during MDV infection inhibited COX-2 activation and rescued T cell proliferation at day 21 post infection. Taken together, our results reveal a novel mechanism that contributes to immunosuppression in the MDV-infected chickens.

摘要

马立克氏病病毒(MDV)是一种禽α疱疹病毒,感染鸡,在感染早期转化 CD4+T 细胞并诱导免疫抑制。然而,MDV 诱导免疫抑制的确切机制仍有待确定。在这里,我们的结果表明,MDV 感染和诱导环氧化酶-2(COX-2)的激活和前列腺素 E2(PGE2)的产生。这在感染后第 21 天对 T 细胞增殖产生抑制作用,PGE2 受体 2(EP2)和受体 4(EP4)。COX-2/PGE2 依赖性下调白细胞介素 2 和转铁蛋白摄取与 MDV 诱导的 T 细胞增殖受损有关。有趣的是,在 MDV 感染期间口服 COX-2 抑制剂美洛昔康可抑制 COX-2 的激活,并在感染后第 21 天挽救 T 细胞增殖。总之,我们的研究结果揭示了一种新的机制,有助于 MDV 感染鸡的免疫抑制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ce0/8727754/052bcfda4983/fimmu-12-801781-g001.jpg

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