The Pirbright Institute, Woking, United Kingdom.
Department of Life Sciences, College of Health and Life Sciences, Brunel University, London, United Kingdom.
Front Immunol. 2021 Dec 22;12:801781. doi: 10.3389/fimmu.2021.801781. eCollection 2021.
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.
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。