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Reduced Frequency of Murine Cytomegalovirus Retinitis in C57BL/6 Mice Correlates with Low Levels of Suppressor of Cytokine Signaling (SOCS)1 and SOCS3 Expression within the Eye during Corticosteroid-Induced Immunosuppression

机译:皮质类固醇诱导的免疫抑制过程中C57BL / 6小鼠的小鼠巨细胞病毒性视网膜炎发生频率降低与细胞因子信号转导(SOCS)1和SOCS3表达的低水平抑制相关

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摘要

AIDS-related human cytomegalovirus retinitis remains a leading cause of blindness worldwide. We compared two C57BL/6 mouse models of experimental murine cytomegalovirus (MCMV) retinitis for intraocular expression of suppressors of cytokine signaling (SOCS)1 and SOCS3, host proteins that are inducible negative feedback regulators of cytokine signaling. These mouse models differed in method of immune suppression, one by retrovirus-induced immune suppression (MAIDS) and the other by corticosteroid-induced immune suppression. Following subretinal injection of MCMV to induce retinitis, intraocular SOCS1 and SOCS3 were only mildly stimulated, and often without significance, within MCMV-infected eyes during the progression of MCMV retinitis in corticosteroid-immunosuppressed mice, contrary to MCMV-infected eyes of mice with MAIDS that showed significant high stimulation of SOCS1 and SOCS3 expression in agreement with previous findings. Frequency and severity of retinitis as well as amounts of intraocular infectious MCMV in corticosteroid-immunosuppressed mice were also unexpectedly lower than values previously reported for MAIDS animals during MCMV retinitis. These data reveal a major difference between two mouse models of experimental MCMV retinitis and suggest a possible link between the amplitude of SOCS1 and SOCS3 stimulation and severity of disease in these models.
机译:艾滋病相关的人类巨细胞病毒性视网膜炎仍然是全世界失明的主要原因。我们比较了两种实验鼠巨细胞病毒(MCMV)视网膜炎的C57BL / 6小鼠模型眼内表达的细胞因子信号传导(SOCS)1和SOCS3抑制剂的表达,宿主蛋白是可诱导的细胞因子信号传导的负反馈调节剂。这些小鼠模型的免疫抑制方法不同,一种通过逆转录病毒诱导的免疫抑制(MAIDS),另一种通过皮质类固醇诱导的免疫抑制。视网膜下注射MCMV诱发视网膜炎后,在皮质类固醇免疫抑制小鼠的MCMV视网膜炎进展过程中,MCMV感染的眼睛仅对眼内的SOCS1和SOCS3轻度刺激,并且通常没有意义,这与MAIDS小鼠的MCMV感染的眼睛相反与以前的发现一致,表明对SOCS1和SOCS3表达的显着高刺激。皮质类固醇免疫抑制小鼠的视网膜炎的频率和严重程度以及眼内感染性MCMV的量也出乎意料地低于先前在MCMV视网膜炎期间MAIDS动物的报道值。这些数据揭示了实验MCMV视网膜炎的两种小鼠模型之间的主要差异,并暗示了在这些模型中,SOCS1和SOCS3刺激的幅度与疾病严重程度之间可能存在联系。

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