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A SOCS1/3 Antagonist Peptide Protects Mice Against Lethal Infection with Influenza A Virus

机译:SOCS1 / 3拮抗剂肽可保护小鼠免受甲型流感病毒的致死性感染。

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摘要

We have developed an antagonist to suppressor of cytokine signaling 1 (SOCS1), pJAK2(1001–1013), which corresponds to the activation loop of the Janus kinase JAK2, which is the binding site for the kinase inhibitory region (KIR) of SOCS1. Internalized pJAK2(1001–1013) inhibits SOCS1 and SOCS3. SOCS1 has been shown to be an influenza virus-induced virulence factor that enhances infection of cells. The antagonist was protective in cell culture and in influenza virus PR8 lethally infected C57BL/6 mice. The SOCS antagonist also prevented adverse morbidity as assessed by parameters, such as weight loss and drop in body temperature, and showed potent induction of both the cellular and humoral immune responses to the influenza virus candidate universal antigen matrix protein 2 (M2e). The SOCS antagonist, thus, protected mice against lethal influenza virus infection and possessed potent adjuvancy against the M2e candidate influenza virus universal vaccine antigen.
机译:我们已经开发了一种抑制细胞因子信号传导1(SOCS1)的拮抗剂pJAK2(1001–1013),它对应于Janus激酶JAK2的激活环,该激活环是SOCS1激酶抑制区(KIR)的结合位点。内在的pJAK2(1001–1013)会抑制SOCS1和SOCS3。已经证明SOCS1是流感病毒诱导的增加细胞感染的毒力因子。该拮抗剂在细胞培养中和在致命感染流感病毒PR8的C57BL / 6小鼠中具有保护作用。 SOCS拮抗剂还可以通过参数(例如体重减轻和体温下降)评估预防不良发病率,并显示出对流感病毒候选通用抗原基质蛋白2(M2e)的细胞和体液免疫应答的有效诱导。因此,SOCS拮抗剂可以保护小鼠免受致命的流感病毒感染,并具有针对M2e候选流感病毒通用疫苗抗原的强效佐剂。

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