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Systems Analysis of Immunity to Influenza Vaccination across Multiple Years and in Diverse Populations Reveals Shared Molecular Signatures

机译:跨年度和不同人群的流感疫苗免疫系统分析揭示了共享的分子特征

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Systems approaches have been used to describe molecular signatures driving immunity to influenza vaccination in humans. Whether such signatures are similar across multiple seasons and in diverse populations is unknown. We applied systems approaches to study immune responses in young, elderly, and diabetic subjects vaccinated with the seasonal influenza vaccine across five consecutive seasons. Signatures of innate immunity and plasmablasts correlated with and predicted influenza antibody titers at 1 month after vaccination with >80% accuracy across multiple seasons but were not associated with the longevity of the response. Baseline signatures of lymphocyte and monocyte inflammation were positively and negatively correlated, respectively, with antibody responses at 1 month. Finally, integrative analysis of microRNAs and transcriptomic profiling revealed potential regulators of vaccine immunity. These results identify shared vaccine-induced signatures across multiple seasons and in diverse populations and might help guide the development of next-generation vaccines that provide persistent immunity against influenza.
机译:系统方法已用于描述驱动人类对流感疫苗免疫的分子标记。这些特征在多个季节和不同人群中是否相似尚不清楚。我们应用系统方法研究了连续五个季节接种季节性流感疫苗的年轻人,老年人和糖尿病患者的免疫应答。先天免疫和成纤维细胞的特征与疫苗接种后1个月的流感抗体滴度相关,并在多个季节中以> 80%的准确性进行预测,但与反应的持续时间无关。 1个月时,淋巴细胞和单核细胞炎症的基线特征分别与抗体反应呈正相关和负相关。最后,对microRNA和转录组分析的综合分析揭示了疫苗免疫的潜在调节剂。这些结果确定了多个季节和不同人群中共享的疫苗诱导特征,并且可能有助于指导提供对流感持续免疫的下一代疫苗的开发。

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