免疫系统
免疫学
CD40
先天免疫系统
细胞因子
干扰素
单核细胞
下调和上调
信号转导
生物
细胞生物学
抗原
细胞毒性T细胞
体外
基因
遗传学
作者
Jennifer Connors,David Joyner,Nathan Mege,Gina Cusimano,Matthew R. Bell,Jennifer Marcy,Bhavani Taramangalam,Kenneth M. Kim,Paulo J.C. Lin,Ying K. Tam,Drew Weissman,Michele A. Kutzler,Mohamad‐Gabriel Alameh,Elias K. Haddad
标识
DOI:10.1038/s42003-023-04555-1
摘要
Abstract Herein, we studied the impact of empty LNP (eLNP), component of mRNA-based vaccine, on anti-viral pathways and immune function of cells from young and aged individuals. eLNP induced maturation of monocyte derived dendritic cells (MDDCs). We further show that eLNP upregulated CD40 and induced cytokine production in multiple DC subsets and monocytes. This coincided with phosphorylation of TANK binding kinase 1 (pTBK1) and interferon response factor 7 (pIRF7). In response to eLNP, healthy older adults (>65 yrs) have decreased CD40 expression, and IFN-γ output compared to young adults (<65 yrs). Additionally, cells from older adults have a dysregulated anti-viral signaling response to eLNP stimulation, measured by the defect in type I IFN production, and phagocytosis. Overall, our data show function of eLNP in eliciting DC maturation and innate immune signaling pathways that is impaired in older adults resulting in lower immune responses to SARS-CoV-2 mRNA-based vaccines.
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