Publication | Open Access
Prolonged Proinflammatory Cytokine Production in Monocytes Modulated by Interleukin 10 After Influenza Vaccination in Older Adults
67
Citations
26
References
2014
Year
Innate Immune SystemImmunologyImmune RegulationImmunologic MechanismCd4 T Cell ResponsesInnate ImmunityFlu VaccinationImmune SystemImmune DysregulationInflammationClassical Cd14Immune MediatorImmunological MemoryIl-10 ProductionChronic InflammationInterleukin 10Humoral ImmunityT Cell ImmunityImmune FunctionCytokineImmune Effector FunctionsImmune Cell DevelopmentInflammatory MonocytesInflammation BiologyInfluenza VaccinationOlder AdultsMedicineViral Immunity
We evaluated in vivo innate immune responses in monocyte populations from 67 young (aged 21-30 years) and older (aged ≥65 years) adults before and after influenza vaccination. CD14(+)CD16(+) inflammatory monocytes were induced after vaccination in both young and older adults. In classical CD14(+)CD16(-) and inflammatory monocytes, production of tumor necrosis factor α and interleukin 6, as measured by intracellular staining, was strongly induced after vaccination. Cytokine production was strongly associated with influenza vaccine antibody response; the highest levels were found as late as day 28 after vaccination in young subjects and were substantially diminished in older subjects. Notably, levels of the anti-inflammatory cytokine interleukin 10 (IL-10) were markedly elevated in monocytes from older subjects before and after vaccination. In purified monocytes, we found age-associated elevation in phosphorylated signal transducer and activator of transcription-3, and decreased serine 359 phosphorylation of the negative IL-10 regulator dual-specificity phosphatase 1. These findings for the first time implicate dysregulated IL-10 production in impaired vaccine responses in older adults.
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