Influenza-Induced Production of Interferon-Alpha is Defective in Geriatric Individuals

被引:55
作者
Canaday, David H. [3 ,4 ]
Amponsah, Naa Ayele [3 ]
Jones, Leola [3 ]
Tisch, Daniel J. [2 ]
Hornick, Thomas R. [4 ]
Ramachandra, Lakshmi [1 ]
机构
[1] Case Western Reserve Univ, Dept Pathol, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Dept Epidemiol & Biostat, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Div Infect Dis, Dept Med, Cleveland, OH 44106 USA
[4] Cleveland VA Med Ctr, GRECC, Cleveland, OH 44106 USA
关键词
Aging; influenza; interferon-alpha; plasmacytoid dendritic cells; PLASMACYTOID DENDRITIC CELLS; RESPIRATORY SYNCYTIAL VIRUS; DOUBLE-STRANDED-RNA; CD4(+) T-CELLS; I INTERFERON; RIG-I; IFN-ALPHA/BETA; ANTIVIRAL RESPONSES; CLONAL EXPANSION; BACTERIAL-DNA;
D O I
10.1007/s10875-010-9374-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The majority of deaths (90%) attributed to influenza are in person's age 65 or older. Little is known about whether defects in innate immune responses in geriatric individuals contribute to their susceptibility to influenza. Our aim was to analyze interferon-alpha (IFN-alpha) production in peripheral blood mononuclear cells (PBMCs) isolated from young and geriatric adult donors, stimulated with influenza A or Toll-like receptor (TLR) ligands. IFN-alpha is a signature anti-viral cytokine that also shapes humoral and cell-mediated immune responses. Geriatric PBMCs produced significantly less IFN-alpha in response to live or inactivated influenza (a TLR7 ligand) but responded normally to CpG ODN (TLR9 ligand) and Guardiquimod (TLR7 ligand). All three ligands activate plasmacytoid dendritic cells (pDCs). While there was a modest decline in pDC frequency in older individuals, there was no defect in uptake of influenza by geriatric pDCs. Influenza-induced production of IFN-alpha was defective in geriatric PBMCs by a mechanism that was independent of reduced pDC frequency or viability, defects in uptake of influenza, inability to secrete IFN-alpha, or defects in TLR7 signaling.
引用
收藏
页码:373 / 383
页数:11
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