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The frequency of interleukin-1β-producing monocytes is significantly associated with varicella-zoster responses of nursing home residents
Abstract
Summary: Previous studies have demonstrated that the status of the T cell compartment and inflammation-related factors are associated with the immunogenicity of the varicella-zoster virus (VZV) vaccine in older adults; however, little is known about the roles of other immune cell subsets known to influence the generation and maintenance of immunological memory. Responses to a live-attenuated VZV vaccine were studied in relation to peripheral blood mononuclear cell (PBMC) composition and function in a sample of 30 nursing home residents (aged 80–99 years). Interferon-gamma enzyme-linked immunospot (ELISPOT) was used to measure VZV responses at baseline and 6 weeks following vaccination, and associations were sought with the frequencies of monocytes and T, B and natural killer (NK) cells and the production and secretion of cytokines following their ex-vivo stimulation with different agents. While only the frequency of interleukin (IL)-6+ CD14+ monocytes was inversely associated with post-vaccination VZV response, amounts of IL-1β, IL-10, IL-17A and tumour necrosis factor (TNF) secreted by PBMCs and the frequency of IL-1β+ CD14+ monocytes was positively correlated with pre-vaccination VZV response. Furthermore, both bivariate correlation and causal mediation analyses supported the notion that IL-1β+ CD14+ monocytes were significant mediators of the associations between IL-1β and TNF secretion by PBMCs and pre-vaccination VZV responses. Our findings implicate a strong cytokine response mediated by inflammatory IL-1β+ monocytes in coordinating responses of long-lived VZV-reactive memory T cells, but with an opposing effect of IL-6+ CD14+ monocytes. Whether monocyte status promotes or inhibits the induction and/or maintenance of these memory T cells later in life has yet to be determined.
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“In a timecourse of ageing, mice overexpressing the proinflammatory molecule S100A9 develop increasing NLRP3 activation in bone marrow cells between 2 to 11 months of age 202 .”
From Clonal haematopoiesis and dysregulation of the immune system (2023) · cites this paper as [202]
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Cited by
Clonal haematopoiesis and dysregulation of the immune system
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Metadata
- Authors
- Picard, E., Bowdish, D. M. E., McElhaney, J. E., Pawelec, G., Loeb, M., & Verschoor, C. P.
- Affiliations
- Health Sciences North Research Institute, Sudbury, ON, Canada
- Department of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada
- ORCID
- Picard, E
- Venue
- Clinical and Experimental Immunology
- Publisher
- Oxford University Press (OUP)
- Published
- 2021-04-04
- Volume
- 205
- Issue
- 1
- Pages
- 63-74
- ISSN
- 0009-9104
- 1365-2249
- Cited by
- 3
- References
- 48
- Language
- en
- Licence
- academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model (vor)
- Funders
- Health Sciences North
- McMaster University
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