Cited by 187Immunotherapy and Immune ResponsesImmune responses and vaccinationsT-cell and B-cell Immunology

Loss of Phagocytic and Antigen Cross-Presenting Capacity in Aging Dendritic Cells Is Associated with Mitochondrial Dysfunction

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Chougnet, Claire A, Thacker, Robert I, Shehata, Hesham M, Hennies, Cassandra M, Lehn, Maria A, Lages, Celine S, Janssen, Edith M·2015·The Journal of Immunology

Abstract

Impaired functionality of dendritic cells (DCs) significantly contributes to decreased adaptive immune responses in aged hosts. The expression of MHC-peptide on the DC surface is the critical first step in T cell priming, but few studies have addressed the effect of aging on Ag acquisition, processing, and presentation by DCs. In this study, we show that aged murine DCs were less efficient in the cross-presentation of cell-associated Ag and subsequently in the cross-priming of CD8+ T cells than were their young counterparts. The decreased cross-presentation was associated with a reduction in the frequency of CD8α DCs and merocytic (CD8α−CD11b−)DCs that could endocytose cell-associated Ag, as well as the number and the size of the endocytosed particles in the DC that did internalize cell-associated materials. Mechanistically, phagocytic capacity has been associated with mitochondrial activity and membrane potential (Δψm). Aged DCs exhibited profound signs of mitochondrial dysfunction, illustrated by lower Δψm, reduced ATP turnover and coupling efficiency, decreased baseline oxidative phosphorylation, and greater proton leak and reactive oxygen species (ROS) production. Mimicking the aged metabolic phenotype in young DCs by pharmacologic manipulation indicated that the reductions in Δψm and ATP impeded the phagocytic capacity whereas ROS interfered with a later step in the cross-presentation process. Conversely, in vitro scavenging of ROS partially restored cross-presentation by aged DCs. Taken together, these data suggest that improvement of aged DC functionality might be feasible in the elderly by targeting metabolic dysfunction or its downstream sequelae, thereby opening new avenues for enhancing vaccine efficiency in this population.

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  • Many immune cell subsets become hyporesponsive to acute challenges with age.

    “Thus, many immune cell subsets become hyporesponsive to acute challenges as we age17,19-25.”

    From SARS-CoV-2, COVID-19 and the aging immune system (2021) · cites this paper as [19]

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  1. [39]Marchi S Giorgi C Suski JM Agnoletto C Bononi A Bonora M De Marchi E Missiroli S Patergnani S Poletti F Rimessi A Duszynski J Wieckowski MR Pinton P 2011 Mitochondria-ros crosstalk in the control of cell death and aging J Signal Transduct 2012 329635 22175013 PMC3235816

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Authors
Chougnet, C. A., Thacker, R. I., Shehata, H. M., Hennies, C. M., Lehn, M. A., Lages, C. S., & Janssen, E. M.
Affiliations
Cincinnati Children's Hospital Medical Center (US)
Venue
The Journal of Immunology
Published
2015-09
Volume
195
Issue
6
Pages
2624-2632
ISSN
  • 0022-1767 (ISSN-L)
  • 1550-6606
OpenAlex
W1912751031
Cited by
187
References
58
Citations by year
2026: 20 · 2025: 24 · 2024: 21 · 2023: 16 · 2022: 23 · 2021: 23 · 2020: 17 · 2019: 19 · 2018: 7 · 2017: 12 · 2016: 5
FWCI
3.94
Type
journal article
Language
en
Open access
Locations
  • The Journal of Immunology (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • Ellison Medical Foundation
  • Cincinnati Children's Hospital Medical Center
  • National Institutes of Health
  • National Institute on Aging (AG033057, R01AG033057, R56AG033057)
  • National Cancer Institute (R01CA138617, CA138617)
  • National Institute of Arthritis and Musculoskeletal and Skin Diseases (P30AR047363, P30AR070549)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
  • Life Sciences › Immunology and Microbiology › Immunology › Immune responses and vaccinations
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
Keywords
cross-presentation, phagocytosis, mitochondrial dysfunction, mitochondrial membrane potential, reactive oxygen species, CD8α+ dendritic cells, oxidative phosphorylation, ATP turnover, immunosenescence
MeSH terms
Immunosenescence, Animals, Cells, Cultured, Dendritic Cells, Mice, Inbred C57BL, Mitochondria, Ovalbumin, Oxidative Phosphorylation, Phagocytosis, Cellular Senescence, Reactive Oxygen Species, Antigen Presentation, CD8-Positive T-Lymphocytes, Cross-Priming, Mice, Adaptive Immunity

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