Loss of Phagocytic and Antigen Cross-Presenting Capacity in Aging Dendritic Cells Is Associated with Mitochondrial Dysfunction
Open accessAbstract
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.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
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]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Cross-presentation by dendritic cells
Joffre, O. P., Segura, É., Savina, A., & Amigorena, S. (2012) · Nature reviews. Immunology · doi:10.1038/nri3254 · Cited by 1,646 · see citing works
CD4+ T cells are required for secondary expansion and memory in CD8+ T lymphocytes
Janssen, E. M., Lemmens, E. E., Wolfe, T., Christen, U., von Herrath, M. G., & Schoenberger, S. P. (2003) · Nature · doi:10.1038/nature01441 · Cited by 1,635 · see citing works
Self-citationThe role of mitochondria in aging
Bratic, A., & Larsson, N.-G. (2013) · Journal of Clinical Investigation · doi:10.1172/jci64125 · Cited by 1,087 · see citing works
Jongbloed, S. L., Kassianos, A. J., McDonald, K. J., Clark, G. J., Ju, X., Angel, C. E., Chen, C. J., Dunbar, P. R., Wadley, R. B., Jeet, V., et al. (2010) · The Journal of Experimental Medicine · doi:10.1084/jem.20092140 · Cited by 1,019 · see citing works
Savina, A., Jancic, C. C., Hugues, S., Guermonprez, P., Vargas, P., Moura, I. C., Lennon‐Duménil, A., Seabra, M. C., Raposo, G., & Amigorena, S. (2006) · Cell · doi:10.1016/j.cell.2006.05.035 · Cited by 896 · see citing works
Aging of the innate immune system
Shaw, A. C., Joshi, S., Greenwood, H., Panda, A., & Lord, J. M. (2010) · Current Opinion in Immunology · doi:10.1016/j.coi.2010.05.003 · Cited by 647 · see citing works
The mitochondrial energy transduction system and the aging process
Navarro, A., & Boveris, A. (2007) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00213.2006 · Cited by 646 · see citing works
Mitochondria-Ros Crosstalk in the Control of Cell Death and Aging
Marchi, S., Giorgi, C., Suski, J. M., Agnoletto, C., Bononi, A., Bonora, M., Marchi, E. D., Missiroli, S., Patergnani, S., Poletti, F., et al. (2011) · Journal of Signal Transduction · doi:10.1155/2012/329635 · Cited by 639 · see citing works
CD4+ T-cell help controls CD8+ T-cell memory via TRAIL-mediated activation-induced cell death
Janssen, E. M., Droin, N. M., Lemmens, E. E., Pinkoski, M. J., Bensinger, S. J., Ehst, B. D., Griffith, T. S., Green, D. R., & Schoenberger, S. P. (2005) · Nature · doi:10.1038/nature03337 · Cited by 619 · see citing works
Self-citationAntigen-presentation properties of plasmacytoid dendritic cells.
Villadangos, J., & Young, L. J. (2008) · Immunity · doi:10.1016/j.immuni.2008.09.002 · Cited by 577 · see citing works
Panda, A., Qian, F., Mohanty, S., van Duin, D., Newman, F. K., Zhang, L., Chen, S., Towle, V., Belshe, R. B., Fikrig, E., et al. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0901022 · Cited by 548 · see citing works
Robbins, S. H., Walzer, T., Dembélé, D., Thibault-Carpentier, C., Defays, A., Bessou, G., Xu, H., Vivier, É., Sellars, M., Pierre, P., et al. (2008) · Genome biology · doi:10.1186/gb-2008-9-1-r17 · Cited by 534 · see citing works
New insights into the role of mitochondria in aging: mitochondrial dynamics and more
Seo, A. Y., Joseph, A.-M., Dutta, D., Hwang, J. C. Y., Aris, J. P., & Leeuwenburgh, C. (2010) · Journal of Cell Science · doi:10.1242/jcs.070490 · Cited by 522 · see citing works
Assessing bioenergetic function in response to oxidative stress by metabolic profiling
Dranka, B. P., Benavides, G. A., Diers, A. R., Giordano, S., Zelickson, B. R., Reily, C., Zou, L., Chatham, J. C., Hill, B. G., Zhang, J., et al. (2011) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2011.08.005 · Cited by 436 · see citing works
Agrawal, A., Agrawal, S., Cao, J.-N., Su, H., Osann, K., & Gupta, S. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.11.6912 · Cited by 435 · see citing works
Innate immunity in aging: impact on macrophage function
Plowden, J., Renshaw‐Hoelscher, M., Engleman, C., Katz, J. M., & Sambhara, S. R. (2004) · Aging Cell · doi:10.1111/j.1474-9728.2004.00102.x · Cited by 430 · see citing works
Karttunen, J. T., Sanderson, S., & Shastri, N. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.13.6020 · Cited by 420 · see citing works
Calcium signaling around Mitochondria Associated Membranes (MAMs)
Patergnani, S., Suski, J. M., Agnoletto, C., Bononi, A., Bonora, M., Marchi, E. D., Giorgi, C., Marchi, S., Missiroli, S., Poletti, F., et al. (2011) · Cell Communication and Signaling · doi:10.1186/1478-811x-9-19 · Cited by 410 · see citing works
Mitochondrial membrane potential and aging
Nicholls, D. G. (2003) · Aging Cell · doi:10.1111/j.1474-9728.2003.00079.x · Cited by 347 · see citing works
Studying the mononuclear phagocyte system in the molecular age
Chow, A. T., Brown, B. D., & Mérad, M. (2011) · Nature reviews. Immunology · doi:10.1038/nri3087 · Cited by 315 · see citing works
Jing, Y., Shaheen, E., Drake, R. R., Chen, N., Gravenstein, S., & Deng, Y. (2009) · Human Immunology · doi:10.1016/j.humimm.2009.07.005 · Cited by 284 · see citing works
Continued clearance of apoptotic cells critically depends on the phagocyte Ucp2 protein
Park, D., Han, C. Z., Elliott, M. R., Kinchen, J. M., Trampont, P. C., Das, S., Collins, S., Lysiak, J. J., Hoehn, K. L., & Ravichandran, K. S. (2011) · Nature · doi:10.1038/nature10340 · Cited by 248 · see citing works
Intracellular mechanisms of antigen cross presentation in dendritic cells
Amigorena, S., & Savina, A. (2010) · Current Opinion in Immunology · doi:10.1016/j.coi.2010.01.022 · Cited by 246 · see citing works
Mitochondrial protein quality control during biogenesis and aging
Baker, B. M., & Haynes, C. M. (2011) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2011.01.004 · Cited by 192 · see citing works
Crozat, K., Guiton, R., Guilliams, M., Henri, S., Baranek, T., Schwartz-Cornil, I., MALISSEN, B., & Dalod, M. (2010) · Immunological Reviews · doi:10.1111/j.0105-2896.2009.00868.x · Cited by 185 · see citing works
Aging impairs peritoneal but not bone marrow‐derived macrophage phagocytosis
Linehan, E., Dombrowski, Y., Snoddy, R., Fallon, P. G., Kissenpfennig, A., & Fitzgerald, D. C. (2014) · Aging Cell · doi:10.1111/acel.12223 · Cited by 169 · see citing works
Calcium dysregulation in neuronal aging and Alzheimer's disease: history and new directions
Thibault, O., Porter, N. M., Chen, K.-C., Blalock, E. M., Kaminker, P. G., Clodfelter, G. V., Brewer, L. D., & Landfield, P. W. (1998) · Cell Calcium · doi:10.1016/s0143-4160(98)90064-1 · Cited by 167 · see citing works
Impaired Dendritic Cell Function in Aging Leads to Defective Antitumor Immunity
Grolleau‐Julius, A., Harning, E. K., Close, L. A., & Yung, R. L. (2008) · Cancer Research · doi:10.1158/0008-5472.can-07-5769 · Cited by 151 · see citing works
Stout-Delgado, H. W., Yang, X. T., Walker, W. E., Tesar, B. M., & Goldstein, D. R. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.10.6747 · Cited by 148 · see citing works
Changes in the macrophage function with aging
la Fuente, M. D. (1985) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/0300-9629(85)90933-8 · Cited by 141 · see citing works
Partial restoration of T‐cell function in aged mice by in vitro blockade of the PD‐1/ PD‐L1 pathway
Lages, C. S., Lewkowich, I. P., Sproles, A. A., Wills-Karp, M. A., & Chougnet, C. A. (2010) · Aging Cell · doi:10.1111/j.1474-9726.2010.00611.x · Cited by 140 · see citing works
Self-citationImpact of aging on antigen presentation cell function of dendritic cells
Wong, C. K., & Goldstein, D. R. (2013) · Current Opinion in Immunology · doi:10.1016/j.coi.2013.05.016 · Cited by 129 · see citing works
Role of mitochondria and reactive oxygen species in dendritic cell differentiation and functions
Prete, A. D., Zaccagnino, P., Paola, M. D., Saltarella, M., Celis, C. O., Nico, B., Santoro, G., & Lorusso, M. P. (2008) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2007.12.037 · Cited by 119 · see citing works
Itoh, Y., Hemmer, B., Martinꝉ, R., & Germain, R. N. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.162.4.2073 · Cited by 114 · see citing works
Wei, Y., Wu, S., Ma, Y., & Lee, H. (2009) · PubMed · Cited by 113 · see citing works
Biology of Dendritic Cells in Aging
Agrawal, A., Agrawal, S., Tay, J., & Gupta, S. (2007) · Journal of Clinical Immunology · doi:10.1007/s10875-007-9127-6 · Cited by 112 · see citing works
The mitochondrial membrane potential and Ca2+ oscillations in smooth muscle
Chalmers, S., & McCarron, J. G. (2007) · Journal of Cell Science · doi:10.1242/jcs.014522 · Cited by 110 · see citing works
Gronski, M. A., Kinchen, J. M., Juncadella, I. J., Franc, N. C., & Ravichandran, K. S. (2009) · Cell Death & Differentiation · doi:10.1038/cdd.2009.55 · Cited by 92 · see citing works
Efficient T Cell Activation via a Toll-Interleukin 1 Receptor-Independent Pathway
Janssen, E. M., Tabeta, K., Barnes, M. J., Rutschmann, S., McBride, S. W., Bahjat, K. S., Schoenberger, S. P., Theofilopoulos, A. N., Beutler, B., & Hoebe, K. H. N. (2006) · Immunity · doi:10.1016/j.immuni.2006.03.024 · Cited by 91 · see citing works
Self-citationDendritic cells and aging: consequences for autoimmunity
Agrawal, A., Sridharan, A., Prakash, S., & Agrawal, H. (2011) · Expert Review of Clinical Immunology · doi:10.1586/eci.11.77 · Cited by 89 · see citing works
MacrophAging: A cellular and molecular review
Sebastián, C., Espia, M., Serra, M., Celada, A., & Lloberas, J. (2005) · Immunobiology · doi:10.1016/j.imbio.2005.05.006 · Cited by 88 · see citing works
Li, G., Smithey, M. J., Rudd, B. D., & Nikolich‐Žugich, J. (2012) · Aging Cell · doi:10.1111/j.1474-9726.2012.00867.x · Cited by 77 · see citing works
Pereira, L., de Souza, A. P. D., Borges, T. J., & Bonorino, C. (2011) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2011.03.005 · Cited by 77 · see citing works
Creatine kinase-mediated ATP supply fuels actin-based events in phagocytosis
Kuiper, J. W. P., Pluk, H., Oerlemans, F., van Leeuwen, F. N., de Lange, F., Fransen, J., & Wieringa, B. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060051 · Cited by 75 · see citing works
Wong, C. P., Magnusson, K. R., & Ho, E. (2009) · Experimental Gerontology · doi:10.1016/j.exger.2009.11.005 · Cited by 74 · see citing works
Tumor Antigen Cross‐Presentation and the Dendritic Cell: Where it All Begins?
McDonnell, A. M., Robinson, B. W. S., & Currie, A. J. (2010) · Journal of Immunology Research · doi:10.1155/2010/539519 · Cited by 70 · see citing works
Effect of Aging on Bone Marrow-Derived Murine CD11c+CD4-CD8 - Dendritic Cell Function
Grolleau‐Julius, A., Garg, M. R., Mo, R., Stoolman, L. L., & Yung, R. L. (2006) · The Journals of Gerontology Series A · doi:10.1093/gerona/61.10.1039 · Cited by 69 · see citing works
Elmezayen, R., Gazzar, M. E., Myer, R. G., & High, K. P. (2009) · Aging Cell · doi:10.1111/j.1474-9726.2009.00502.x · Cited by 54 · see citing works
Dendritic Cell Subsets in Type 1 Diabetes: Friend or Foe?
Morel, P. A. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00415 · Cited by 48 · see citing works
Effect of age on surface molecules and cytokine expression in human dendritic cells
Ciaramella, A., Spalletta, G., Bizzoni, F., Salani, F., Caltagirone, C., & Bossù, P. (2011) · Cellular Immunology · doi:10.1016/j.cellimm.2011.04.010 · Cited by 43 · see citing works
Cross-Presentation of Cell-Associated Antigens by Mouse Splenic Dendritic Cell Populations
Thacker, R. I., & Janssen, E. M. (2012) · Frontiers in Immunology · doi:10.3389/fimmu.2012.00041 · Cited by 41 · see citing works
Self-citationReboulet, R. A., Hennies, C. M., Garcia, Z., Nierkens, S., & Janssen, E. M. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1001619 · Cited by 39 · see citing works
Self-citationKatz, J. D., Ondr, J. K., Opoka, R. J., Garcia, Z., & Janssen, E. M. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1001398 · Cited by 36 · see citing works
Self-citationPhenotype and functions of conventional dendritic cells are not compromised in aged mice
Tan, S., Cavanagh, L. L., d'Advigor, W., Shackel, N. A., Groth, B. F. D. S., & Weninger, W. (2012) · Immunology and Cell Biology · doi:10.1038/icb.2011.104 · Cited by 32 · see citing works
Vaccine strategies to enhance immune responses in the aged
Lefebvre, J. S., & Haynes, L. (2013) · Current Opinion in Immunology · doi:10.1016/j.coi.2013.05.014 · Cited by 31 · see citing works
Mechanisms of murine dendritic cell antitumor dysfunction in aging
Grolleau‐Julius, A., Close, L. A., Harning, E. K., & Yung, R. L. (2008) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-008-0636-9 · Cited by 30 · see citing works
Guminska, M., Ptak, W., & Zembala, M. (2017) · Enzyme · doi:10.1159/000458969 · Cited by 24 · see citing works
Is cancer vaccination feasible at older age?
Gravekamp, C., & Jahangir, A. (2014) · Experimental Gerontology · doi:10.1016/j.exger.2014.01.025 · Cited by 8 · see citing works
Flagged first, then by citations
Research works printed but not linked: 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
Cited by
Sorted by citations
The twilight of immunity: emerging concepts in aging of the immune system
Nikolich-Žugich, J. (2018) · Nature Immunology · doi:10.1038/s41590-017-0006-x · Cited by 1,240 · see citing works
Targeting ROS in cancer: rationale and strategies
Glorieux, C., Liu, S., Trachootham, D., & Huang, P. (2024) · Nature Reviews Drug Discovery · doi:10.1038/s41573-024-00979-4 · Cited by 700 · see citing works
Can physical activity ameliorate immunosenescence and thereby reduce age-related multi-morbidity?
Duggal, N. A., Niemiro, G., Harridge, S. D. R., Simpson, R. J., & Lord, J. M. (2019) · Nature Reviews Immunology · doi:10.1038/s41577-019-0177-9 · Cited by 436 · see citing works
Cho, S. J., & Stout-Delgado, H. W. (2020) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021119-034610 · Cited by 458 · see citing works
Immune ageing at single-cell resolution
Mogilenko, D. A., Shchukina, I., & Artyomov, M. N. (2021) · Nature reviews. Immunology · doi:10.1038/s41577-021-00646-4 · Cited by 392 · see citing works
SARS-CoV-2, COVID-19 and the aging immune system
Bartleson, J. M., Radenkovic, D., Covarrubias, A. J., Furman, D., Winer, D. A., & Verdin, E. (2021) · Nature Aging · doi:10.1038/s43587-021-00114-7 · Cited by 359 · see citing works
Mitochondrial oxidative stress in the tumor microenvironment and cancer immunoescape: foe or friend?
Kuo, C., Babuharisankar, A. P., Lin, Y.-C., Lien, H.-W., Lo, Y.-K., Chou, H.-Y., Tangeda, V., Cheng, L.-C., Cheng, A., & Lee, A. (2022) · Journal of Biomedical Sciences · doi:10.1186/s12929-022-00859-2 · Cited by 316 · see citing works
The integration of inflammaging in age-related diseases
Fülöp, T., Witkowski, J. M., Olivieri, F., & Larbi, A. (2018) · Seminars in Immunology · doi:10.1016/j.smim.2018.09.003 · Cited by 356 · see citing works
The Confluence of Sex Hormones and Aging on Immunity
Gubbels Bupp, M. R., Potluri, T., Fink, A. L., & Klein, S. L. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01269 · Cited by 277 · see citing works
Immune System Dysfunction in the Elderly
Eduardo Fuentes, Q., FUENTES, M., Alarcón, M. A., & Palomo, I. F. (2017) · Anais da Academia Brasileira de Ciências · doi:10.1590/0001-3765201720160487 · Cited by 234 · see citing works
Metabolic Control of Dendritic Cell Functions: Digesting Information
Wculek, S. K., Khouili, S. C., Priego, E., Heras‐Murillo, I., & Sancho, D. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00775 · Cited by 212 · see citing works
Ageing of the gut microbiome: Potential influences on immune senescence and inflammageing
Conway, J., & Duggal, N. A. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101323 · Cited by 194 · see citing works
I mmunosenescence and Inflammaging: Risk Factors of Severe COVID-19 in Older People
Pietrobon, A. J., Teixeira, F. M. E., & Sato, M. N. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.579220 · Cited by 185 · see citing works
Age-related immune alterations and cerebrovascular inflammation
Finger, C. E., Moreno‐González, I., Gutiérrez, A., Moruno-Manchon, J. F., & McCullough, L. D. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01361-1 · Cited by 177 · see citing works
Roles of reactive oxygen species in inflammation and cancer
Yu, Y., Liu, S., Yang, L., Song, P., Liu, Z., Liu, X., Yan, X., & Dong, Q. (2024) · MedComm · doi:10.1002/mco2.519 · Cited by 170 · see citing works
Innate immune responses in the ageing lung.
Boe, D. M., Boule, L. A., & Kovacs, E. J. (2016) · Clinical and Experimental Immunology · doi:10.1111/cei.12881 · Cited by 156 · see citing works
Salminen, A., Kaarniranta, K., & Kauppinen, A. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03048-x · Cited by 156 · see citing works
Reactive Oxygen Species and Antitumor Immunity—From Surveillance to Evasion
Kotsafti, A., Scarpa, M., Castagliuolo, I., & Scarpa, M. (2020) · Cancers · doi:10.3390/cancers12071748 · Cited by 157 · see citing works
Brandenberger, C., & Mühlfeld, C. (2017) · Cell and Tissue Research · doi:10.1007/s00441-016-2511-x · Cited by 152 · see citing works
Immunosenescence and inflammaging: Mechanisms and role in diseases
Ajoolabady, A., Praticò, D., Tang, D., Zhou, S., Franceschi, C., & Ren, J. T. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102540 · Cited by 159 · see citing works
Immunosenescence: signaling pathways, diseases and therapeutic targets
Fu, Y., Wang, B., Alu, A., Hong, W., Hong, L., He, X., Shi, H., Cheng, P., & Yang, X. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02371-z · Cited by 157 · see citing works
Exercise immunology: Future directions
Nieman, D. C., & Pence, B. D. (2019) · Journal of sport and health science/Journal of Sport and Health Science · doi:10.1016/j.jshs.2019.12.003 · Cited by 147 · see citing works
Almanan, M., Raynor, J. L., Ogunsulire, I., Malyshkina, A., Mukherjee, S., Hummel, S. A., Ingram, J. T., Saini, A. S., Xie, M. M., Alenghat, T., et al. (2020) · Science Advances · doi:10.1126/sciadv.abb0806 · Cited by 125 · see citing works
Self-citationAging impairs mitochondrial respiratory capacity in classical monocytes
Pence, B. D., & Yarbro, J. R. (2018) · Experimental Gerontology · doi:10.1016/j.exger.2018.04.008 · Cited by 120 · see citing works
“2016) and dendritic cells (Chougnet et al. 2015), but results from these studies are limited in their focus on specific disease states, and mitochondrial function has not been investigated in monocytes.”
Salminen, A. (2021) · Journal of Molecular Medicine · doi:10.1007/s00109-021-02123-w · Cited by 124 · see citing works
Age-associated alterations in immune function and inflammation
Lewis, E. D., Wu, D., & Meydani, S. N. (2022) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2022.110576 · Cited by 111 · see citing works
Mitophagy plays a central role in mitochondrial ageing
Diot, A., Morten, K., & Poulton, J. (2016) · Mammalian Genome · doi:10.1007/s00335-016-9651-x · Cited by 109 · see citing works
Mitochondrial Dysfunction in Pulmonary Fibrosis
Rangarajan, S., Bernard, K. F., & Thannickal, V. J. (2017) · Annals of the American Thoracic Society · doi:10.1513/annalsats.201705-370aw · Cited by 107 · see citing works
Immunosenescence in multiple sclerosis: the identification of new therapeutic targets
Dema, M. G., Eixarch, H., Villar, L. M., Montalbán, X., & Espejo, C. (2021) · Autoimmunity Reviews · doi:10.1016/j.autrev.2021.102893 · Cited by 101 · see citing works
“Inflamm‐aging” influences immune cell survival factors in human bone marrow
Pangrazzi, L., Meryk, A., Naismith, E., Kozieł, R., Lair, J., Krismer, M., Trieb, K., & Grubeck‐Loebenstein, B. (2016) · European Journal of Immunology · doi:10.1002/eji.201646570 · Cited by 100 · see citing works
Reactive Oxygen Species in Autoimmune Cells: Function, Differentiation, and Metabolism
Lin, W., Shen, P., Song, Y., Huang, Y., & Tu, S. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.635021 · Cited by 97 · see citing works
Thomas, A. L., Lehn, M. A., Janssen, E. M., Hildeman, D. A., & Chougnet, C. A. (2022) · Scientific Reports · doi:10.1038/s41598-022-21920-y · Cited by 94 · see citing works
Self-citationVaena, S., Chakraborty, P., Lee, H. G., Janneh, A. H., Kassir, M. F., Beeson, G., Hedley, Z., Yalcinkaya, A., Sofi, M. H., Li, H., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109076 · Cited by 92 · see citing works
Reactive oxygen species and immune regulation
Zhou, Y., Min, Z., & Yu, B. (2020) · International Reviews of Immunology · doi:10.1080/08830185.2020.1768251 · Cited by 91 · see citing works
Zhang, F., Guo, J., Yu, S., Zheng, Y., Duan, M., Zhao, L., Wang, Y., Yang, Z., & Jiang, X. (2024) · 癌症:英文版 · doi:10.1002/cac2.12591 · Cited by 93 · see citing works
Oxygen in the tumor microenvironment: effects on dendritic cell function
Paardekooper, L. M., de Vos, W., & van den Bogaart, G. (2019) · Oncotarget · doi:10.18632/oncotarget.26608 · Cited by 87 · see citing works
Keilich, S. R., Bartley, J. M., & Haynes, L. (2019) · Cellular Immunology · doi:10.1016/j.cellimm.2019.103992 · Cited by 88 · see citing works
Oshi, M., Gandhi, S., Yan, L., Tokumaru, Y., Wu, R., Yamada, A., Matsuyama, R., Endo, I., & Takabe, K. (2022) · Breast Cancer Research and Treatment · doi:10.1007/s10549-022-06633-0 · Cited by 88 · see citing works
Multifaceted mitochondria in innate immunity
Marques, E., Kramer, R., & Ryan, D. G. (2024) · npj Metabolic Health and Disease · doi:10.1038/s44324-024-00008-3 · Cited by 88 · see citing works
Mitochondrial quality control in AMD: does mitophagy play a pivotal role?
Hyttinen, J. M. T., Viiri, J., Kaarniranta, K., & Błasiak, J. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-018-2843-7 · Cited by 78 · see citing works
Yarbro, J. R., Emmons, R. S., & Pence, B. D. (2020) · Immunometabolism · doi:10.20900/immunometab20200026 · Cited by 80 · see citing works
Implications of the Immune Landscape in COPD and Lung Cancer: Smoking Versus Other Causes
Taucher, E., Mykoliuk, I., Lindenmann, J., & Smolle-Jüettner, F.-M. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.846605 · Cited by 79 · see citing works
Reactive oxygen species in immune cells: A new antitumor target
Wang, L., Kuang, Z., Zhang, D., Gao, Y., Ying, M., & Wang, T. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110978 · Cited by 78 · see citing works
Lian, J., Liang, Y., Zhang, H., Lan, M., Ye, Z., Lin, B., Qiu, X., & Zeng, J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.912279 · Cited by 73 · see citing works
The Contribution of Oxidative Stress and Inflamm-Aging in Human and Equine Asthma
Bullone, M., & Lavoie, J. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18122612 · Cited by 72 · see citing works
Age-Related Changes in Thymic Central Tolerance
Srinivasan, J., Lancaster, J. N., Singarapu, N., Hale, L. P., Ehrlich, L. I. R., & Richie, E. R. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.676236 · Cited by 67 · see citing works
Exploring the Relationship between the Gut Microbiota and Ageing: A Possible Age Modulator
Salazar, J., Durán, P., Díaz, M. P., Chacín, M., Santeliz, R., Mengual, E., Gutiérrez, E., León, X., Díaz, A., Bernal, M., et al. (2023) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph20105845 · Cited by 71 · see citing works
Human bone marrow adipocytes display distinct immune regulatory properties
Miggitsch, C., Meryk, A., Naismith, E., Pangrazzi, L., Ejaz, A., Jenewein, B., Wagner, S., Nägele, F., Fenkart, G., Trieb, K., et al. (2019) · EBioMedicine · doi:10.1016/j.ebiom.2019.07.023 · Cited by 71 · see citing works
Tumor microenvironment-related dendritic cell deficiency: a target to enhance tumor immunotherapy
Zhu, S., Yang, N., Wu, J., Wang, X., Wang, W., Liu, Y.-J., & Chen, J. (2020) · Pharmacological Research · doi:10.1016/j.phrs.2020.104980 · Cited by 71 · see citing works
Immunosenescence, Inflammaging, and Lung Senescence in Asthma in the Elderly
Soma, T., & Nagata, M. (2022) · Biomolecules · doi:10.3390/biom12101456 · Cited by 71 · see citing works
Aging, cancer, and antitumor immunity
Ikeda, H., & Togashi, Y. (2021) · International Journal of Clinical Oncology · doi:10.1007/s10147-021-01913-z · Cited by 65 · see citing works
Immune Cell Number, Phenotype, and Function in the Elderly with Sepsis
He, W., Xiao, K., Fang, M., & Xie, L. (2021) · Aging and Disease · doi:10.14336/ad.2020.0627 · Cited by 65 · see citing works
Immunosenescence and inflamm-ageing in COVID-19
Zinatizadeh, M. R., Zarandi, P. K., Ghiasi, M., Kooshki, H., Mohammadi, M., Amani, J., & Rezaei, N. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101818 · Cited by 62 · see citing works
Roles of DNA repair enzyme OGG1 in innate immunity and its significance for lung cancer
Vlahopoulos, S., Adamaki, M., Khoury, N., Zoumpourlis, V. C., & Boldogh, I. R. (2018) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2018.09.004 · Cited by 65 · see citing works
Relationships Between Ion Channels, Mitochondrial Functions and Inflammation in Human Aging
Strickland, M., Yacoubi‐Loueslati, B., Bouhaouala‐Zahar, B., Pender, S. L. F., & Larbi, A. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00158 · Cited by 63 · see citing works
Perdaens, O., & Pesch, V. V. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2021.811518 · Cited by 59 · see citing works
Targeting Immune Senescence in Atherosclerosis
Vellasamy, D. M., Lee, S.-J., Goh, K. W., Goh, B. H., Tang, Y.-Q., Ming, L. C., & Yap, W. H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113059 · Cited by 60 · see citing works
Metabolic regulation of dendritic cell activation and immune function during inflammation
Wu, L., Yan, Z., Jiang, Y., Chen, Y., Du, J., Guo, L., Xu, J., Luo, Z., & Liu, Y. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1140749 · Cited by 62 · see citing works
Mitochondrial dynamics and metabolism across skin cells: implications for skin homeostasis and aging
Martic, I., Papaccio, F., Bellei, B., & Cavinato, M. S. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1284410 · Cited by 57 · see citing works
Zhang, P., Catterson, J. H., Grönke, S., & Partridge, L. (2024) · Nature Aging · doi:10.1038/s43587-024-00578-3 · Cited by 60 · see citing works
Reversing the immune ageing clock: lifestyle modifications and pharmacological interventions
Duggal, N. A. (2018) · Biogerontology · doi:10.1007/s10522-018-9771-7 · Cited by 53 · see citing works
Liu, Q., Li, J., Sun, X., Lin, J., Yu, Z., Xiao, Y., Li, D., Sun, B., Bao, H., & Liu, Y. (2025) · Journal of Hematology & Oncology · doi:10.1186/s13045-025-01735-w · Cited by 54 · see citing works
Potential Benefits of Antioxidant Phytochemicals in Type 2 Diabetes
Arabshomali, A., Bazzazzadehgan, S., Mahdi, F., & Shariat‐Madar, Z. (2023) · Molecules · doi:10.3390/molecules28207209 · Cited by 50 · see citing works
Reactive oxygen species associated immunoregulation post influenza virus infection
Wang, L., Cao, Z., Wang, Z., Guo, J., & Wen, J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.927593 · Cited by 49 · see citing works
Immune Alterations with Aging: Mechanisms and Intervention Strategies
Yu, W., Yu, Y., Sun, S., Lu, C., Zhai, J., Lei, Y., Bai, F., Wang, R., & Chen, J. (2024) · Nutrients · doi:10.3390/nu16223830 · Cited by 51 · see citing works
Shaping of Dendritic Cell Function by the Metabolic Micro-Environment
Brombacher, E. C., & Everts, B. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.00555 · Cited by 47 · see citing works
Cellular senescence in cancer: molecular mechanisms and therapeutic targets
Jin, P., Duan, X., Li, L., Zhou, P., Zou, C., & Xie, K. (2024) · MedComm · doi:10.1002/mco2.542 · Cited by 46 · see citing works
Gardner, J. K., Mamotte, C. D. S., Jackaman, C., & Nelson, D. J. (2017) · Ageing Research Reviews · doi:10.1016/j.arr.2017.07.002 · Cited by 40 · see citing works
Adamik, J., Munson, P. V., Maurer, D. M., Hartmann, F. J., Bendall, S. C., Argüello, R. J., & Butterfield, L. H. (2023) · Nature Communications · doi:10.1038/s41467-023-42881-4 · Cited by 40 · see citing works
Rondão, C., Mota, M. P., Oliveira, M. M., Peixoto, F., & Esteves, D. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.950937 · Cited by 37 · see citing works
Cellular Senescence in Immunity against Infections
Marrella, V., Facoetti, A., & Cassani, B. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231911845 · Cited by 37 · see citing works
Implications of inflammatory states on dysfunctional immune responses in aging and obesity
Thomas, A. L., Alarcon, P. C., Divanovic, S., Chougnet, C. A., Hildeman, D. A., & Moreno-Fernandez, M. E. (2021) · Frontiers in Aging · doi:10.3389/fragi.2021.732414 · Cited by 35 · see citing works
Self-citationEnhancing immunity during ageing by targeting interactions within the tissue environment
Bracken, O. V., Maeyer, R. P. H. D., & Akbar, A. N. (2025) · Nature Reviews Drug Discovery · doi:10.1038/s41573-024-01126-9 · Cited by 40 · see citing works
Rahmatpanah, F. B., Agrawal, S., Scarfone, V. M., Kapadia, S., Mercola, D., & Agrawal, A. (2018) · The Journals of Gerontology Series A · doi:10.1093/gerona/gly106 · Cited by 34 · see citing works
Effects of cellular senescence on metabolic pathways in non-immune and immune cells
Frasca, D., Saada, Y. B., Garcia, D., & Friguet, B. (2020) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2020.111428 · Cited by 34 · see citing works
Liang, W., He, X., Bi, J., Hu, T., & Sun, Y. (2021) · Oncology Reports · doi:10.3892/or.2021.8159 · Cited by 33 · see citing works
Metabolic guidance and stress in tumors modulate antigen-presenting cells
Park, J., Wang, L., & Ho, P. (2022) · Oncogenesis · doi:10.1038/s41389-022-00438-y · Cited by 33 · see citing works
Genomic programming of IRF4-expressing human Langerhans cells
Sirvent, S., Vallejo, A. F., Davies, J., Clayton, K., Wu, Z., Woo, J., Riddell, J., Chaudhri, V. K., Stumpf, P. S., Nazlamova, L., et al. (2020) · Nature Communications · doi:10.1038/s41467-019-14125-x · Cited by 31 · see citing works
The distinct roles of ROS in tumor immunity: from mechanisms to immunotherapeutic applications
Li, J., Huang, C., Tang, P., Wu, R., Wu, Q., & Zhang, C. (2026) · Journal of Hematology & Oncology · doi:10.1186/s13045-026-01780-z · Cited by 29 · see citing works
DAF-16 and SMK-1 Contribute to Innate Immunity During Adulthood in Caenorhabditis elegans
McHugh, D. R., Koumis, E., Jacob, P., Goldfarb, J. A., Schlaubitz-Garcia, M., Bennani, S., Regan, P., Patel, P., & Youngman, M. J. (2020) · G3 Genes Genomes Genetics · doi:10.1534/g3.120.401166 · Cited by 28 · see citing works
Kim, J. H., Talbot, H. K., Mishina, M., Zhu, Y., Chen, J., Cao, W., Reber, A. J., Griffin, M. R., Shay, D. K., Spencer, S., et al. (2016) · Vaccine · doi:10.1016/j.vaccine.2016.07.018 · Cited by 27 · see citing works
Mechanistic insights and biomarker discovery in immune cell aging and age-associated diseases
Upadhyay, P., Suhail, A., Khanal, P., & Kumar, S. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1637191 · Cited by 24 · see citing works
Innate immunity dysregulation in aging eye and therapeutic interventions
Das, S., Ahmad, Z., Suryawanshi, A. S., & Kumar, A. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101768 · Cited by 24 · see citing works
Naismith, E., & Pangrazzi, L. (2019) · Bioscience Reports · doi:10.1042/bsr20190371 · Cited by 24 · see citing works
Elderly-onset rheumatoid arthritis vs. polymyalgia rheumatica: Differences in pathogenesis
Wu, J., Yang, F., Ma, X., Lin, J., & Chen, W. (2023) · Frontiers in Medicine · doi:10.3389/fmed.2022.1083879 · Cited by 24 · see citing works
Immunosenescence in autoimmune diseases
Hu, H., Zhang, G., Chen, T., Liu, Y., Meng, L., Holmdahl, R., Dai, L., & Zhao, Y. C. (2025) · Autoimmunity Reviews · doi:10.1016/j.autrev.2025.103805 · Cited by 25 · see citing works
Steroid hormone regulation of immunometabolism and inflammation
Smith, L. C., Ramar, M., Riley, G., Mathias, C. B., & Lee, J.-Y. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1654034 · Cited by 25 · see citing works
Aldriwesh, M. G., Alotibi, R. S., Alqurainy, N., Alrabiah, S., Arafah, A. M., Alghoribi, M. F., & Ajina, R. (2025) · Gut Microbes · doi:10.1080/19490976.2025.2607076 · Cited by 20 · see citing works
Immune response to COVID-19 in older adults
Jergović, M., Coplen, C. P., Uhrlaub, J. L., & Nikolich‐Žugich, J. (2021) · The Journal of Heart and Lung Transplantation · doi:10.1016/j.healun.2021.04.017 · Cited by 20 · see citing works
Changaei, M., Tabrizi, Z. A., Karimi, M., Kashfi, S. A., Chahardeh, T. K., Hashemi, S. M., & Soudi, S. (2025) · Cell Communication and Signaling · doi:10.1186/s12964-025-02237-5 · Cited by 22 · see citing works
Fan, Y.-Y., Wu, H., & Xu, C. (2025) · Pharmaceutics · doi:10.3390/pharmaceutics17070886 · Cited by 19 · see citing works
Darling, R. J., Senapati, S., Christiansen, J. C., Liu, L., Ramer‐Tait, A. E., Narasimhan, B., & Wannemuehler, M. J. (2020) · International Journal of Nanomedicine · doi:10.2147/ijn.s261041 · Cited by 19 · see citing works
Conway, J., Certo, M., Lord, J. M., Mauro, C., & Duggal, N. A. (2021) · British Journal of Pharmacology · doi:10.1111/bph.15671 · Cited by 19 · see citing works
Senapati, S., Darling, R. J., Ross, K. A., Wannemuehler, M. J., Narasimhan, B., & Mallapragada, S. K. (2021) · Science Advances · doi:10.1126/sciadv.abj1691 · Cited by 19 · see citing works
Expression of Human Mutant Huntingtin Protein in Drosophila Hemocytes Impairs Immune Responses
Lin, Y.-H., Maaroufi, H. O., Ibrahim, E., Kučerová, L., & Žurovec, M. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02405 · Cited by 17 · see citing works
Understanding and improving vaccine efficacy in older adults
Hofer, S. J., Rapp, S., Klenerman, P., & Simon, A. K. (2025) · Nature Aging · doi:10.1038/s43587-025-00939-6 · Cited by 21 · see citing works
Moustaki, A., Crawford, J. C., Alli, S., Fan, Y., Boi, S. K., Zamora, A. E., McDonald, N., Wu, G., Nakitandwe, J., Newman, S., et al. (2022) · Science Immunology · doi:10.1126/sciimmunol.abf6136 · Cited by 17 · see citing works
Alterations in metabolic pathways: a bridge between aging and weaker innate immune response
Saleh, Z., Mirzazadeh, S., Mirzaei, F., Heidarnejad, K., Meri, S., & Kalantar, K. (2024) · Frontiers in Aging · doi:10.3389/fragi.2024.1358330 · Cited by 16 · see citing works
The Regulation of Cellular Senescence in Cancer
Zhang, X., Gao, Y., Zhang, S., Wang, Y., Du, Y., Hao, S., & Ni, T. (2025) · Biomolecules · doi:10.3390/biom15030448 · Cited by 16 · see citing works
Mito-xenophagic killing of bacteria is coordinated by a metabolic switch in dendritic cells
Radomski, N., Kägebein, D., Liebler–Tenorio, E., Karger, A., Rufer, E., Tews, B. A., Nagel, S., Einenkel, R., Müller, A., Rebbig, A., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-04142-5 · Cited by 16 · see citing works
- 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)
- ORCID
- Venue
- The Journal of Immunology
- Publisher
- Oxford University Press (OUP)
- Published
- 2015-09
- Volume
- 195
- Issue
- 6
- Pages
- 2624-2632
- ISSN
- 0022-1767 (ISSN-L)
- 1550-6606
- PMC
- PMC4561185
- 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
- bronze
- doi.org
- 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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review