The DOI matches its Crossref record; 69 of the 70 references it cites were found in a registry or an index.
Epigenetic programming of monocyte-to-macrophage differentiation and trained innate immunity
Open accessAbstract
Monocyte differentiation into macrophages represents a cornerstone process for host defense. Concomitantly, immunological imprinting of either tolerance or trained immunity determines the functional fate of macrophages and susceptibility to secondary infections. We characterized the transcriptomes and epigenomes in four primary cell types: monocytes and in vitro-differentiated naïve, tolerized, and trained macrophages. Inflammatory and metabolic pathways were modulated in macrophages, including decreased inflammasome activation, and we identified pathways functionally implicated in trained immunity. β-glucan training elicits an exclusive epigenetic signature, revealing a complex network of enhancers and promoters. Analysis of transcription factor motifs in deoxyribonuclease I hypersensitive sites at cell-type-specific epigenetic loci unveiled differentiation and treatment-specific repertoires. Altogether, we provide a resource to understand the epigenetic changes that underlie innate immunity in humans.
Overview
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
Verification
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“The same modifications of histone 3 were present in immune relevant gene locations in myeloid cells of humans and mice after induction of trained immunity [8,9,40].”
From Trained Immunity Provides Long-Term Protection against Bacterial Infections in Channel Catfish (2022) · cites this paper as [9]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Beta glucan exposure can induce these modifications in mammals, via the dectin-1 receptor [7,8,9].”
From Trained Immunity Provides Long-Term Protection against Bacterial Infections in Channel Catfish (2022) · cites this paper as [9]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Trained immunity in mice results from epigenetic reprogramming of monocytes and macrophages through acetylation or methylation of specific lysines in the histone-H3 [8,9].”
From Trained Immunity Provides Long-Term Protection against Bacterial Infections in Channel Catfish (2022) · cites this paper as [9]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“PCA of our human microglial and published monocyte and macrophage data 30 indicated that these three data sets segregated and that microglia were the most distinct ( Supplementary Figure 1a ).”
From Transcriptomic analysis of purified human cortical microglia reveals age-associated changes (2017) · cites this paper as [30]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Macrophage plasticity and polarization: in vivo veritas
Sica, A., & Mantovani, A. (2012) · Journal of Clinical Investigation · doi:10.1172/jci59643 · Cited by 6,335
Monocyte and macrophage heterogeneity
Gordon, S., & Taylor, P. R. (2005) · Nature Reviews Immunology · doi:10.1038/nri1733 · Cited by 5,190
Macrophage biology in development, homeostasis and disease
Wynn, T. A., Chawla, A., & Pollard, J. W. (2013) · Nature · doi:10.1038/nature12034 · Cited by 4,684
Development of Monocytes, Macrophages, and Dendritic Cells
Geissmann, F., Manz, M. G., Jung, S., Sieweke, M. H., Merad, M., & Ley, K. (2010) · Science · doi:10.1126/science.1178331 · Cited by 3,049
The accessible chromatin landscape of the human genome
Thurman, R. E., Rynes, E., Humbert, R., Vierstra, J., Maurano, M. T., Haugen, E., Sheffield, N. C., Stergachis, A. B., Wang, H., Vernot, B., et al. (2012) · Nature · doi:10.1038/nature11232 · Cited by 2,679
Regulation and Function of NF-κB Transcription Factors in the Immune System
Vallabhapurapu, S., & Karin, M. (2009) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132641 · Cited by 2,635
Histone modifications at human enhancers reflect global cell-type-specific gene expression
Heintzman, N. D., Hon, G. C., Hawkins, R. D., Kheradpour, P., Stark, A., Harp, L. F., Ye, Z., Lee, L. K., Stuart, R. K., Ching, C. W., et al. (2009) · Nature · doi:10.1038/nature07829 · Cited by 2,533
Martínez, F. O., Gordon, S., Locati, M., & Mantovani, A. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.10.7303 · Cited by 2,399
A unique chromatin signature uncovers early developmental enhancers in humans
Rada-Iglesias, A., Bajpai, R., Swigut, T., Brugmann, S. A., Flynn, R. A., & Wysocka, J. (2011) · Nature · doi:10.1038/nature09692 · Cited by 2,233
mTOR- and HIF-1α–mediated aerobic glycolysis as metabolic basis for trained immunity
Cheng, S.-C., Quintin, J., Cramer, R. A., Shepardson, K. M., Saeed, S., Kumar, V., Giamarellos-Bourboulis, E. J., Martens, J. H. A., Rao, N. A., Aghajanirefah, A., et al. (2014) · Science · doi:10.1126/science.1250684 · Cited by 2,224
Self-citation
Cited by
Sorted by citations
Items 301–400 of 1,003
Lecoeur, H., Prina, E., Rosazza, T., Kokou, K., N’Diaye, P., Aulner, N., Varet, H., Bussotti, G., Xing, Y., Milon, G., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.01.030 · Cited by 93
Jagannathan, P., Lutwama, F., Boyle, M. J., Nankya, F., Farrington, L. A., McIntyre, T. I., Bowen, K., Naluwu, K., Nalubega, M., Musinguzi, K., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-10624-3 · Cited by 84
miR-194-5p/BCLAF1 deregulation in AML tumorigenesis
Dell’Aversana, C., Giorgio, C., D'Amato, L., Lania, G., Matarese, F., Saeed, S., Costanzo, A. D., Petrizzi, V. B., Ingenito, C., Martens, J. H. A., et al. (2017) · Leukemia · doi:10.1038/leu.2017.64 · Cited by 84
Self-citationZiogas, A., & Netea, M. G. (2022) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2022.03.009 · Cited by 82
Self-citationImpact of aging on immunity in the context of COVID-19, HIV, and tuberculosis
Grifoni, A., Alonzi, T., Alter, G., Noonan, D. M., LANDAY, A. L., Albini, A., & Goletti, D. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1146704 · Cited by 90
Liang, J., Zhu, F., Cheng, K., Ma, N., Ma, X., Feng, Q., Xu, C., Gao, X., Wang, X., Shi, J., et al. (2023) · Advanced Materials · doi:10.1002/adma.202306158 · Cited by 84
Liu, Y., Reynolds, L. M., Ding, J., Hou, L., Lohman, K., Young, T., Cui, W., Huang, Z., Grenier, C., Wan, M., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-00517-4 · Cited by 83
Self-citationRemembering Pathogen Dose: Long-Term Adaptation in Innate Immunity
Bauer, M. W., Weis, S., Netea, M. G., & Wetzker, R. (2018) · Trends in Immunology · doi:10.1016/j.it.2018.04.001 · Cited by 83
Self-citationEpigenetics in diabetic nephropathy, immunity and metabolism
Keating, S. T., van Diepen, J. A., Riksen, N. P., & El-Osta, A. (2018) · Diabetologia · doi:10.1007/s00125-017-4490-1 · Cited by 82
Distinct mechanisms of the newborn innate immunity
Kumar, S. K. M., & Bhat, B. V. (2016) · Immunology Letters · doi:10.1016/j.imlet.2016.03.009 · Cited by 95
Bandyopadhaya, A., Tsurumi, A., Maura, D., Jeffrey, K. L., & Rahme, L. G. (2016) · Nature Microbiology · doi:10.1038/nmicrobiol.2016.174 · Cited by 82
Cross, D. L., Drury, R. E., Hill, J. W., & Pollard, A. J. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01363 · Cited by 83
Metabolic Reprogramming in Mitochondria of Myeloid Cells
Zuo, H., & Wan, Y. (2019) · Cells · doi:10.3390/cells9010005 · Cited by 83
Mossel, D. M., Moganti, K., Riabov, V., Weiß, C., Kopf, S., Cordero, J., Dobreva, G. D., Rots, M. G., Klüter, H., Harmsen, M. C., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01071 · Cited by 82
Tercan, H., Riksen, N. P., Joosten, L. A. B., Netea, M. G., & Bekkering, S. (2020) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.120.314212 · Cited by 97
Self-citationMcGarry, T., Hanlon, M. M., Marzaioli, V., Cunningham, C. C., Krishna, V., Murray, K., Hurson, C. J., Gallagher, P., Nagpal, S., Veale, D. J., et al. (2021) · Clinical & Translational Immunology · doi:10.1002/cti2.1237 · Cited by 89
Why don’t we have an effective tuberculosis vaccine yet?
Davenne, T., & McShane, H. (2016) · Expert Review of Vaccines · doi:10.1586/14760584.2016.1170599 · Cited by 79
The European Hematology Association Roadmap for European Hematology Research: a consensus document
Engert, A., Balduini, C., Brand, A., Coiffier, B., Cordonnier, C., Dohner, H., de Wit, T. D., Eichinger, S., Fibbe, W., Green, T., et al. (2016) · Haematologica · doi:10.3324/haematol.2015.136739 · Cited by 81
The Cell Biology of the Trichosporon-Host Interaction
Duarte‐Oliveira, C., Rodrigues, F. J. S., Gonçalves, S. M., Goldman, G. H., Carvalho, A., & Cunha, C. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00118 · Cited by 82
Altered metabolic pathways regulate synovial inflammation in rheumatoid arthritis
Fearon, U., Hanlon, M. M., Wade, S. M., & Fletcher, J. M. (2018) · Clinical & Experimental Immunology · doi:10.1111/cei.13228 · Cited by 84
Yoshida, K., Maekawa, T., Ly, N. H., Fujita, S.-I., Muratani, M., Ando, M., Katou, Y., Araki, H., Miura, F., Shirahige, K., et al. (2020) · Molecular Cell · doi:10.1016/j.molcel.2020.02.028 · Cited by 82
Barutta, F., Bellini, S., Durazzo, M., & Gruden, G. (2022) · Biomedicines · doi:10.3390/biomedicines10010178 · Cited by 88
Atherosclerosis in diabetes mellitus: novel mechanisms and mechanism-based therapeutic approaches
Khan, A. W., & Jandeleit-Dahm, K. A. M. (2025) · Nature Reviews Cardiology · doi:10.1038/s41569-024-01115-w · Cited by 93
Iwanowycz, S., Wang, J., Altomare, D., Hui, Y. Y., & Fan, D. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.702092 · Cited by 81
Chan, L. C., Rossetti, M., Miller, L. S., Filler, S. G., Johnson, C. W., Lee, H. K., Wang, H., Gjertson, D. W., Fowler, V. G., Reed, E. F., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1808353115 · Cited by 81
Smith, S. G., Kleinnijenhuis, J., Netea, M. G., & Dockrell, H. M. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00644 · Cited by 83
Self-citationTherapeutic Epigenetic Reprogramming of Trained Immunity in Myeloid Cells
Rodríguez, R. M. A., Suárez-Álvarez, B., & López‐Larrea, C. (2018) · Trends in Immunology · doi:10.1016/j.it.2018.11.006 · Cited by 76
Camilli, G., Bohm, M., Piffer, A. C., Lavenir, R., Williams, D. L., Neven, B., Grateau, G., Georgin‐Lavialle, S., & Quintin, J. (2020) · Journal of Clinical Investigation · doi:10.1172/jci134778 · Cited by 81
Self-citationGaziano, R., Sabbatini, S., & Monari, C. (2023) · Microorganisms · doi:10.3390/microorganisms11051211 · Cited by 84
Contact, Collaboration, and Conflict: Signal Integration of Syk-Coupled C-Type Lectin Receptors
Ostrop, J., & Lang, R. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1601665 · Cited by 85
Reprogramming of macrophages — new opportunities for therapeutic targeting
Schultze, J. L. (2015) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2015.09.007 · Cited by 79
Beyond receptors and signaling: epigenetic factors in the regulation of innate immunity
Mehta, S., & Jeffrey, K. L. (2015) · Immunology and Cell Biology · doi:10.1038/icb.2014.101 · Cited by 81
Chi, G. C., Liu, Y., MacDonald, J. W., Barr, R. G., Donohue, K. M., Hensley, M. D., Hou, L., McCall, C. E., Reynolds, L. M., Siscovick, D. S., et al. (2016) · Environmental Health · doi:10.1186/s12940-016-0202-4 · Cited by 79
Regeneration associated transcriptional signature of retinal microglia and macrophages
Mitchell, D. M., Sun, C. C., Hunter, S. S., New, D. D., & Stenkamp, D. L. (2019) · Scientific Reports · doi:10.1038/s41598-019-41298-8 · Cited by 80
LXR Activation Induces a Proinflammatory Trained Innate Immunity-Phenotype in Human Monocytes
Sohrabi, Y., Sonntag, G. V. H., Braun, L. C., Lagache, S. M. M., Liebmann, M., Klotz, L., Godfrey, R., Kahles, F., Waltenberger, J. L., & Findeisen, H. M. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00353 · Cited by 80
The Elusive Anti-Candida Vaccine: Lessons From the Past and Opportunities for the Future
Tso, G. H. W., Reales‐Calderón, J. A., & Pavelka, N. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00897 · Cited by 80
Innate immunity to malaria—The role of monocytes
Dobbs, K. R., Crabtree, J., & Dent, A. E. (2019) · Immunological Reviews · doi:10.1111/imr.12830 · Cited by 85
A century of BCG: Impact on tuberculosis control and beyond
Ahmed, A., Rakshit, S., Adiga, V., Dias, M., Dwarkanath, P., D′Souza, G., & Vyakarnam, A. (2021) · Immunological Reviews · doi:10.1111/imr.12968 · Cited by 74
Drummer, C., Saaoud, F., Jhala, N. C., Cueto, R., Sun, Y., Xu, K., Shao, Y., Lu, Y., Shen, H., Yang, L., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1113883 · Cited by 78
The mineralocorticoid receptor as a modulator of innate immunity and atherosclerosis
van der Heijden, C. D. C. C., Deinum, J., Joosten, L. A. B., Netea, M. G., & Riksen, N. P. (2018) · Cardiovascular Research · doi:10.1093/cvr/cvy092 · Cited by 79
Self-citationRecent advances in understanding neutrophils
Deniset, J., & Kubes, P. (2016) · F1000Research · doi:10.12688/f1000research.9691.1 · Cited by 77
Pan, Y., Li, J., Xia, X., Wang, J., Jiang, Q., Yang, J., Dou, H., Liang, H., Li, K., & Hou, Y. (2021) · Theranostics · doi:10.7150/thno.64874 · Cited by 78
Epigenetics and Proteomics Join Transcriptomics in the Quest for Tuberculosis Biomarkers
Esterhuyse, M. M., Weiner, J. M., Caron, É., Loxton, A. G., Iannaccone, M., Wagman, C., Saikali, P., Stanley, K., Wolski, W., Mollenkopf, H., et al. (2015) · mBio · doi:10.1128/mbio.01187-15 · Cited by 75
Guha, R., Mathioudaki, A., Doumbo, S., Doumtabé, D., Skinner, J., Arora, G., Siddiqui, S., Li, S., Kayentao, K., Ongoïba, A., et al. (2021) · PLoS Pathogens · doi:10.1371/journal.ppat.1009430 · Cited by 75
Russell, S. K., Harrison, J. K., Olson, B. S., Lee, H. J., O'Brien, V. P., Xing, X., Livny, J., Yu, L., Roberson, E. D. O., Bomjan, R., et al. (2023) · Nature Microbiology · doi:10.1038/s41564-023-01346-6 · Cited by 75
Farrington, L. A., Vance, H., Rek, J. C., Prahl, M. K., Jagannathan, P., Katureebe, A., Arinaitwe, E., Kamya, M. R., Dorsey, G., & Feeney, M. E. (2017) · Malaria Journal · doi:10.1186/s12936-017-2148-6 · Cited by 76
Zimmermann, M. T., Oberg, A. L., Grill, D. E., Ovsyannikova, I. G., Haralambieva, I. H., Kennedy, R. B., & Poland, G. A. (2016) · PLoS ONE · doi:10.1371/journal.pone.0152034 · Cited by 71
Innate immune memory in mammals
Hamon, M. A., & Quintin, J. (2016) · Seminars in Immunology · doi:10.1016/j.smim.2016.05.003 · Cited by 81
Self-citationImmunometabolism orchestrates training of innate immunity in atherosclerosis
van Tuijl, J., Joosten, L. A. B., Netea, M. G., Bekkering, S., & Riksen, N. P. (2019) · Cardiovascular Research · doi:10.1093/cvr/cvz107 · Cited by 77
Self-citationChronic HIV infection induces transcriptional and functional reprogramming of innate immune cells
van der Heijden, W. A., de Wijer, L. V., Keramati, F., Trypsteen, W., Rutsaert, S., ter Horst, R., Jaeger, M., Koenen, H. J. P. M., Stunnenberg, H. G., Joosten, I., et al. (2021) · JCI Insight · doi:10.1172/jci.insight.145928 · Cited by 73
Self-citationThe BCG Vaccine for COVID-19: First Verdict and Future Directions
González-Pérez, M., Sánchez-Tarjuelo, R., Shor, B., Nistal‐Villán, E., & Ochando, J. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.632478 · Cited by 78
Verma, M., Michalec, L., Sripada, A., McKay, J. T., Sirohi, K., Verma, D., Sheth, D., Martin, R. J., Dyjack, N. T., Seibold, M. A., et al. (2021) · The Journal of Experimental Medicine · doi:10.1084/jem.20201354 · Cited by 76
Development and Function of Arterial and Cardiac Macrophages
Świrski, F. K., Robbins, C. S., & Nahrendorf, M. (2015) · Trends in Immunology · doi:10.1016/j.it.2015.11.004 · Cited by 78
Raulien, N., Friedrich, K., Strobel, S., Rubner, S., Baumann, S., von Bergen�, M., Körner, A., Krueger, M. C., Rossol, M., & Wagner, U. G. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00609 · Cited by 76
Vaccari, M., Fourati, S., Gordon, S. N., Brown, D. R., Bissa, M., Schifanella, L., de Castro, I. S., Doster, M. N., Galli, V., Omsland, M., et al. (2018) · Nature Medicine · doi:10.1038/s41591-018-0025-7 · Cited by 76
Carballo, C., Chronopoulou, E. G., Letsiou, S., Maya, C., Labrou, N. E., Infante, C., Power, D. M., & Manchado, M. (2018) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2018.07.052 · Cited by 78
Innate Immune Modulation by GM-CSF and IL-3 in Health and Disease
Borriello, F., Galdiero, M. R., Varricchi, G., Loffredo, S., Spadaro, G., & Marone, G. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20040834 · Cited by 77
HDAC3 Mediates the Inflammatory Response and LPS Tolerance in Human Monocytes and Macrophages
Ghiboub, M., Zhao, J., Yim, A. Y. F. L., Schilderink, R., Verseijden, C., van Hamersveld, P. H. P., Duarte, J. M., Hakvoort, T. B. M., Admiraal, I., Harker, N., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.550769 · Cited by 74
Linking vaccine adjuvant mechanisms of action to function
Ben‐Akiva, E., Chapman, A. P., Mao, T., & Irvine, D. J. (2025) · Science Immunology · doi:10.1126/sciimmunol.ado5937 · Cited by 83
Sepsis Induces a Long-Lasting State of Trained Immunity in Bone Marrow Monocytes
Bomans, K., Schenz, J., Sztwiertnia, I., Schaack, D., Weigand, M. A., & Uhle, F. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02685 · Cited by 73
Wang, A., Pope, S. D., Weinstein, J. S., Yu, S., Zhang, C., Booth, C. J., & Medzhitov, R. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1820704116 · Cited by 67
Janbon, G., Quintin, J., Lanternier, F., & d’Enfert, C. (2019) · Genes and Immunity · doi:10.1038/s41435-019-0071-2 · Cited by 74
Self-citationYang, W., Tran, N. T., Zhu, C., Yao, D., Aweya, J. J., Gong, Y., Ma, H., Zhang, Y., Li, G., & Li, S. (2020) · Aquaculture · doi:10.1016/j.aquaculture.2020.735831 · Cited by 72
IGF2R-initiated proton rechanneling dictates an anti-inflammatory property in macrophages
Wang, X., Lin, L., Lan, B., Wang, Y., Du, L., Chen, X., Li, Q., Liu, K., Hu, M., Xue, Y., et al. (2020) · Science Advances · doi:10.1126/sciadv.abb7389 · Cited by 72
DAMPs and Innate Immune Training
Jentho, E., & Weis, S. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.699563 · Cited by 73
Ferreira, A. V., Kostidis, S., Groh, L. A., Koeken, V. A. C. M., Bruno, M., Baydemir, İ., Kılıç, G., Bulut, O. P., Andriopoulou, T., Spanou, V. M., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112658 · Cited by 77
Self-citationMulti-omics approaches to decipher the interactions of nanoparticles and biological systems
Wang, Y., Xiao, Z., Wang, Z., Lee, D., Ma, Y., Wilhelm, S., Wang, H., Kim, B. Y. S., & Jiang, W. (2024) · Nature Reviews Bioengineering · doi:10.1038/s44222-024-00264-4 · Cited by 82
Differential peak calling of ChIP-seq signals with replicates with THOR
Allhoff, M., Seré, K., Pires, J. F., Zenke, M., & Costa, I. G. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw680 · Cited by 75
Hammer, Q., & Romagnani, C. (2016) · Advances in immunology · doi:10.1016/bs.ai.2016.10.001 · Cited by 72
Helminths in the gastrointestinal tract as modulators of immunity and pathology
Varyani, F., Fleming, J. O., & Maizels, R. M. (2017) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00024.2017 · Cited by 81
Postnatal Age Is a Critical Determinant of the Neonatal Host Response to Sepsis
Wynn, J. L., Guthrie, S. O., Wong, H. R., Lahni, P. M., Ungaro, R. F., López, M. C., Baker, H. V., & Moldawer, L. L. (2015) · Molecular Medicine · doi:10.2119/molmed.2015.00064 · Cited by 72
The lncRNA Connection Between Cellular Metabolism and Epigenetics in Trained Immunity
Fok, E. T., Davignon, L., Fanucchi, S., & Mhlanga, M. M. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2018.03184 · Cited by 76
Candida innate immunity at the mucosa
Richardson, J. P., Moyes, D. L., Ho, J., & Naglik, J. R. (2018) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2018.02.026 · Cited by 69
The “ART” of Epigenetics in Melanoma: From histone “Alterations, to Resistance and Therapies”
Strub, T., Ballotti, R., & Bertolotto, C. (2020) · Theranostics · doi:10.7150/thno.36218 · Cited by 73
PAMPs of the Fungal Cell Wall and Mammalian PRRs
Hatinguais, R., Willment, J. A., & Brown, G. D. (2020) · Current topics in microbiology and immunology · doi:10.1007/82_2020_201 · Cited by 80
Cotechini, T., Atallah, A., & Grossman, A. (2021) · Cells · doi:10.3390/cells10040960 · Cited by 74
IL-1 family cytokines as drivers and inhibitors of trained immunity
Teufel, L. U., Arts, R. J. W., Netea, M. G., Dinarello, C. A., & Joosten, L. A. B. (2021) · Cytokine · doi:10.1016/j.cyto.2021.155773 · Cited by 73
Self-citationEpigenetic pathways in macrophages emerge as novel targets in atherosclerosis
Neele, A. E., den Bossche, J. V., Hoeksema, M. A., & de Winther, M. P. J. (2015) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2015.03.101 · Cited by 72
Macrophage reprogramming for therapy
Bart, V. M. T., Pickering, R. J., Taylor, P. R., & Ipseiz, N. (2020) · Immunology · doi:10.1111/imm.13300 · Cited by 73
TLR4 is a regulator of trained immunity in a murine model of Duchenne muscular dystrophy
Bhattarai, S., Li, Q., Ding, J., Liang, F., Gusev, E., Lapohos, O., Fonseca, G. J., Kaufmann, E., Divangahi, M., & Petrof, B. J. (2022) · Nature Communications · doi:10.1038/s41467-022-28531-1 · Cited by 72
Trained immunity: A “new” weapon in the fight against infectious diseases
Dagenais, A., Villalba-Guerrero, C., & Olivier, M. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1147476 · Cited by 81
Iliev, I. D., Brown, G. D., Bächer, P., Gaffen, S. L., Heitman, J., Klein, B. S., & Lionakis, M. S. (2024) · Cell · doi:10.1016/j.cell.2024.08.016 · Cited by 71
Infection-adapted emergency hematopoiesis promotes visceral leishmaniasis
Abidin, B. M., Hammami, A., Stäger, S., & Heinonen, K. M. (2017) · PLoS Pathogens · doi:10.1371/journal.ppat.1006422 · Cited by 67
Trained immunity as a novel therapeutic strategy
Mourits, V. P., Wijkmans, J. C., Joosten, L. A. B., & Netea, M. G. (2018) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2018.04.007 · Cited by 69
Self-citationWang, Z., Long, H., Chang, C., Zhao, M., & Lu, Q. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-018-2864-2 · Cited by 69
Current and Future Nutritional Strategies to Modulate Inflammatory Dynamics in Metabolic Disorders
van den Brink, W., van Bilsen, J. H. M., Salic, K., Hoevenaars, F. P. M., Verschuren, L., Kleemann, R., Bouwman, J., Ronnett, G. V., van Ommen, B., & Wopereis, S. (2019) · Frontiers in Nutrition · doi:10.3389/fnut.2019.00129 · Cited by 74
Gu, Y., Lawrence, T., Mohamed, R., Liang, Y., & Yahaya, B. H. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.923235 · Cited by 73
Fonseca, S., Carvalho, A. L., Miquel-Clopés, A., Jones, E. J., Juodeikis, R., Stentz, R., & Carding, S. R. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.1050271 · Cited by 71
Potent induction of trained immunity by Saccharomyces cerevisiae β-glucans
Vuscan, P., Kischkel, B., Hatzioannou, A., Markaki, E., Sarlea, A., Tintoré, M., Cuñé, J., Verginis, P., de Lecea, C., Chavakis, T., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1323333 · Cited by 74
Self-citationSynergistic interactions between NOD receptors and TLRs: Mechanisms and clinical implications
Pashenkov, M. V., Евгеньевна, М. Н., Budikhina, A. S., & Pinegin, B. V. (2018) · Journal of Leukocyte Biology · doi:10.1002/jlb.2ru0718-290r · Cited by 73
Quinn, S. M., Cunningham, K. T., Raverdeau, M., Walsh, R. J., Curham, L. M., Malara, A., & Mills, K. H. G. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01109 · Cited by 70
Endogenous Retroviruses Transcriptional Modulation After Severe Infection, Trauma and Burn
Tabone, O., Mommert, M., Jourdan, C., Cerrato, E., Legrand, M. M., Lepape, A., Allaouchiche, B., Rimmelé, T., Pachot, A., Monneret, G., et al. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2018.03091 · Cited by 70
Wang, Y., Wang, K., Masso-Silva, J. A., Rivera, A., & Xue, C. (2019) · mBio · doi:10.1128/mbio.02145-19 · Cited by 68
Angelidou, A., Diray‐Arce, J., Conti, M. G., Smolen, K. K., van Haren, S. D., Dowling, D. J., Husson, R. N., & Levy, O. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.00332 · Cited by 70
Diabetes propels the risk for cardiovascular disease: sweet monocytes becoming aggressive?
van Diepen, J. A., Thiem, K., Stienstra, R., Riksen, N. P., Tack, C. J., & Netea, M. G. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2316-9 · Cited by 68
Self-citationMemory γδ T Cells–Newly Appreciated Protagonists in Infection and Immunity
Lalor, S. J., & McLoughlin, R. M. (2016) · Trends in Immunology · doi:10.1016/j.it.2016.07.006 · Cited by 70
Liu, N. Q., ter Huurne, M., Nguyen, L. N. M., Peng, T., Wang, S.-Y., Studd, J. B., Joshi, O., Ongen, H., Bramsen, J. B., Yan, J., et al. (2017) · Nature Communications · doi:10.1038/ncomms14418 · Cited by 68
Self-citationMurine Monocytes: Origins, Subsets, Fates, and Functions
Mildner, A., Marinković, G., & Jung, S. (2016) · Microbiology Spectrum · doi:10.1128/microbiolspec.mchd-0033-2016 · Cited by 68
Madej, M. P., Töpfer, E., Boraschi, D., & Italiani, P. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00335 · Cited by 65
Innate Immunity to Mucosal Candida Infections
Verma, A. H., Gaffen, S. L., & Swidergall, M. (2017) · Journal of Fungi · doi:10.3390/jof3040060 · Cited by 67
Metadata
- Authors
- Saeed, S., Quintin, J., Kerstens, H. H. D., Rao, N. A., Aghajanirefah, A., Matarese, F., Cheng, S.-C., Ratter, J., Berentsen, K., van der Ent, M. A., Sharifi, N., Janssen-Megens, E. M., Ter Huurne, M., Mandoli, A., van Schaik, T., Ng, A., Burden, F., Downes, K., Frontini, M., Kumar, V., Giamarellos-Bourboulis, E. J., Ouwehand, W. H., van der Meer, J. W. M., Joosten, L. A. B., Wijmenga, C., Martens, J. H. A., Xavier, R. J., Logie, C., Netea, M. G., & Stunnenberg, H. G.
- Affiliations
- Radboud University Nijmegen (NL)
- Radboud University Medical Center (NL)
- Department of Molecular Biology, Faculties of Science and Medicine, Radboud Institute for Molecular Life Sciences, Radboud University, 6500 HB Nijmegen, Netherlands.
- Broad Institute (US)
- National Health Service (GB)
- University Medical Center Groningen (NL)
- Fourth Department of Internal Medicine, University of Athens, Medical School, 1 Rimini Street, 12462 Athens, Greece.
- Department of Internal Medicine, Radboud University Medical Center, 6525 GA Nijmegen, Netherlands.
- Corresponding author
- Saeed, Sadia
- Quintin, Jessica
- Kerstens, Hindrik H. D.
- Rao, Nagesha A.
- Aghajanirefah, Ali
- Logie, Colin
- Netea, Mihai G.
- Stunnenberg, Hendrik G.
- ORCID
- Venue
- Science
- Published
- 2014-09-26
- Volume
- 345
- Issue
- 6204
- Pages
- 1251086-1251086
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC4242194
- OpenAlex
- W2140876277
- Cited by
- 1,761
- References
- 70
- Citations by year
- 2026: 197 · 2025: 162 · 2024: 143 · 2023: 150 · 2022: 174 · 2021: 184 · 2020: 168 · 2019: 134 · 2018: 129 · 2017: 114 · 2016: 120 · 2015: 76 · 2014: 9
- FWCI
- 48.54
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- HAL (submittedVersion)
- University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion)
- Radboud Repository (Radboud University) (submittedVersion)
- Funders
- National Institute for Health and Care Research (NF-SI-0510-10214, RP-PG-0310-1002, NF-SI-0513-10151)
- British Heart Foundation (RG/09/012/28096)
- National Institute of Diabetes and Digestive and Kidney Diseases (P30DK043351)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune responses and vaccinations
- Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Keywords
- monocyte-to-macrophage differentiation, trained immunity, immunological imprinting, epigenetic programming, macrophage transcriptome, inflammasome activation, transcription factor binding motifs, innate immunity
- MeSH terms
- Animals, Binding Sites, Cell Differentiation, Deoxyribonuclease I, Humans, Immunity, Innate, Immunologic Memory, Macrophages, Monocytes, Transcription Factors, Genomic Imprinting, Epigenesis, Genetic, beta-Glucans, Mice, Inflammasomes
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