The DOI matches its Crossref record; 35 of the 35 references it cites were found in a registry or an index.
Bacille Calmette-Guérin induces NOD2-dependent nonspecific protection from reinfection via epigenetic reprogramming of monocytes
Open accessAbstract
Adaptive features of innate immunity, recently described as “trained immunity,” have been documented in plants, invertebrate animals, and mice, but not yet in humans. Here we show that bacille Calmette-Guérin (BCG) vaccination in healthy volunteers led not only to a four- to sevenfold increase in the production of IFN-γ, but also to a twofold enhanced release of monocyte-derived cytokines, such as TNF and IL-1β, in response to unrelated bacterial and fungal pathogens. The enhanced function of circulating monocytes persisted for at least 3 mo after vaccination and was accompanied by increased expression of activation markers such as CD11b and Toll-like receptor 4. These training effects were induced through the NOD2 receptor and mediated by increased histone 3 lysine 4 trimethylation. In experimental studies, BCG vaccination induced T- and B-lymphocyte–independent protection of severe combined immunodeficiency SCID mice from disseminated candidiasis (100% survival in BCG-vaccinated mice vs. 30% in control mice). In conclusion, BCG induces trained immunity and nonspecific protection from infections through epigenetic reprogramming of innate immune cells.
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?
In the citing paper
“our findings corroborate a wealth of emerging evidence that NOD2 stimulation by MDP and its analogs can alter host immunity through multiple pathways including the direct activation of macrophages for tumor cell clearance (39), epigenetic reprogramming of monocytes (40, 41), generation of conventional type 1 dendritic cells (42), and priming of dendritic cells for cross-presentation to CD8+ T cell”
From Enterococcus peptidoglycan remodeling promotes checkpoint inhibitor cancer immunotherapy (2021) · cites this paper as [40]
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 interaction with lymphocyte subsets: cancer as a paradigm
Biswas, S. K., & Mantovani, A. (2010) · Nature Immunology · doi:10.1038/ni.1937 · Cited by 3,840
Durrant, W. E., & Dong, X. (2004) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.42.040803.140421 · Cited by 3,184
Trained Immunity: A Memory for Innate Host Defense
Netea, M. G., Quintin, J., & van der Meer, J. W. M. (2011) · Cell Host & Microbe · doi:10.1016/j.chom.2011.04.006 · Cited by 1,760
Self-citationAdaptive Immune Features of Natural Killer Cells
Sun, J. C., Beilke, J., & Lanier, L. (2009) · Nature · doi:10.1038/nature07665 · Cited by 1,647
Variation in protection by BCG: implications of and for heterologous immunity
Fine, P. (1995) · The Lancet · doi:10.1016/s0140-6736(95)92348-9 · Cited by 1,385
Sylvester, R. J., van der Meijden, A. P. M., & Lamm, D. L. (2002) · The Journal of Urology · doi:10.1016/s0022-5347(05)64273-5 · Cited by 1,319
Trunz, B. B., Fine, P., & Dye, C. (2006) · The Lancet · doi:10.1016/s0140-6736(06)68507-3 · Cited by 1,114
T cell– and B cell–independent adaptive immunity mediated by natural killer cells
O’Leary, J. G., Goodarzi, M., Drayton, D. L., & von Andrian, U. H. (2006) · Nature Immunology · doi:10.1038/ni1332 · Cited by 920
REGULATION OF TH2 DIFFERENTIATION AND Il4 LOCUS ACCESSIBILITY
Ansel, K. M., Djuretic, I. M., Tanasă, B., & Rao, A. (2006) · Annual Review of Immunology · doi:10.1146/annurev.immunol.23.021704.115821 · Cited by 652
Aaby, P., Roth, A., Ravn, H., Napirna, B. M., Rodrigues, A., Lisse, I. M., Stensballe, L. G., Diness, B. R., Lausch, K. R., Lund, N., et al. (2011) · The Journal of Infectious Diseases · doi:10.1093/infdis/jir240 · Cited by 581
Cited by
Sorted by citations
Trained immunity: A program of innate immune memory in health and– disease
Netea, M. G., Joosten, L. A. B., Latz, E., Mills, K. H. G., Natoli, G., Stunnenberg, H. G., O’Neill, L. A. J., & Xavier, R. J. (2016) · Science · doi:10.1126/science.aaf1098 · Cited by 2,768
Self-citationDefining trained immunity and its role in health and disease
Netea, M. G., Domínguez-Andrés, J., Barreiro, L. B., Chavakis, T., Divangahi, M., Fuchs, E., Joosten, L. A. B., van der Meer, J. W. M., Mhlanga, M. M., Mulder, W. J. M., et al. (2020) · Nature Reviews Immunology · doi:10.1038/s41577-020-0285-6 · Cited by 2,690
Self-citationToll-like Receptors and the Control of Immunity
Fitzgerald, K. A., & Kagan, J. C. (2020) · Cell · doi:10.1016/j.cell.2020.02.041 · Cited by 2,168
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-citationMicroglial M1/M2 polarization and metabolic states
Orihuela, R., McPherson, C. A., & Harry, G. J. (2016) · British Journal of Pharmacology · doi:10.1111/bph.13139 · Cited by 2,070
Local and systemic mechanisms linking periodontal disease and inflammatory comorbidities
Hajishengallis, G., & Chavakis, T. (2021) · Nature Reviews Immunology · doi:10.1038/s41577-020-00488-6 · Cited by 1,871
Epigenetic programming of monocyte-to-macrophage differentiation and trained innate immunity
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., et al. (2014) · Science · doi:10.1126/science.1251086 · Cited by 1,761
Self-citationImmunosenescence and Inflamm-Aging As Two Sides of the Same Coin: Friends or Foes?
Fulop, T., Larbi, A., Dupuis, G., Le Page, A., Frost, E. H., Cohen, A. A., Witkowski, J. M., & Franceschi, C. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01960 · Cited by 1,364
Emerging concepts in the science of vaccine adjuvants
Pulendran, B., Arunachalam, P. S., & O’Hagan, D. T. (2021) · Nature Reviews Drug Discovery · doi:10.1038/s41573-021-00163-y · Cited by 1,446
BCG Educates Hematopoietic Stem Cells to Generate Protective Innate Immunity against Tuberculosis
Kaufmann, E., Sanz, J., Dunn, J. L., Khan, N., Mendonça, L. E., Pacis, A., Tzelepis, F., Pernet, E., Dumaine, A., Grenier, J.-C., et al. (2018) · Cell · doi:10.1016/j.cell.2017.12.031 · Cited by 1,191
Arts, R. J. W., Moorlag, S. J. C. F. M., Novakovic, B., Li, Y., Wang, S.-Y., Oosting, M., Kumar, V., Xavier, R. J., Wijmenga, C., Joosten, L. A. B., et al. (2018) · Cell Host & Microbe · doi:10.1016/j.chom.2017.12.010 · Cited by 1,217
Self-citationConrath, U., Beckers, G. J. M., Langenbach, C. J. G., & Jaskiewicz, M. R. (2015) · Annual Review of Phytopathology · doi:10.1146/annurev-phyto-080614-120132 · Cited by 1,117
Innate immune memory in the brain shapes neurological disease hallmarks
Wendeln, A.-C., Degenhardt, K., Kaurani, L., Gertig, M., Ulas, T., Jain, G., Wagner, J., Häsler, L. M., Wild, K., Skodras, A., et al. (2018) · Nature · doi:10.1038/s41586-018-0023-4 · Cited by 956
The contribution of vaccination to global health: past, present and future
Greenwood, B. M. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0433 · Cited by 1,050
Arts, R. J. W., Novakovic, B., ter Horst, R., Carvalho, A., Bekkering, S., Lachmandas, E., Rodrigues, F., Silvestre, R., Cheng, S.-C., Wang, S.-Y., et al. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.10.008 · Cited by 930
Self-citationEnhancing cancer immunotherapy with nanomedicine
Irvine, D. J., & Dane, E. L. (2020) · Nature reviews. Immunology · doi:10.1038/s41577-019-0269-6 · Cited by 908
NOD1 and NOD2: Signaling, Host Defense, and Inflammatory Disease
Caruso, R., Warner, N., Inohara, N., & Núñez, G. (2014) · Immunity · doi:10.1016/j.immuni.2014.12.010 · Cited by 830
Metabolic Induction of Trained Immunity through the Mevalonate Pathway
Bekkering, S., Arts, R. J. W., Novakovic, B., Kourtzelis, I., van der Heijden, C. D. C. C., Li, Y., Popa, C. D., ter Horst, R., van Tuijl, J., Netea-Maier, R. T., et al. (2018) · Cell · doi:10.1016/j.cell.2017.11.025 · Cited by 815
Self-citationCOVID-19 and the human innate immune system
Schultze, J. L., & Aschenbrenner, A. C. (2021) · Cell · doi:10.1016/j.cell.2021.02.029 · Cited by 714
“…important to see whether boosting the potential of proinflammatory cytokine production (IL-1, IL-6, and TNF) by the induction of trained immunity (Kleinnijenhuis et al., 2012) will exaggerate the observed hyperinflammatory cytokine responses in severe COVID-19, or whether trained immunity would…”
BackgroundBekkering, S., Quintin, J., Joosten, L. A. B., van der Meer, J. W. M., Netea, M. G., & Riksen, N. P. (2014) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.114.303887 · Cited by 735
Self-citationβ-Glucan Reverses the Epigenetic State of LPS-Induced Immunological Tolerance
Novakovic, B., Habibi, E., Wang, S.-Y., Arts, R. J. W., Davar, R., Megchelenbrink, W., Kim, B., Kuznetsova, T., Kox, M., Zwaag, J., et al. (2016) · Cell · doi:10.1016/j.cell.2016.09.034 · Cited by 712
Self-citationImmunometabolic Pathways in BCG-Induced Trained Immunity
Arts, R. J. W., Carvalho, A., Rocca, C. L., Palma, C., Rodrigues, F. J. S., Silvestre, R., Kleinnijenhuis, J., Lachmandas, E., Gonçalves, L. G., Belinha, A., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.11.011 · Cited by 690
Self-citationNOD proteins: regulators of inflammation in health and disease
Philpott, D. J., Sorbara, M. T., Robertson, S. J., Croitoru, K., & Girardin, S. E. (2014) · Nature Reviews Immunology · doi:10.1038/nri3565 · Cited by 668
Innate Immune Training of Granulopoiesis Promotes Anti-tumor Activity
Kalafati, L., Kourtzelis, I., Schulte-Schrepping, J., Li, X., Hatzioannou, A., Grinenko, T., Hagag, E., Sinha, A., Has, C., Dietz, S., et al. (2020) · Cell · doi:10.1016/j.cell.2020.09.058 · Cited by 648
Self-citationKleinnijenhuis, J., Quintin, J., Preijers, F. W. M. B., Benn, C. S., Joosten, L. A. B., Jacobs, C. W. M., van Loenhout, J., Xavier, R. J., Aaby, P., van der Meer, J. W. M., et al. (2013) · Journal of Innate Immunity · doi:10.1159/000355628 · Cited by 625
Self-citationInnate and Adaptive Immune Memory: an Evolutionary Continuum in the Host’s Response to Pathogens
Netea, M. G., Schlitzer, A., Placek, K., Joosten, L. A. B., & Schultze, J. L. (2019) · Cell Host & Microbe · doi:10.1016/j.chom.2018.12.006 · Cited by 644
Self-citationA small jab – a big effect: nonspecific immunomodulation by vaccines
Benn, C. S., Netea, M. G., Selin, L. K., & Aaby, P. (2013) · Trends in Immunology · doi:10.1016/j.it.2013.04.004 · Cited by 535
Self-citationBCG Vaccination in Humans Elicits Trained Immunity via the Hematopoietic Progenitor Compartment
Cirovic, B., de Bree, L. C. J., Groh, L., Blok, B. A., Chan, J., van der Velden, W. J. F. M., Bremmers, M. E. J., van Crevel, R., Händler, K., Picelli, S., et al. (2020) · Cell Host & Microbe · doi:10.1016/j.chom.2020.05.014 · Cited by 510
Self-citationNon-specific effects of BCG vaccine on viral infections
Moorlag, S. J. C. F. M., Arts, R. J. W., van Crevel, R., & Netea, M. G. (2019) · Clinical Microbiology and Infection · doi:10.1016/j.cmi.2019.04.020 · Cited by 479
Self-citationBCG-induced trained immunity: can it offer protection against COVID-19?
O'Neill, L. A. J., & Netea, M. G. (2020) · Nature reviews. Immunology · doi:10.1038/s41577-020-0337-y · Cited by 500
Self-citationBCG-induced trained immunity in NK cells: Role for non-specific protection to infection
Kleinnijenhuis, J., Quintin, J., Preijers, F. W. M. B., Joosten, L. A. B., Jacobs, C. W. M., Xavier, R. J., van der Meer, J. W. M., van Crevel, R., & Netea, M. G. (2014) · Clinical Immunology · doi:10.1016/j.clim.2014.10.005 · Cited by 490
Self-citationTrained Immunity: a Tool for Reducing Susceptibility to and the Severity of SARS-CoV-2 Infection
Netea, M. G., Giamarellos‐Bourboulis, E. J., Domínguez‐Andrés, J., Curtis, N. C., van Crevel, R., van de Veerdonk, F. L., & Bonten, M. J. M. (2020) · Cell · doi:10.1016/j.cell.2020.04.042 · Cited by 467
Self-citationImmunology of aging: the birth of inflammaging
Fulop, T., Larbi, A., Pawelec, G., Khalil, A., Cohen, A. A., Hirokawa, K., Witkowski, J. M., & Franceschi, C. (2021) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-021-08899-6 · Cited by 464
Trained immunity — basic concepts and contributions to immunopathology
Ochando, J., Mulder, W. J. M., Madsen, J. C., Netea, M. G., & Duivenvoorden, R. (2022) · Nature Reviews Nephrology · doi:10.1038/s41581-022-00633-5 · Cited by 504
Self-citationTherapeutic targeting of trained immunity
Mulder, W. J. M., Ochando, J., Joosten, L. A. B., Fayad, Z. A., & Netea, M. G. (2019) · Nature Reviews Drug Discovery · doi:10.1038/s41573-019-0025-4 · Cited by 456
Self-citationThe Intersection of Epigenetics and Metabolism in Trained Immunity
Fanucchi, S., Domínguez‐Andrés, J., Joosten, L. A. B., Netea, M. G., & Mhlanga, M. M. (2020) · Immunity · doi:10.1016/j.immuni.2020.10.011 · Cited by 458
Self-citationLong-term measles-induced immunomodulation increases overall childhood infectious disease mortality
Mina, M. J., Metcalf, C. J. E., de Swart, R. L., Osterhaus, A. D. M. E., & Grenfell, B. T. (2015) · Science · doi:10.1126/science.aaa3662 · Cited by 421
Sex Differences in Pediatric Infectious Diseases
Muenchhoff, M., & Goulder, P. (2014) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiu232 · Cited by 433
Activate: Randomized Clinical Trial of BCG Vaccination against Infection in the Elderly
Giamarellos‐Bourboulis, E. J., Τσιλικά, Μ., Moorlag, S. J. C. F. M., Antonakos, N., Kotsaki, A., Domínguez‐Andrés, J., Kyriazopoulou, E., Gkavogianni, T., Adami, M., Damoraki, G., et al. (2020) · Cell · doi:10.1016/j.cell.2020.08.051 · Cited by 407
Self-citationMacrophage Activation and Polarization as an Adaptive Component of Innate Immunity
Locati, M., Mantovani, A., & Sica, A. (2013) · Advances in immunology · doi:10.1016/b978-0-12-417028-5.00006-5 · Cited by 418
Enterococcus peptidoglycan remodeling promotes checkpoint inhibitor cancer immunotherapy
Griffin, M. E., Espinosa, J., Becker, J. L., Luo, J.-D., Carroll, T. S., Jha, J. K., Fanger, G. R., & Hang, H. C. (2021) · Science · doi:10.1126/science.abc9113 · Cited by 366
Ontogeny of early life immunity
Dowling, D. J., & Levy, O. (2014) · Trends in Immunology · doi:10.1016/j.it.2014.04.007 · Cited by 376
Ifrim, D. C., Quintin, J., Joosten, L. A. B., Jacobs, C. W. M., Jansen, T., Jacobs, L., Gow, N. A. R., Williams, D. L., van der Meer, J. W. M., & Netea, M. G. (2014) · Clinical and Vaccine Immunology · doi:10.1128/cvi.00688-13 · Cited by 373
Self-citationThe 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 368
In Vitro Experimental Model of Trained Innate Immunity in Human Primary Monocytes
Bekkering, S., Blok, B. A., Joosten, L. A. B., Riksen, N. P., van Crevel, R., & Netea, M. G. (2016) · Clinical and Vaccine Immunology · doi:10.1128/cvi.00349-16 · Cited by 364
Self-citationTrained Immunity: Reprogramming Innate Immunity in Health and Disease
Bekkering, S., Domínguez‐Andrés, J., Joosten, L. A. B., Riksen, N. P., & Netea, M. G. (2021) · Annual Review of Immunology · doi:10.1146/annurev-immunol-102119-073855 · Cited by 360
Self-citationMoorlag, S. J. C. F. M., Khan, N., Novakovic, B., Kaufmann, E., Jansen, T., van Crevel, R., Divangahi, M., & Netea, M. G. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107634 · Cited by 350
Self-citationNew insights into the evasion of host innate immunity by Mycobacterium tuberculosis
Chai, Q., Wang, L., Liu, C. H., & Ge, B. (2020) · Cellular and Molecular Immunology · doi:10.1038/s41423-020-0502-z · Cited by 347
BCG Vaccination Induces Long-Term Functional Reprogramming of Human Neutrophils
Moorlag, S. J. C. F. M., Rodriguez-Rosales, Y. A., Gillard, J., Fanucchi, S., Theunissen, K., Novakovic, B., de Bont, C. M., Negishi, Y., Fok, E. T., Kalafati, L., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108387 · Cited by 345
Self-citationBCG-Induced Cross-Protection and Development of Trained Immunity: Implication for Vaccine Design
Covián, C., Fernández‐Fierro, A., Retamal-Díaz, A. R., Díaz, F. E., Vasquez, A. E., Lay, M. K., Riedel, C. A., González, P. A., Bueno, S. M., & Kalergis, A. M. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02806 · Cited by 342
Pattern recognition receptors: function, regulation and therapeutic potential
Chen, R., Zou, J., Chen, J., Zhong, X. Y., Kang, R., & Tang, D. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02264-1 · Cited by 392
Martínez-González, I., Mathä, L., Steer, C. A., Ghaedi, M., Poon, G. F. T., & Takei, F. (2016) · Immunity · doi:10.1016/j.immuni.2016.06.017 · Cited by 305
Sexual Dimorphism in Innate Immunity: The Role of Sex Hormones and Epigenetics
Shepherd, R., Cheung, A. S., Pang, K. C., Saffery, R., & Novakovic, B. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.604000 · Cited by 322
Interconnections between Inflammageing and Immunosenescence during Ageing
Teissier, T., Boulanger, É., & Cox, L. S. (2022) · Cells · doi:10.3390/cells11030359 · Cited by 323
Epigenetic memory of coronavirus infection in innate immune cells and their progenitors
Cheong, J.-G., Ravishankar, A., Sharma, S., Parkhurst, C. N., Grassmann, S. A., Wingert, C. K., Laurent, P., Ma, S., Paddock, L., Miranda, I. C., et al. (2023) · Cell · doi:10.1016/j.cell.2023.07.019 · Cited by 309
Biering-Sørensen, S. R., Aaby, P., Lund, N., Monteiro, I., Jensen, K. J., Eriksen, H. B., Schaltz‐Buchholzer, F., Jørgensen, A. S. P., Rodrigues, A., Fisker, A. B., et al. (2017) · Clinical Infectious Diseases · doi:10.1093/cid/cix525 · Cited by 294
Franceschi, C., Salvioli, S., Garagnani, P., de Eguileor, M., Monti, D., & Capri, M. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00982 · Cited by 290
Innate immune memory: An evolutionary perspective
Gourbal, B., Pinaud, S., Beckers, G. J. M., van der Meer, J. W. M., Conrath, U., & Netea, M. G. (2018) · Immunological Reviews · doi:10.1111/imr.12647 · Cited by 292
Self-citationCrișan, T. O., Cleophas, M. C. P., Oosting, M., Lemmers, H., Toenhake-Dijkstra, H., Netea, M. G., Jansen, T., & Joosten, L. A. B. (2015) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2014-206564 · Cited by 289
Self-citationEpigenetics and Trained Immunity
van der Heijden, C. D. C. C., Noz, M. P., Joosten, L. A. B., Netea, M. G., Riksen, N. P., & Keating, S. T. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7310 · Cited by 295
Self-citationThe single-cell epigenomic and transcriptional landscape of immunity to influenza vaccination
Wimmers, F., Donato, M., Kuo, A. J., Ashuach, T., Gupta, S., Li, C., Dvorak, M., Foecke, M. H., Chang, S. E., Hagan, T., et al. (2021) · Cell · doi:10.1016/j.cell.2021.05.039 · Cited by 275
Sánchez‐Ramón, S., Conejero, L., Netea, M. G., Sancho, D., Palomares, Ó., & Subiza, J. L. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02936 · Cited by 271
Self-citationUrate‐induced immune programming: Consequences for gouty arthritis and hyperuricemia
Cabău, G., Crișan, T. O., Klück, V., Popp, R. A., & Joosten, L. A. B. (2019) · Immunological Reviews · doi:10.1111/imr.12833 · Cited by 267
Self-citationInnate cell communication kick-starts pathogen-specific immunity
Rivera, A., Siracusa, M. C., Yap, G. S., & Gause, W. C. (2016) · Nature Immunology · doi:10.1038/ni.3375 · Cited by 277
What Have We Learnt about BCG Vaccination in the Last 20 Years?
Dockrell, H. M., & Smith, S. G. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01134 · Cited by 269
Combating Implant Infections: Shifting Focus from Bacteria to Host
Yavari, S. A., Castenmiller, S. M., van Strijp, J. A. G., & Croes, M. (2020) · Advanced Materials · doi:10.1002/adma.202002962 · Cited by 258
Harnessing the beneficial heterologous effects of vaccination
Goodridge, H. S., Ahmed, S., Curtis, N. C., Kollmann, T. R., Levy, O., Netea, M. G., Pollard, A. J., van Crevel, R., & Wilson, C. B. (2016) · Nature reviews. Immunology · doi:10.1038/nri.2016.43 · Cited by 260
Self-citationLeentjens, J., Kox, M., Stokman, R., Gerretsen, J., Diavatopoulos, D. A., van Crevel, R., Rimmelzwaan, G. F., Pickkers, P., & Netea, M. G. (2015) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiv332 · Cited by 255
Self-citationPriming Microglia for Innate Immune Memory in the Brain
Neher, J. J., & Cunningham, C. M. (2019) · Trends in Immunology · doi:10.1016/j.it.2019.02.001 · Cited by 263
Monocyte and macrophage immunometabolism in atherosclerosis
Groh, L. A., Keating, S. T., Joosten, L. A. B., Netea, M. G., & Riksen, N. P. (2017) · Seminars in Immunopathology · doi:10.1007/s00281-017-0656-7 · Cited by 258
Self-citation100 years of Mycobacterium bovis bacille Calmette-Guérin
Lange, C. G., Aaby, P., Behr, M. A., Donald, P. R., Kaufmann, S. H. E., Netea, M. G., & Mandalakas, A. M. (2021) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(21)00403-5 · Cited by 268
Self-citationInnate immune memory: towards a better understanding of host defense mechanisms
Quintin, J., Cheng, S., van der Meer, J. W., & Netea, M. G. (2014) · Current Opinion in Immunology · doi:10.1016/j.coi.2014.02.006 · Cited by 259
Self-citationTrained Immunity: An Ancient Way of Remembering
Netea, M. G., & van der Meer, J. W. M. (2017) · Cell Host & Microbe · doi:10.1016/j.chom.2017.02.003 · Cited by 259
Self-citationKieler, M., Hofmann, M., & Schabbauer, G. (2021) · FEBS Journal · doi:10.1111/febs.15715 · Cited by 250
Dectin-1 Signaling Update: New Perspectives for Trained Immunity
Mata-Martínez, P., Bergón-Gutiérrez, M., & del Fresno, C. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.812148 · Cited by 258
Potential Role of Gut Microbiota in Induction and Regulation of Innate Immune Memory
Negi, S., Das, D. K., Pahari, S., Nadeem, S., & Agrewala, J. N. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02441 · Cited by 247
Bekkering, S., van den Munckhof, I., Nielen, T. M., Lamfers, E. J. P., Dinarello, C. A., Rutten, J. H. W., Graaf, J. D., Joosten, L. A. B., Netea, M. G., Gomes, M. E. R., et al. (2016) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2016.10.019 · Cited by 238
Self-citationNon-specific effects of vaccines: Current evidence and potential implications
de Bree, L. C. J., Koeken, V. A. C. M., Joosten, L. A. B., Aaby, P., Benn, C. S., van Crevel, R., & Netea, M. G. (2018) · Seminars in Immunology · doi:10.1016/j.smim.2018.06.002 · Cited by 233
Self-citationBuffen, K., Oosting, M., Quintin, J., Ng, A., Kleinnijenhuis, J., Kumar, V., van de Vosse, E., Wijmenga, C., van Crevel, R., Oosterwijk, E., et al. (2014) · PLoS Pathogens · doi:10.1371/journal.ppat.1004485 · Cited by 235
Self-citationCultural Differences in Academic Rhetoric.: A Textlinguistic Study.
Mauranen, A. (1993) · Cited by 477
The Regulation of Inflammation by Innate and Adaptive Lymphocytes
Cronkite, D. A., & Strutt, T. M. (2018) · Journal of Immunology Research · doi:10.1155/2018/1467538 · Cited by 239
Priem, B., van Leent, M. M. T., Teunissen, A. J. P., Sofias, A. M., Mourits, V. P., Willemsen, L., Klein, E. D., Oosterwijk, R. S., Meerwaldt, A. E., Munitz, J., et al. (2020) · Cell · doi:10.1016/j.cell.2020.09.059 · Cited by 222
Self-citationFülöp, T., Larbi, A., & Witkowski, J. M. (2019) · Gerontology · doi:10.1159/000497375 · Cited by 221
Outcomes of controlled human malaria infection after BCG vaccination
Walk, J., de Bree, L. C. J., Graumans, W., Stoter, R., van Gemert, G., van de Vegte‐Bolmer, M., Teelen, K., Hermsen, C. C., Arts, R. J. W., Behet, M. C., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-08659-3 · Cited by 219
Self-citationImmunometabolic circuits in trained immunity
Arts, R. J. W., Joosten, L. A. B., & Netea, M. G. (2016) · Seminars in Immunology · doi:10.1016/j.smim.2016.09.002 · Cited by 228
Self-citationTrained immunity: adaptation within innate immune mechanisms
Domínguez‐Andrés, J., dos Santos, J. C., Bekkering, S., Mulder, W. J. M., van der Meer, J. W. M., Riksen, N. P., Joosten, L. A. B., & Netea, M. G. (2022) · Physiological Reviews · doi:10.1152/physrev.00031.2021 · Cited by 227
Self-citationTrained innate immunity as underlying mechanism for the long-term, nonspecific effects of vaccines
Blok, B. A., Arts, R. J. W., van Crevel, R., Benn, C. S., & Netea, M. G. (2015) · Journal of Leukocyte Biology · doi:10.1189/jlb.5ri0315-096r · Cited by 211
Self-citationde Castro, M. J., Pardo‐Seco, J., & Martinón‐Torres, F. (2015) · Clinical Infectious Diseases · doi:10.1093/cid/civ144 · Cited by 209
Interferon stimulation creates chromatin marks and establishes transcriptional memory
Kamada, R., Yang, W., Zhang, Y., Patel, M. C., Yang, Y., Ouda, R., Dey, A., Wakabayashi, Y., Sakaguchi, K., Fujita, T., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1720930115 · Cited by 206
Therapeutic host-directed strategies to improve outcome in tuberculosis
Young, C., Walzl, G., & du Plessis, N. (2019) · Mucosal Immunology · doi:10.1038/s41385-019-0226-5 · Cited by 202
Trained immunity as a molecular mechanism for BCG immunotherapy in bladder cancer
van Puffelen, J. H., Keating, S. T., Oosterwijk, E., van der Heijden, A. G., Netea, M. G., Joosten, L. A. B., & Vermeulen, S. H. H. M. (2020) · Nature Reviews Urology · doi:10.1038/s41585-020-0346-4 · Cited by 207
Self-citationVaccinology: time to change the paradigm?
Benn, C. S., Fisker, A. B., Rieckmann, A., Sørup, S., & Aaby, P. (2020) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(19)30742-x · Cited by 202
Innate Immune Memory in Invertebrate Metazoans: A Critical Appraisal
Melillo, D., Marino, R., Italiani, P., & Boraschi, D. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01915 · Cited by 213
The Cellular and Molecular Basis of Translational Immunometabolism
Norata, G. D., Caligiuri, G., Chavakis, T., Matarese, G., Netea, M. G., Nicoletti, A., O'Neill, L. A. J., & Marelli‐Berg, F. M. (2015) · Immunity · doi:10.1016/j.immuni.2015.08.023 · Cited by 197
Self-citationLong-lived effects of administering β-glucans: Indications for trained immunity in fish
Petit, J., & Wiegertjes, G. F. (2016) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2016.03.003 · Cited by 196
Induction of memory-like dendritic cell responses in vivo
Hole, C. R., Wager, C. M. L., Castro-Lopez, N., Campuzano, A., Cai, H., Wozniak, K. L., Wang, Y., & Wormley, F. L. (2019) · Nature Communications · doi:10.1038/s41467-019-10486-5 · Cited by 199
Stienstra, R., Netea-Maier, R. T., Riksen, N. P., Joosten, L. A. B., & Netea, M. G. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.06.001 · Cited by 206
Self-citationClonal expansion and epigenetic inheritance of long-lasting NK cell memory
Rückert, T., Lareau, C. A., Mashreghi, M., Ludwig, L. S., & Romagnani, C. (2022) · Nature Immunology · doi:10.1038/s41590-022-01327-7 · Cited by 194
Trained immunity in newborn infants of HBV-infected mothers
Hong, M. L. W., Sandalova, E., Low, D. H. P., Gehring, A. J., Fieni, S., Amadei, B., Urbani, S., Chong, Y. S., Guccione, E., & Bertoletti, A. (2015) · Nature Communications · doi:10.1038/ncomms7588 · Cited by 195
Yoshida, K., Maekawa, T., Zhu, Y., Renard-Guillet, C., Chatton, B., Inoue, K., Uchiyama, T., Ishibashi, K., Yamada, T., Ohno, N., et al. (2015) · Nature Immunology · doi:10.1038/ni.3257 · Cited by 198
Metadata
- Authors
- Kleinnijenhuis, J., Quintin, J., Preijers, F., Joosten, L. A. B., Ifrim, D. C., Saeed, S., Jacobs, C., van Loenhout, J., de Jong, D., Stunnenberg, H. G., Xavier, R. J., van der Meer, J. W. M., van Crevel, R., & Netea, M. G.
- Affiliations
- Radboud University Medical Center (NL)
- Department of Medicine,
- Radboud University Nijmegen (NL)
- Public Health Office GGD, Nijmegen, The Netherlands;
- Department of Gastroenterology, Radboud University Nijmegen Medical Centre, 6525 GA Nijmegen, The Netherlands;
- Broad Institute (US)
- ORCID
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2012-09-17
- Volume
- 109
- Issue
- 43
- Pages
- 17537-17542
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC3491454
- OpenAlex
- W2059403792
- Cited by
- 1,728
- References
- 35
- Citations by year
- 2026: 139 · 2025: 174 · 2024: 127 · 2023: 150 · 2022: 170 · 2021: 226 · 2020: 204 · 2019: 118 · 2018: 119 · 2017: 79 · 2016: 74 · 2015: 68 · 2014: 51 · 2013: 25 · 2012: 2
- FWCI
- 20.34
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Radboud Repository (Radboud University) (submittedVersion)
- HAL (submittedVersion)
- Funders
- Leona M. and Harry B. Helmsley Charitable Trust
- Higher Education Commision, Pakistan
- National Institutes of Health (DK 043351)
- National Institute of Allergy and Infectious Diseases (AI 062773, R01AI062773)
- National Institute of Diabetes and Digestive and Kidney Diseases ((DK043351, R01DK083756, DK 83756, P30DK043351)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune responses and vaccinations
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Keywords
- BCG vaccine, trained immunity, NOD2, epigenetic reprogramming, histone H3 lysine 4 trimethylation, monocytes, innate immunity, interferon-gamma, TNF-α, IL-1β, TLR4, CD11b, candidiasis, BCG vaccination, SCID mice
- MeSH terms
- Adult, B-Lymphocytes, Base Sequence, BCG Vaccine, Histones, Humans, Methylation, Monocytes, T-Lymphocytes, Polymerase Chain Reaction, DNA Primers, Epigenesis, Genetic, Chromatin Immunoprecipitation, Nod2 Signaling Adaptor Protein
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