Epigenetic programming of monocyte-to-macrophage differentiation and trained innate immunity

Macrophage plasticity and polarization: in vivo veritas

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Monocyte and macrophage heterogeneity

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Macrophage biology in development, homeostasis and disease

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Development of Monocytes, Macrophages, and Dendritic Cells

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The accessible chromatin landscape of the human genome

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Regulation and Function of NF-κB Transcription Factors in the Immune System

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Histone modifications at human enhancers reflect global cell-type-specific gene expression

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Transcriptional Profiling of the Human Monocyte-to-Macrophage Differentiation and Polarization: New Molecules and Patterns of Gene Expression

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A unique chromatin signature uncovers early developmental enhancers in humans

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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

Trained immunity and immune priming in plants and invertebrates

Kurtz, J., Andino, R., Boraschi, D., Contreras-Garduño, J. A., Kachroo, A., Khan, I., Lanz‐Mendoza, H., Mukherjee, K., Peuß, R., & Ton, J. (2025) · eLife · doi:10.7554/elife.106597 · Cited by 25

Sequential changes in histone modifications shape transcriptional responses underlying microglia polarization by glioma

Maleszewska, M., Steranka, A., Śmiech, M., Kaza, B., Pilanc, P., Dąbrowski, M., & Kaminska, B. (2020) · Glia · doi:10.1002/glia.23887 · Cited by 24

Mitochondrial Signature in Human Monocytes and Resistance to Infection in C. elegans During Fumarate-Induced Innate Immune Training

Pérez-Hernández, C. A., Kern, C. C., Butkevičiūtė, E., McCarthy, E., Dockrell, H. M., Moreno‐Altamirano, M. M. B., Aguilar‐López, B. A., Bhosale, G., Wang, H., Gems, D., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01715 · Cited by 19

The role of sirtuin 1 on the induction of trained immunity

Mourits, V. P., Helder, L. S., Matzaraki, V., Koeken, V. A. C. M., Groh, L. A., de Bree, L. C. J., Moorlag, S. J. C. F. M., van der Heijden, C. D. C. C., Keating, S. T., van Puffelen, J. H., et al. (2021) · Cellular Immunology · doi:10.1016/j.cellimm.2021.104393 · Cited by 21

Heat inactivated mycobacteria, alpha‐Gal and zebrafish: Insights gained from experiences with two promising trained immunity inductors and a validated animal model

Juste, R. A., Ferreras‐Colino, E., de la Fuente, J., Domínguez, M., Risalde, M. Á., Domı́nguez, L., Cabezas‐Cruz, A., & Gortázar, C. (2022) · Immunology · doi:10.1111/imm.13529 · Cited by 21

Immunological hyporesponsiveness in tuberculosis: The role of mycobacterial glycolipids

Correia‐Neves, M., Nigou, J., Mousavian, Z., Sundling, C., & Källenius, G. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1035122 · Cited by 23

Artificial cells delivering itaconic acid induce anti-inflammatory memory-like macrophages to reverse acute liver failure and prevent reinjury

Yin, N., Zhang, W., Sun, X., Wei, R., Yang, Q., He, F., Li, C., Guo, L., & Feng, M. (2023) · Cell Reports Medicine · doi:10.1016/j.xcrm.2023.101132 · Cited by 23

The mechanisms and factors that induce trained immunity in arthropods and mollusks

Zhao, M., Lin, Z., Zheng, Z., Yao, D., Yang, S., Zhao, Y., Chen, X., Aweya, J. J., & Zhang, Y. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1241934 · Cited by 22

Macrophage memory: Types, mechanisms, and its role in health and disease

Fang, X., Li, Z., Liu, C., Mor, G., & Liao, A. (2023) · Immunology · doi:10.1111/imm.13697 · Cited by 23

Innate memory training

Bordon, Y. (2014) · Nature reviews. Immunology · doi:10.1038/nri3759 · Cited by 21

Master and commander: epigenetic regulation of macrophages

Netea, M. G., & Joosten, L. A. B. (2016) · Cell Research · doi:10.1038/cr.2016.5 · Cited by 21

The preventable efficacy of β-glucan against leptospirosis

Wang, J., Jin, Z., Zhang, W., Xie, X., Song, N., Lv, T., Wu, D., & Cao, Y. (2019) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0007789 · Cited by 22

BCG immunomodulation: From the ‘hygiene hypothesis’ to COVID-19

Moulson, A., & Av-Gay, Y. (2020) · Immunobiology · doi:10.1016/j.imbio.2020.152052 · Cited by 23

Systems Biological Analysis of Immune Response to Influenza VaccinationPreprint

Cortese, M., Sherman, A. C., Rouphael, N., & Pulendran, B. (2020) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a038596 · Cited by 22

Discovering adaptive features of innate immune memory

Sadeghi, M., & Divangahi, M. (2024) · Immunological Reviews · doi:10.1111/imr.13328 · Cited by 19

Hormesis as an adaptive response to infection

Bauer, M. W., Ermolaeva, M., Singer, M., Wetzker, R., & Soares, M. P. (2024) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2024.04.012 · Cited by 20

Novel Strategies for Preventing Fungal Infections—Outline

Agbadamashi, D. J., & Price, C. L. (2025) · Pathogens · doi:10.3390/pathogens14020126 · Cited by 21

Metabolic adaptations driving innate immune memory: mechanisms and therapeutic implications

Hao, D., McBride, M. A., Bohannon, J. K., Hernandez, A., Klein, B., Williams, D. L., & Sherwood, E. R. (2025) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiaf037 · Cited by 21

DNA methylation and histone modifications drive the trained immunity duration

Liu, M., Shen, X., & Xu, L. (2025) · Trends in Immunology · doi:10.1016/j.it.2025.10.004 · Cited by 20

Oncogene-induced maladaptive activation of trained immunity in the pathogenesis and treatment of Erdheim-Chester disease

Molteni, R., Biavasco, R., Stefanoni, D., Nemkov, T. G., Domínguez‐Andrés, J., Arts, R. J. W., Merelli, I., Mazza, D., Zambrano, S., Panigada, M., et al. (2021) · Blood · doi:10.1182/blood.2020009594 · Cited by 20

Transcriptional, Epigenetic, and Functional Reprogramming of Monocytes From Non-Human Primates Following Chronic Alcohol Drinking

Lewis, S. A., Sureshchandra, S., Doratt, B. M., Jimenez, V. A., Stull, C., Grant, K. A., & Messaoudi, I. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.724015 · Cited by 20

Activation of epigenetic regulator KDM6B by Salmonella Typhimurium enables chronic infections

Rana, S., Maurya, S., Mohapatra, G., Singh, S., Babar, R., Chandrasekhar, H., Chamoli, G., Rathore, D. K., Kshetrapal, P., & Srikanth, C. V. (2021) · Gut Microbes · doi:10.1080/19490976.2021.1986665 · Cited by 21

Macrophage plasticity in Duchenne muscular dystrophy: a nexus of pathological remodelling with therapeutic implications

Petrof, B. J. (2021) · The Journal of Physiology · doi:10.1113/jp281673 · Cited by 23

Hematopoietic Progenitors and the Bone Marrow Niche Shape the Inflammatory Response and Contribute to Chronic Disease

Xu, Y., Murphy, A. J., & Fleetwood, A. J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23042234 · Cited by 23

Inhibition of Histone H3 Lysine-27 Demethylase Activity Relieves Rheumatoid Arthritis Symptoms via Repression of IL6 Transcription in Macrophages

Zhao, Z., Zhang, Y., Gao, D., Zhang, Y., Han, W., Xu, X., Song, Q., Zhao, C., & Yang, J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.818070 · Cited by 21

Systemic Inflammation Causes Microglial Dysfunction With a Vascular AD phenotype

Bathini, P., Dupanloup, I., Zenaro, E., Terrabuio, E., Fischer, A., Ballabani, E., Doucey, M., & Alberi, L. A. (2022) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2022.100568 · Cited by 22

Trained immunity in monocyte/macrophage: Novel mechanism of phytochemicals in the treatment of atherosclerotic cardiovascular disease

Wang, J., Liu, Y., Hu, J., & Chen, C. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1109576 · Cited by 24

Inflammation and epithelial repair predict mortality, hospital readmission, and growth recovery in complicated severe acute malnutrition

Sturgeon, J. P., Tome, J., Dumbura, C., Majo, F. D., Ngosa, D., Mutasa, K., Zyambo, K., Besa, E. C., Chandwe, K., Kapoma, C., et al. (2024) · Science Translational Medicine · doi:10.1126/scitranslmed.adh0673 · Cited by 20

Leishmania braziliensis enhances monocyte responses to promote anti-tumor activity

dos Santos, J. C., Moreno, M., Teufel, L. U., Chilibroste, S., Keating, S. T., Groh, L. A., Domínguez‐Andrés, J., Williams, D. L., Ma, Z., Lowman, D. W., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.113932 · Cited by 21

I Remember You: Epigenetic Priming in Epithelial Stem Cells

Novakovic, B., & Stunnenberg, H. G. (2017) · Immunity · doi:10.1016/j.immuni.2017.12.005 · Cited by 20

Epigenetics and Malaria Susceptibility/Protection: A Missing Piece of the Puzzle

Arama, C., Quin, J. E., Kouriba, B., Farrants, A. Ö., Troye‐Blomberg, M., & Doumbo, O. K. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01733 · Cited by 20

Macrophage polarization by phytotherapy in the tumor microenvironment

Saeedifar, A. M., Mosayebi, G., Ghazavi, A., Bushehri, R. H., & Ganji, A. (2021) · Phytotherapy Research · doi:10.1002/ptr.7058 · Cited by 19

COVID-19: A model correlating BCG vaccination to protection from mortality implicates trained immunityPreprint

Green, C. M., Fanucchi, S., Domínguez‐Andrés, J., Fok, E. T., Moorlag, S. J. C. F. M., Negishi, Y., Joosten, L. A. B., Netea, M. G., & Mhlanga, M. M. (2020) · medRxiv · doi:10.1101/2020.04.10.20060905 · Cited by 20

IgE versus IgG and IgA : Differential roles of allergen‐specific antibodies in sensitization, tolerization, and treatment of allergies

Knol, E. F., & van Neerven, R. J. J. (2024) · Immunological Reviews · doi:10.1111/imr.13386 · Cited by 19

IRF1 cooperates with ISGF3 or GAF to form innate immune de novo enhancers in macrophages

Chavez, C., Lin, K., Malveaux, A., Gorin, A. M., Brizuela, S., Cheng, Q. J., & Hoffmann, A. (2025) · Science Signaling · doi:10.1126/scisignal.ado8860 · Cited by 19

Unraveling the metabolic‒epigenetic nexus: a new frontier in cardiovascular disease treatment

Ouyang, J., Wu, D.-D., Gan, Y., Tang, Y., Wang, H., & Huang, J. (2025) · Cell Death and Disease · doi:10.1038/s41419-025-07525-z · Cited by 21

Innate immune memory: The evolving role of macrophages in therapy

Damani‐Yokota, P., & Khanna, K. M. (2025) · eLife · doi:10.7554/elife.108276 · Cited by 22

The Impact of Type 1 Interferons on Alveolar Macrophage Tolerance and Implications for Host Susceptibility to Secondary Bacterial Pneumonia

Connolly, E., & Hussell, T. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00495 · Cited by 18

Resolving trained immunity with systems biology

Koeken, V. A. C. M., van Crevel, R., Netea, M. G., & Li, Y. (2021) · European Journal of Immunology · doi:10.1002/eji.202048882 · Cited by 19

Echinacea purpurea (L.) Moench treatment of monocytes promotes tonic interferon signaling, increased innate immunity gene expression and DNA repeat hypermethylated silencing of endogenous retroviral sequences

Declerck, K., Perez-Novo, C. A., Grielens, L., Camp, G. V., Suter, A., & Berghe, W. V. (2021) · BMC Complementary Medicine and Therapies · doi:10.1186/s12906-021-03310-5 · Cited by 20

PTIP governs NAD+ metabolism by regulating CD38 expression to drive macrophage inflammation

Wang, Q., Hu, J., Han, G., Wang, P., Li, S., Chang, J.-W., Gao, K., Yin, R., Li, Y., Zhang, T., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110603 · Cited by 19

Efficacy of Candida dubliniensis and Fungal β-Glucans in Inducing Trained Innate Immune Protection Against Inducers of Sepsis

Harriett, A. J., Esher, S. K., Lilly, E. A., Fidel, P. L., & Noverr, M. C. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.898030 · Cited by 19

Innate Immune Memory in Macrophages

Maheshwari, A. (2023) · Newborn · doi:10.5005/jp-journals-11002-0058 · Cited by 18

TLR7 Activation in M-CSF-Dependent Monocyte-Derived Human Macrophages Potentiates Inflammatory Responses and Prompts Neutrophil Recruitment

Simón‐Fuentes, M., Herrero, C., Acero-Riaguas, L., Nieto, C., Lasala, F., Labiod, N., Luczkowiak, J., Alonso, B., Delgado, R. B., Colmenares, M., et al. (2023) · Journal of Innate Immunity · doi:10.1159/000530249 · Cited by 21

Linking Mechanisms of Vitamin D Signaling with Multiple Sclerosis

Carlberg, C., & Mycko, M. P. (2023) · Cells · doi:10.3390/cells12192391 · Cited by 22

Bacteria- and fungus-derived PAMPs induce innate immune memory via similar functional, metabolic, and transcriptional adaptations

McBride, M. A., Stothers, C. L., Fensterheim, B. A., Burelbach, K. R., Owen, A. M., Hernandez, A., Bohannon, J. K., Patil, N. K., Ali, S., Dalal, S., et al. (2023) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiad120 · Cited by 19

Acid ceramidase regulates innate immune memory

Rother, N., Yanginlar, C., Prévot, G., Jonkman, I., Jacobs, M. M. E., van Leent, M. M. T., van Heck, J., Matzaraki, V., Azzun, A., Morlà‐Folch, J., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113458 · Cited by 22

Friends to remember: innate immune memory regulation by the microbiota

Pellón, A., Palacios, A., Abecia, L., Rodrı́guez, H., & Anguíta, J. (2025) · Trends in Microbiology · doi:10.1016/j.tim.2024.12.002 · Cited by 20

A Transcription Factor Pulse Can Prime Chromatin for Heritable Transcriptional Memory

Badeaux, A. I., Collombet, S., Laurent, B., van Oevelen, C. J. C., Chin, K., Thieffry, D., Graf, T., & Shi, Y. (2016) · Molecular and Cellular Biology · doi:10.1128/mcb.00372-16 · Cited by 20

Intestinal parasitic infection alters bone marrow derived dendritic cell inflammatory cytokine production in response to bacterial endotoxin in a diet-dependent manner

Burgess, S. L., Oka, A., Liu, B., Bolick, D. T., Oakland, D. N., Guerrant, R. L., & Bartelt, L. A. (2019) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0007515 · Cited by 18

The Methyl-CpG-Binding Protein Mbd2 Regulates Susceptibility to Experimental Colitis via Control of CD11c+ Cells and Colonic Epithelium

Jones, G., Brown, S. L., Phythian‐Adams, A., Ivens, A. C., Cook, P. C., & MacDonald, A. S. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00183 · Cited by 19

Latitudinal and longitudinal regulation of tissue macrophages in inflammatory diseases

He, X.-Y., Tan, S., Shao, Z., & Wang, X. (2021) · Genes & Diseases · doi:10.1016/j.gendis.2021.06.007 · Cited by 20

Trained Immunity Provides Long-Term Protection against Bacterial Infections in Channel Catfish

Petrie-Hanson, L., & Peterman, A. E. (. (2022) · Pathogens · doi:10.3390/pathogens11101140 · Cited by 19

Modelling Microglial Innate Immune Memory In Vitro: Understanding the Role of Aerobic Glycolysis in Innate Immune Memory

Towriss, M., MacVicar, B. A., & Ciernia, A. V. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24108967 · Cited by 19

Infection-induced trained immunity: a twist in paradigm of innate host defense and generation of immunological memory

Bahl, A., Pandey, S., Rakshit, R., Kant, S., & Tripathi, D. (2024) · Infection and Immunity · doi:10.1128/iai.00472-24 · Cited by 22

Innate immune memory in macrophage differentiation and cardiovascular diseases

Nakayama, Y., & Fujiu, K. (2025) · Inflammation and Regeneration · doi:10.1186/s41232-025-00382-5 · Cited by 22

Inflammatory genes TNFα and IL6 display no signs of increased H3K4me3 in circulating monocytes from untreated rheumatoid arthritis patients

Messemaker, T. C., Mikkers, H. M. M., Huizinga, T. W. J., Toes, R. E. M., Mil, A. H. M. V. D. H., & Kurreeman, F. A. S. (2017) · Genes and Immunity · doi:10.1038/gene.2017.20 · Cited by 18

A trade-off switch of two immunological memories in Caenorhabditis elegans reinfected by bacterial pathogens

Yan, J., Zhao, N., Yang, Z., Li, Y., Bai, H., Zou, W., Zhang, K., & Huang, X. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra120.013923 · Cited by 18

Alterations in Chromatin Structure and Function in the Microglia

Fujita, Y., & Yamashita, T. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.626541 · Cited by 22

Histone H3 lysine 27 acetylation profile undergoes two global shifts in undernourished children and suggests altered one-carbon metabolism

Kupkova, K., Shetty, S. J., Haque, R., Petri, W. A., & Auble, D. (2021) · Clinical Epigenetics · doi:10.1186/s13148-021-01173-8 · Cited by 20

Ischemic-Trained Monocytes Improve Arteriogenesis in a Mouse Model of Hindlimb Ischemia

Falero-Díaz, G., Barboza, C. D. A., Pires, F., Fanchin, M., Ling, J., Zigmond, Z. M., Griswold, A. J., Martinez, L., Vázquez-Padrón, R. I., Velazquez, O. C., et al. (2021) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.121.317197 · Cited by 18

T-cell deficiency and hyperinflammatory monocyte responses associate with Mycobacterium avium complex lung disease

Arlehamn, C. S. L., Benson, B., Kuan, R., Dill‐McFarland, K. A., Peterson, G. J., Paul, S., Nguyen, F. K., Gilman, R. H., Saito, M., Taplitz, R., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1016038 · Cited by 18

Streptococcus pneumoniae drives specific and lasting Natural Killer cell memory

Camarasa, T., Torné, J., Chevalier, C., Raşid, O., & Hamon, M. A. (2023) · PLoS Pathogens · doi:10.1371/journal.ppat.1011159 · Cited by 18

The Aryl Hydrocarbon Receptor Regulates Epidermal Differentiation through Transient Activation of TFAP2A

Smits, J. P. H., Qu, J., Pardow, F., van den Brink, N. J. M., Rodijk‐Olthuis, D., van Vlijmen‐Willems, I. M. J. J., van Heeringen, S. J., Zeeuwen, P. L. J. M., Schalkwijk, J., Zhou, H., et al. (2024) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2024.01.030 · Cited by 18

Genetic and epigenetic dysregulation of innate immune mechanisms in autoinflammatory diseases

Pich, L. M. M., Ziogas, A., & Netea, M. G. (2024) · FEBS Journal · doi:10.1111/febs.17116 · Cited by 19

Porphyromonas gingivalis ‐Lipopolysaccharide Induced Gingival Fibroblasts Trained Immunity Sustains Inflammation in Periodontitis

Liu, J., Tian, H., Ju, J., Nie, F., Yin, Q., Zhao, J., Wang, S., Guo, H., & Yang, P. (2024) · Journal of Periodontal Research · doi:10.1111/jre.13372 · Cited by 19

Effect of Schistosoma mansoni Infection on Innate and HIV-1-Specific T-Cell Immune Responses in HIV-1-Infected Ugandan Fisher Folk

Obuku, A. E., Asiki, G., Abaasa, A. M., Ssonko, I., Harari, A., van Dam, G. J., Corstjens, P. L. A. M., Joloba, M. L., Ding, S.-W., Mpendo, J., et al. (2016) · AIDS Research and Human Retroviruses · doi:10.1089/aid.2015.0274 · Cited by 18

The multifaceted interplay between lipids and epigenetics

Dekkers, K. F., Slagboom, P. E., Jukema, J. W., & Heijmans, B. T. (2016) · Current Opinion in Lipidology · doi:10.1097/mol.0000000000000301 · Cited by 18

Cracking the Vaccine Code in Tuberculosis

Divangahi, M., & Behr, M. A. (2017) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201707-1489pp · Cited by 20

Emerging Concepts in Innate Immunity

Pelka, K., & Nardo, D. D. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-7519-8_1 · Cited by 19

Tumor Associated Macrophages as Therapeutic Targets for Breast Cancer

Lao, L., Fan, S., & Song, E. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-981-10-6020-5_16 · Cited by 19

Train to Lose: Innate Immune Memory in Metaflammation

Charles‐Messance, H., & Sheedy, F. J. (2020) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201900480 · Cited by 18

On Deep Landscape Exploration of COVID-19 Patients Cells and Severity Markers

Vázquez-Jiménez, A., de León, U. A.-P., Matadamas-Guzman, M. L., Muciño-Olmos, E. A., Martínez-López, Y. E., Escobedo-Tapia, T., & Reséndis-Antonio, O. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.705646 · Cited by 18

One genome, many cell states: epigenetic control of innate immunity

Fraschilla, I. R., Amatullah, H., & Jeffrey, K. L. (2022) · Current Opinion in Immunology · doi:10.1016/j.coi.2022.102173 · Cited by 19

Developmental Control of NRAMP1 (SLC11A1) Expression in Professional Phagocytes

Cellier, M. F. (2017) · Biology · doi:10.3390/biology6020028 · Cited by 20

DNA Synthesis Is Activated in Mosquitoes and Human Monocytes During the Induction of Innate Immune Memory

Cime‐Castillo, J., Arts, R. J. W., Vargas, V., Moreno‐Torres, R., Hernández‐Martínez, S., Recio-Tótoro, B., Claudio-Piedras, F., Netea, M. G., & Lanz‐Mendoza, H. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02834 · Cited by 18

Trained Immunity and Autoimmune Disease: Did Eve Sin before Adam?

Berthelot, J., & Sibilia, J. (2018) · Joint Bone Spine · doi:10.1016/j.jbspin.2018.12.006 · Cited by 18

Temporal and Epigenetic Control of Plasticity and Fate Decision during CD8+T-Cell Memory DifferentiationPreprint

Pace, L. (2021) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a037754 · Cited by 19

Aspergillus-induced superoxide production by cystic fibrosis phagocytes is associated with disease severity

Brunel, S. F., Willment, J. A., Brown, G. D., Devereux, G., & Warris, A. (2018) · ERJ Open Research · doi:10.1183/23120541.00068-2017 · Cited by 17

Does the Microbiota Composition Influence the Efficacy of Colorectal Cancer Immunotherapy?

Lin, Y., Kong, D.-X., & Zhang, Y.-N. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.852194 · Cited by 17

Ethanol Consumption Induces Nonspecific Inflammation and Functional Defects in Alveolar Macrophages

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CD11c identifies microbiota and EGR2‐dependent MHCII+ serous cavity macrophages with sexually dimorphic fate in mice

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