Origins and Functional Specialization of Macrophages and of Conventional and Monocyte-Derived Dendritic Cells in Mouse Skin

Fate Mapping Analysis Reveals That Adult Microglia Derive from Primitive Macrophages

Ginhoux, F., Greter, M., Leboeuf, M., Nandi, S., See, P., Gokhan, S., Mehler, M. F., Conway, S. J., Ng, L. G., Stanley, E. R., et al. (2010) · Science · doi:10.1126/science.1194637 · Cited by 5,175

T cell receptor antagonist peptides induce positive selection.

Hogquist, K., Jameson, S., Heath, W., Howard, J. L., Bevan, M., & Carbone, F. (1994) · Cell · doi:10.1016/0092-8674(94)90169-4 · Cited by 3,252

A Lineage of Myeloid Cells Independent of Myb and Hematopoietic Stem Cells

Schulz, C., Perdiguero, E. G., Chorro, L., Szabo-Rogers, H., Cagnard, N., Kierdorf, K., Prinz, M., Wu, B., Jacobsen, S. E. W., Pollard, J. W., et al. (2012) · Science · doi:10.1126/science.1219179 · Cited by 2,578

CCR7 Coordinates the Primary Immune Response by Establishing Functional Microenvironments in Secondary Lymphoid Organs

Förster, R., Schubel, A., Breitfeld, D., Kremmer, E., Renner‐Müller, I., Wolf, E., & Lipp, M. (1999) · Cell · doi:10.1016/s0092-8674(00)80059-8 · Cited by 2,348

Gene-expression profiles and transcriptional regulatory pathways that underlie the identity and diversity of mouse tissue macrophages

the Immunological Genome Consortium, Gautier, E. L., Shay, T., Miller, J., Greter, M., Jakubzick, C., Ivanov, S., Helft, J., Chow, A., Elpek, K. G., et al. (2012) · Nature Immunology · doi:10.1038/ni.2419 · Cited by 1,972

Monocyte emigration from bone marrow during bacterial infection requires signals mediated by chemokine receptor CCR2

Serbina, N. V., & Pamer, E. G. (2006) · Nature Immunology · doi:10.1038/ni1309 · Cited by 1,658

Selective depletion of macrophages reveals distinct, opposing roles during liver injury and repair

Duffield, J. S., Forbes, S. J., Constandinou, C. M., Clay, S., Partolina, M., Vuthoori, S., Wu, S., Lang, R., & Iredale, J. P. (2005) · Journal of Clinical Investigation · doi:10.1172/jci200522675 · Cited by 1,649

Defective TCR expression in transgenic mice constructed using cDNA‐based α‐ and β‐chain genes under the control of heterologous regulatory elements

Barnden, M., Allison, J., Heath, W. R., & Carbone, F. (1998) · Immunology and Cell Biology · doi:10.1046/j.1440-1711.1998.00709.x · Cited by 1,491

Microglia emerge from erythromyeloid precursors via Pu.1- and Irf8-dependent pathways

Kierdorf, K., Erny, D., Goldmann, T., Sander, V., Schulz, C., Perdiguero, E. G., Wieghofer, P., Heinrich, A., Riemke, P., Hölscher, C., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3318 · Cited by 1,457

Impaired monocyte migration and reduced type 1 (Th1) cytokine responses in C-C chemokine receptor 2 knockout mice.

Boring, L., Gosling, J., Chensue, S. W., Kunkel, S. L., Farese, R. V., Broxmeyer, H. E., & Charo, I. F. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119798 · Cited by 1,096

Development of Pig Conventional Dendritic Cells From Bone Marrow Hematopoietic Cells in vitro

Li, Y., Puebla-Clark, L., Hernández, J., Díaz, I., & Mateu, E. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.553859 · Cited by 14

Harnessing the reverse cholesterol transport pathway to favor differentiation of monocyte-derived APCs and antitumor responses

Raccosta, L., Marinozzi, M., Costantini, S., Maggioni, D., Ferreira, L. M., Corna, G., Zordan, P., Sorice, A., Farinello, D., Bianchessi, S., et al. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-05620-7 · Cited by 15

Neutrophil-Driven M2-Like Macrophages Are Critical for Skin Fibrosis in a Systemic Sclerosis Model

Gong, P., Ding, Y., Li, W., Yang, J., Su, X., Tian, R., Zhou, Y., Wang, T., Jiang, J., Liu, R., et al. (2024) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2024.03.031 · Cited by 17

Bioelectronics in the brain–gut axis: focus on inflammatory bowel disease (IBD)

Stakenborg, N., & Boeckxstaens, G. E. (2021) · International Immunology · doi:10.1093/intimm/dxab014 · Cited by 14

IL‐13 in dermal type‐2 dendritic cell specialization: From function to therapeutic targeting

Lamiable, O., Brewerton, M., & Ronchese, F. (2022) · European Journal of Immunology · doi:10.1002/eji.202149677 · Cited by 15

Metabolites: deciphering the molecular language between DCs and their environment

Minarrieta, L., Ghorbani, P., Sparwasser, T. D., & Berod, L. (2016) · Seminars in Immunopathology · doi:10.1007/s00281-016-0609-6 · Cited by 15

Dermal CD207-Negative Migratory Dendritic Cells Are Fully Competent to Prime Protective, Skin Homing Cytotoxic T-Lymphocyte Responses

Hain, T., Melchior, F., Kamenjarin, N., Muth, S., Weslati, H., Clausen, B. E., Mahnke, K., Silva-Vilches, C., Schütze, K., Sohl, J., et al. (2018) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2018.08.022 · Cited by 14

The site of tumor development determines immunogenicity via temporal mobilization of antigen‐laden dendritic cells in draining lymph nodes

Joncker, N. T., Bettini, S., Boulet, D., Guiraud, M., & Guerder, S. (2015) · European Journal of Immunology · doi:10.1002/eji.201545797 · Cited by 19

Autofluorescence identifies highly phagocytic tissue-resident macrophages in mouse and human skin and cutaneous squamous cell carcinoma

Bourdely, P., Petti, L., Khou, S., Meghraoui, A., Elaldi, R., Cazareth, J., Mossadegh‐Keller, N., Boyer, J., Sieweke, M. H., Poissonnet, G., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.903069 · Cited by 13

Interleukin‐37 promotes DMBA/TPA skin cancer through SIGIRR‐mediated inhibition of glycolysis in CD103+DC cells

Zeng, F., Wang, X., Hu, Y., Wang, Z., Li, Y., Hu, J., Yu, J., Zhou, P., Teng, X., Zhou, H., et al. (2023) · MedComm · doi:10.1002/mco2.229 · Cited by 13

Diesel Exhaust Particle (DEP)-induced glucose intolerance is driven by an intestinal innate immune response and NLRP3 activation in mice

Bosch, A. J. T., Rohm, T. V., AlAsfoor, S., Low, A. J. Y., Baumann, Z., Parayil, N., Noreen, F., Roux, J., Meier, D. T., & Cavelti‐Weder, C. (2023) · Particle and Fibre Toxicology · doi:10.1186/s12989-023-00536-8 · Cited by 15

The dual role of cannabidiol on monocyte-derived dendritic cell differentiation and maturation

Pénzes, Z., Alimohammadi, S., Horváth, D., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1240800 · Cited by 13

The multivalency game ruling the biology of immunity

Aiassa, L. V., Battaglia, G., & Rizzello, L. (2023) · Biophysics Reviews · doi:10.1063/5.0166165 · Cited by 11

Overview of dendritic cell‐based vaccine development for leishmaniasis

Bagirova, M., Allahverdiyev, A., Abamor, E. Ş., Ullah, I., Kutluoğlu, G. C., Aydoğdu, M. O., ŞENTÜRK, H., & Ergenoglu, B. (2016) · Parasite Immunology · doi:10.1111/pim.12360 · Cited by 13

A Quantitative Approach to SIV Functional Latency in Brain Macrophages

Abreu, C. M., Shirk, E. N., Queen, S. E., Mankowski, J. L., Gama, L., & Clements, J. E. (2018) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-018-9803-8 · Cited by 13

The origins of resident macrophages in mammary gland influence the tumorigenesis of breast cancer

Yang, Y., Hou, J., Liu, J., Bhushan, S., & Wu, G. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.109047 · Cited by 14

Ongoing production of tissue-resident macrophages from hematopoietic stem cells in healthy adult macaques

Rahmberg, A. R., Wu, C., Shin, T., Hong, S. G., Pei, L., Markowitz, T. E., Hickman, H. D., Dunbar, C. E., & Brenchley, J. M. (2023) · Blood Advances · doi:10.1182/bloodadvances.2023011499 · Cited by 13

Isolation of Mouse Dendritic Cell Subsets and Macrophages from the Skin

Malosse, C., & Henri, S. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-3606-9_9 · Cited by 13

The impact of ischemia‐reperfusion injuries on skin resident murine dendritic cells

Goh, C. C., Evrard, M., Chong, S. Z., et al. (2018) · European Journal of Immunology · doi:10.1002/eji.201747347 · Cited by 13

Clearance of HBeAg and HBsAg of HBV in mice model by a recombinant HBV vaccine combined with GM-CSF and IFN-α as an effective therapeutic vaccine adjuvant

Zhao, W., Zhao, G., Zhang, S., Wang, X., Yu, X., & Wang, B. (2018) · Oncotarget · doi:10.18632/oncotarget.25789 · Cited by 13

Functional Specialization of Dendritic Cell Subsets

Heidkamp, G. F., Lehmann, C. H. K., Heger, L., Baransk, A., Hoffmann, A., Lühr, J. J., & Dudziak, D. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-394447-4.30076-1 · Cited by 13

Intragranuloma Accumulation and Inflammatory Differentiation of Neutrophils Underlie Mycobacterial ESX-1-Dependent Immunopathology

Lienard, J., Munke, K., Wulff, L., Silva, C. D., Vandamme, J., Laschanzky, K., Joeris, T., Agace, W. W., & Carlsson, F. (2023) · mBio · doi:10.1128/mbio.02764-22 · Cited by 13

The beneficial effects of ethanolic extract of Sargassum serratifolium in DNCB-induced mouse model of atopic dermatitis

Kim, M.-J., Ryu, H., Jeong, H. H., Van, J. Y., Hwang, J. Y., Kim, A.-R., Seo, J., Moon, K. M., Jung, W., & Lee, B. (2024) · Scientific Reports · doi:10.1038/s41598-024-62828-z · Cited by 14

The longitudinal characterization of immune responses in COVID-19 patients reveals novel prognostic signatures for disease severity, patients’ survival and long COVID

Noviello, M., LORENZO, R. D., Chimienti, R., Maugeri, N., de Lalla, C., Siracusano, G., Lorè, N. I., Rancoita, P. M. V., Cugnata, F., Tassi, E., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1381091 · Cited by 13

SMAC mimetic drives microglia phenotype and glioblastoma immune microenvironment

Snacel-Fazy, E., Soubéran, A., Grange, M., Joseph, K., Colin, C., Morando, P., Luche, H., Pagano, A., Brustlein, S., Debarbieux, F. C., et al. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-07056-z · Cited by 13

Sustained accumulation of antigen‐presenting cells after infection promotes local T‐cell immunity

Collins, N., Hochheiser, K., Carbone, F. R., & Gebhardt, T. (2017) · Immunology and Cell Biology · doi:10.1038/icb.2017.60 · Cited by 12

Prenatal Development and Function of Human Mononuclear Phagocytes

Miah, M., Goh, I., & Haniffa, M. A. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.649937 · Cited by 13

N-Linked Glycans Shape Skin Immune Responses during Arthritis and Myositis after Intradermal Infection with Ross River Virus

Tharmarajah, K., Everest‐Dass, A., Vider, J., Liu, X., Freitas, J. R., Mostafavi, H., Bettadapura, J., von Itzstein, M., West, N. P., Taylor, A., et al. (2022) · Journal of Virology · doi:10.1128/jvi.00999-22 · Cited by 13

Multiple sclerosis: Skin-induced antigen-specific immune tolerance

Wildner, P., & Selmaj, K. W. (2017) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2017.08.001 · Cited by 12

Engulfment of Hb‐activated platelets differentiates monocytes into pro‐inflammatory macrophages in PNH patients

Singhal, R., Chawla, S., Batra, H., Gupta, S., Ojha, A., Rathore, D. K., Seth, T., & Guchhait, P. (2018) · European Journal of Immunology · doi:10.1002/eji.201747449 · Cited by 12

Reciprocal regulation of fibroblast–macrophage equilibrium governs skin integrity

Vollmers, A. C., Wu, S. Z., Altieri, A., McCartney, E. E., Bender, H. S., Davidson, C. D., Lee, W. P., Zhang, J., Hu, C., Jeet, S., et al. (2026) · Nature Immunology · doi:10.1038/s41590-026-02434-5 · Cited by 16

Metabolic adaption of mucosal macrophages: Is metabolism a driver of persistence across tissues?

Bennett, C. L., & Perona‐Wright, G. (2023) · Mucosal Immunology · doi:10.1016/j.mucimm.2023.06.006 · Cited by 11

Polymer-Based Wound Dressings Loaded with Ginsenoside Rg3

Yang, J., Zhang, L., Peng, X., Zhang, S., Sun, S., Ding, Q., Ding, C., & Liu, W. (2023) · Molecules · doi:10.3390/molecules28135066 · Cited by 11

Guided monocyte fate to FRβ/CD163+ S1 macrophage antagonises atopic dermatitis via fibroblastic matrices in mouse hypodermis

Li, Y., Takaki, E., Ouchi, Y., & Tamai, K. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-024-05543-2 · Cited by 13

Macrophage Differentiation and Metabolic Adaptation in Mycobacterial Infections

Lößlein, A. K., & Henneke, P. (2025) · Annual Review of Immunology · doi:10.1146/annurev-immunol-082323-120757 · Cited by 14

Functional specialization of short-lived and long-lived macrophage subsets in human tonsils

Alaoui, L., Villar, J., Leclère, R., Gallou, S. L., Relouzat, F., Michaud, H., Tarte, K., Teissier, N., Favier, B., Roussel, M., et al. (2023) · The Journal of Experimental Medicine · doi:10.1084/jem.20230002 · Cited by 11

Fate-Mapping Macrophages: From Ontogeny to Functions

Ahlback, A., & Gentek, R. (2023) · Methods in molecular biology · doi:10.1007/978-1-0716-3437-0_2 · Cited by 13

Red Light Modulates Ultraviolet-Induced Gene Expression in the Epidermis of Hairless Mice

Myakishev-Rempel, M., Stadler, I., Polesskaya, O., et al. (2015) · Photomedicine and Laser Surgery · doi:10.1089/pho.2015.3916 · Cited by 11

Isolation and Identification of Murine Serous Cavity Macrophages

Bain, C. C., & Jenkins, S. J. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-7837-3_5 · Cited by 12

Antibody-Mediated Protection against Staphylococcus aureus Dermonecrosis: Synergy of Toxin Neutralization and Neutrophil Recruitment

Yang, C. W., Ruiz‐Rosado, J. D. D., Robledo-Avila, F. H., et al. (2020) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2020.09.001 · Cited by 11

Inhibition of effector antigen-specific T cells by intradermal administration of heme oxygenase-1 inducers

Simon, T., Pogu, J., Remy, S., Brau, F., Pogu, S., Maquigneau, M., Fonteneau, J., Poirier, N., Vanhove, B., Blancho, G., et al. (2017) · Journal of Autoimmunity · doi:10.1016/j.jaut.2017.03.005 · Cited by 11

Classification of Wounds and the Physiology of Wound Healing

Gupta, A. (2021) · Springer eBooks · doi:10.1007/978-981-16-2677-7_1 · Cited by 13

Isolation of Human Skin Dendritic Cell Subsets

Gunawan, M., Jardine, L., & Haniffa, M. A. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-3606-9_8 · Cited by 10

Dermal macrophage and its potential in inducing hair follicle regeneration

Gao, Y., Wang, J., Zhu, D., Miao, Y., & Hu, Z. (2021) · Molecular Immunology · doi:10.1016/j.molimm.2021.02.021 · Cited by 12

Skin as an immune organ and the site of biomimetic, non-invasive vaccination

Chopra, A., & Gupta, A. (2022) · Medicine in Novel Technology and Devices · doi:10.1016/j.medntd.2022.100196 · Cited by 10

Fascia Promotes Adipose Tissue Regeneration by Improving Early Macrophage Infiltration after Fat Grafting in a Mouse Model

Bi, X., Li, B., Zou, J., Zhao, J., Chen, Y., Wang, X., Lu, F., Li, Y., Dong, Z., & Gao, J. (2023) · Plastic & Reconstructive Surgery · doi:10.1097/prs.0000000000010259 · Cited by 10

A Matter of Perspective: Moving from a Pre-omic to a Systems-Biology Vantage of Monocyte-Derived Cell Function and Nomenclature

Guilliams, M., & MALISSEN, B. (2016) · Immunity · doi:10.1016/j.immuni.2015.12.020 · Cited by 10

Monitoring Skin Dendritic Cells in Steady State and Inflammation by Immunofluorescence Microscopy and Flow Cytometry

Ober-Blöbaum, J. L., Ortner, D., Haid, B., et al. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-6786-5_3 · Cited by 10

IL-1R Type 1–Deficient Mice Demonstrate an Impaired Host Immune Response against Cutaneous Vaccinia Virus Infection

Tian, T., Jin, M. Q., Dubin, K. A., King, S. L., Hoetzenecker, W., Murphy, G. F., Chen, C. A., Kupper, T. S., & Fuhlbrigge, R. C. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1500106 · Cited by 10

Analysis of Inflammatory and Homeostatic Roles of Tissue-resident Macrophages in the Progression of Cholesteatoma by RNA-Seq

Fang, L., Chen, L., Bi, L., et al. (2020) · Immunological Investigations · doi:10.1080/08820139.2020.1781161 · Cited by 10

Signaling pathways that control mRNA translation initiation in macrophages

Tabatabaei, N., Hou, S., Kim, K.-W., & Tahmasebi, S. (2020) · Cellular Signalling · doi:10.1016/j.cellsig.2020.109700 · Cited by 10

Illuminating the covert mission of mononuclear phagocytes in their regional niches

Chong, S. Z., Evrard, M., Goh, C. C., & Ng, L. G. (2017) · Current Opinion in Immunology · doi:10.1016/j.coi.2017.12.004 · Cited by 10

Molecular control of tissue-resident macrophage identity by nuclear receptors

Porcuna, J., Menéndez-Gutierrez, M. P., & Ricote, M. (2020) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2020.04.001 · Cited by 10

Monocytes give rise to Langerhans cells that preferentially migrate to lymph nodes at steady state

Raquer-McKay, H. M., Maqueda‐Alfaro, R. A., Saravanan, S., Hornero, R. A., Clausen, B. E., Gottfried‐Blackmore, A., & Idoyaga, J. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2404927121 · Cited by 8

Regulatory T Cells but Not IL-10 Impair Cell-Mediated Immunity in Human Papillomavirus E7+ Hyperplastic Epithelium

Bashaw, A. A., Zhou, C., Yu, M., Tolley, L. K., Leggatt, G. R., Frazer, I. H., & Chandra, J. (2020) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2020.10.011 · Cited by 9

Macrophages and dendritic cells

Sutton, K., Balic, A., Kaspers, B., & Vervelde, L. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-818708-1.00003-8 · Cited by 9

Lupus-prone NZM2328 mice exhibit enhanced UV-induced myeloid cell recruitment and activation in a type I interferon dependent manner

Maz, M. P., Reddy, A. L., Berthier, C. C., Tsoi, L. C., Colesa, D. J., Wolf, S., Shi, H., Loftus, S. N., Moallemian, R., Wasikowski, R., et al. (2024) · Journal of Autoimmunity · doi:10.1016/j.jaut.2024.103296 · Cited by 8

Arc/Arg3.1 defines dendritic cells and Langerhans cells with superior migratory ability independent of phenotype and ontogeny in mice

Tintelnot, J., Ufer, F., Engler, J. B., Winkler, H., Lücke, K., Mittrücker, H., & Friese, M. A. (2019) · European Journal of Immunology · doi:10.1002/eji.201847797 · Cited by 7

Psychoneurobiomodulation: an emerging concept to understand the systemic effects of neurophysiological acupuncture

Quiróz-González, S., Toro, A. O., Piceno, Y. G., et al. (2019) · Longhua Chinese Medicine · doi:10.21037/lcm.2019.12.01 · Cited by 8

TLR2 Dimerization Blockade Allows Generation of Homeostatic Intestinal Macrophages under Acute Colitis Challenge

Gross-Vered, M., Shmuel-Galia, L., Zarmi, B., Humphries, F., Thaiss, C. A., Salame, T., David, E., Chappell‐Maor, L., Fitzgerald, K. A., Shai, Y., et al. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1900470 · Cited by 8

Cluster of differentiation frequency on antigen presenting-cells: The next step to cervical cancer prognosis?

Aghbash, P. S., Shirvaliloo, M., Kasho, A. K. A., Alinezhad, F., Nauwynck, H., & Baghi, H. B. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.108896 · Cited by 8

Migrating Lung Monocytes Internalize and Inhibit Growth of Aspergillus fumigatus Conidia

Schiefermeier-Mach, N., Haller, T., Geley, S., & Perkhofer, S. (2020) · Pathogens · doi:10.3390/pathogens9120983 · Cited by 8

The Unfolded Protein Response in the Immune Cell Development: Putting the Caretaker in the Driving Seat

Tavernier, S. J., Lambrecht, B. N., & Janssens, S. (2017) · Current topics in microbiology and immunology · doi:10.1007/82_2017_1 · Cited by 6

The role of macrophage migratory behavior in development, homeostasis and tumor invasion

Murrey, M. W., Ng, I. T., & Pixley, F. J. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1480084 · Cited by 8

Genetic Modification of Primary Human Myeloid Cells to Study Cell Migration, Activation, and Organelle Dynamics

Greiner, D., Scott, T. M., Olson, G. S., Aderem, A. A., Roh‐Johnson, M., & Johnson, J. S. (2022) · Current Protocols · doi:10.1002/cpz1.514 · Cited by 7

The Phenotypic Characterization of the Human Renal Mononuclear Phagocytes Reveal a Co-Ordinated Response to Injury

Leone, D. A., Kozakowski, N., Kornauth, C., Waidacher, T., Neudert, B., Loeffler, A. G., Haitel, A., Rees, A. J., & Kain, R. (2016) · PLoS ONE · doi:10.1371/journal.pone.0151674 · Cited by 7

Tissue imprinting defines functional mosaic of dermal macrophagesPreprint

Lohrmann, F., Sankowski, R., Schwer, S., Neuber, J., Vlachou, E. P., Westermann, F., Troesch, E., Kolter, J., Loesslein, A. K., Mahapatra, K. D., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.09.631670 · Cited by 7

Heterogeneity of myeloid cells in common cancers: Single cell insights and targeting strategies

Jing, Z.-Q., Luo, Z.-Q., Chen, S.-R., & Sun, Z. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.112253 · Cited by 7

Apoptosis and Cell Clearance in Skin Wound Healing

Cleene, H. K. L. D., Keçeli, B. N., & Maschalidi, S. (2025) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-92785-0_5 · Cited by 6

Characterization of the immune landscape in healthy mouse prostate and during prostate cancer progression

Pervizou, D., Chiara, J. D., Spinelli, L., NESTOR-MARTIN, M., Chasson, L., LEN-TAYON, K., Yanushko, D., FIORE, F., Bajénoff, M., Malissen, B., et al. (2025) · OncoImmunology · doi:10.1080/2162402x.2025.2562220 · Cited by 6

Skin immunity and inflammation: cellular interactions and communication

Narayanan, D., Sim, S.-L., & Kumari, S. (2025) · Clinical & Translational Immunology · doi:10.1002/cti2.70053 · Cited by 10

PDGFRα‐lineage origin directs monocytes to trafficking proficiency to support peripheral immunity

Li, Y., Yamazaki, S., Takaki, E., Ouchi, Y., Kitayama, T., & Tamai, K. (2021) · European Journal of Immunology · doi:10.1002/eji.202149479 · Cited by 7

Downregulation of MHC Class II by Ubiquitination Is Required for the Migration of CD206+ Dendritic Cells to Skin-Draining Lymph Nodes

Majdoubi, A., Lee, J. S., Balood, M., Sabourin, A., DeMontigny, A., Kishta, O. A., Moulefera, M. A., Galbas, T., Yun, T. J., Talbot, S., et al. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1900593 · Cited by 6

Intermediate monocytes correlate with CXCR3+ Th17 cells but not with bone characteristics in untreated early rheumatoid arthritis

Drevinge, C., Scheffler, J. M., Koro-Arvidsson, C., Sundh, D., Carlsten, H., Gjertsson, I., Lindholm, C., Lorentzon, M., Rudin, A., Ekwall, A. H., et al. (2021) · PLoS ONE · doi:10.1371/journal.pone.0249205 · Cited by 6

Multi-Tissue Characterization of GILZ Expression in Dendritic Cell Subsets at Steady State and in Inflammatory Contexts

Docq, M., Vétillard, M., Gallego, C., Jaracz‐Ros, A., Mercier‐Nomé, F., Bachelerie, F., & Schlecht‐Louf, G. (2021) · Cells · doi:10.3390/cells10113153 · Cited by 6

Tissue‐specific antigen‐presenting cells contribute to distinct phenotypes of allergy

Schülke, S., Gilles, S., Jirmo, A. C., & Mayer, J. U. (2023) · European Journal of Immunology · doi:10.1002/eji.202249980 · Cited by 6

Tumor eradication by hetIL-15 locoregional therapy correlates with an induced intratumoral CD103intCD11b+ dendritic cell population

Stellas, D., Karaliota, S., Stravokefalou, V., Angel, M., Nagy, B. A., Goldfarbmuren, K. C., Bergamaschi, C., Felber, B. K., & Pavlakis, G. N. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112501 · Cited by 8

Interactions between macrophage membrane and lipid mediators during cardiovascular diseases with the implications of scavenger receptors

Ravi, S., Martin, L. C., Krishnan, M., Kumaresan, M., Manikandan, B., & Ramar, M. (2023) · Chemistry and Physics of Lipids · doi:10.1016/j.chemphyslip.2023.105362 · Cited by 6

The Effects of IL-22 on the Inflammatory Mediator Production, Proliferation, and Barrier Function of HUVECs

He, X., Li, H., Chen, Y., et al. (2016) · Inflammation · doi:10.1007/s10753-016-0341-3 · Cited by 6

Role of Dendritic Cells in Pathogen Infections: A Current Perspective

Muñoz‐Carrillo, J. L., Contreras‐Cordero, J. F., Gutiérrez‐Coronado, O., Villalobos‐Gutiérrez, P. T., Ramos-Gracia, L. G., & Vargas‐Barboza, J. M. (2021) · IntechOpen eBooks · doi:10.5772/intechopen.95551 · Cited by 6

Innate Immunity and Inflammation

McKarns, S. C. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.64228-9 · Cited by 6

Myeloid Cells and Chronic Liver Disease: a Comprehensive Review

Lian, M., Selmi, C. F., Gershwin, M. E., & Ma, X. (2018) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-017-8664-x · Cited by 6

Poised cell circuits in human skin are activated in diseasePreprint

Reynolds, G., Végh, P., Fletcher, J., Poyner, E. F. M., Stephenson, E., Goh, I., Botting, R. A., Huang, N., Olabi, B., Dubois, A., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.11.05.369363 · Cited by 7

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Hanlon, M. M., Fearon, U., & Gravallese, E. M. (2026) · European Journal of Immunology · doi:10.1002/eji.70124 · Cited by 8

Protocol for isolation and spectral flow cytometry analysis of immune cells from the murine exocrine and endocrine pancreas

Steiger, L., Baumann, Z., Keller, L., et al. (2023) · STAR Protocols · doi:10.1016/j.xpro.2023.102664 · Cited by 5

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Wemyss, K., & Konkel, J. E. (2022) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2022.106194 · Cited by 5

Macrophage Development and Function

Makdissi, N. (2023) · Methods in molecular biology · doi:10.1007/978-1-0716-3437-0_1 · Cited by 5

Molecular and cellular pruritus mechanisms in the host skin

Li, L., Li, Z.-E., Mo, Y.-L., Li, W.-Y., Li, H., Yan, G., Qin, X., & Piao, L. (2024) · Experimental and Molecular Pathology · doi:10.1016/j.yexmp.2024.104889 · Cited by 7

Myeloid cells pave the way for lymphatic system development and maintenance

Ivanov, S., & Randolph, G. J. (2017) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-017-1951-9 · Cited by 5

Interactions neuro-immunes dans la peau

Debroas, G., Hoeffel, G., Reynders, A., & Ugolini, S. (2018) · médecine/sciences · doi:10.1051/medsci/20183405016 · Cited by 7

Optimized protocol for the preparation of single cells from cutaneous wounds for flow cytometric cell sorting and analysis of macrophages

Shakya, S., Asosingh, K., Mack, J. A., & Maytin, E. V. (2020) · MethodsX · doi:10.1016/j.mex.2020.101027 · Cited by 5

Non‐zero‐sum microbiome immune system interactions

Tuganbaev, T., & Honda, K. (2021) · European Journal of Immunology · doi:10.1002/eji.202049065 · Cited by 7

Developmental programming of macrophages by early life adversity

Pinto, M. M., Potter, H. G., Ahlback, A., & Gentek, R. (2022) · International review of cytology · doi:10.1016/bs.ircmb.2022.02.003 · Cited by 5

Loss of T cell tolerance in the skin following immunopathology is linked to failed restoration of the dermal niche by recruited macrophages

West, H. C., Davies, J., Henderson, S. R., Adegun, O. K., Ward, S., Ferrer, I. R., Tye, C. A., Vallejo, A. F., Jardine, L., Collin, M. P., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110819 · Cited by 5

Phagocyte Development

Patel, A. A., & Yona, S. (2018) · Wiley eBooks · doi:10.1002/9780470015902.a0001218.pub2 · Cited by 6

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Lai, G., Zhao, X., Chen, Y., Xie, T., Su, Z., Lin, J., Chen, K., & Chen, K. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.114260 · Cited by 5

Commensal-myeloid crosstalk in neonatal skin regulates interleukin-1 signaling and cutaneous type 17 inflammation

Dhariwala, M. O., Carale, R. O., DeRogatis, A. M., Rodriguez-Valbuena, H., Okoro, J. N., Ekstrand, C. A., Weckel, A., Tran, V. M., Habrylo, I., Barrere‐Cain, R., et al. (2026) · Immunity · doi:10.1016/j.immuni.2026.01.005 · Cited by 8

Transcription factor Etv3 controls the tolerogenic function of dendritic cells

Adams, N. M., Martinez-Krams, D., Esteva, E., Ra, A. C., Alexiou, A. I., Jin, H., Yun, T. J., Tellaoui, R. S., Mudianto, T., Vollmer, E., et al. (2026) · Science · doi:10.1126/science.ads1246 · Cited by 7

Trained immunity in skin infections: Macrophages and beyond

Gres, V., Göcer, M., Kolter, J., & Henneke, P. (2025) · eLife · doi:10.7554/elife.106688 · Cited by 7

Obesity alters the macrophages’ response to Leishmania major in C57BL/6 mice

Martins, V. D., Vaz, L. G., Barbosa, S. C., Paixão, P. H. D. M., Torres, L., de Oliveira, M. F. A., Oliveira, M. D. A., Vieira, L. Q., Faria, A. M. C., & Maioli, T. U. (2024) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiae171 · Cited by 4

The helper function of monocytes from aged humans in lymphocyte activation by mitogens.

Tsujimoto, M., Tsuda, T., Kiichiro, O. T. A., et al. (1985) · Nippon Ronen Igakkai Zasshi Japanese Journal of Geriatrics · doi:10.3143/geriatrics.22.450

Correlation between Entothelial Microparticle Binding to Monocytes and Monocyte Nitric Oxide Production in Prothrombotic and Inflammatory Disorders.

Chirinos, J. A., Jy, W., Carpio, F. D., et al. (2005) · Blood · doi:10.1182/blood.v106.11.3860.3860

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Chow, S., Ou, H., Sheu, W. H., Wang, J., & Chen, Y.-W. (2005) · Thrombosis and Haemostasis · doi:10.1160/th05-02-0139 · Cited by 16

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Kamińska, J., Lisowska, A., Koper‐Lenkiewicz, O. M., et al. (2019) · The American Journal of the Medical Sciences · doi:10.1016/j.amjms.2019.02.010 · Cited by 9

724 Effects of Oxidized LDL on Monocyte Trans-endothelial Migration

Hashimoto, K., Kataoka, N., NAKAMURA, E., et al. (2006) · The proceedings of the JSME annual meeting · doi:10.1299/jsmemecjo.2006.5.0_247