Antimicrobials from human skin commensal bacteria protect against Staphylococcus aureus and are deficient in atopic dermatitis

QIIME allows analysis of high-throughput community sequencing data

Caporaso, J. G., Kuczynski, J., Stombaugh, J., Bittinger, K., Bushman, F. D., Costello, E. K., Fierer, N., Peña, A. G., Goodrich, J. K., Gordon, J. I., et al. (2010) · Nature Methods · doi:10.1038/nmeth.f.303 · Cited by 34,887 · see citing works

Search and clustering orders of magnitude faster than BLAST

Edgar, R. C. (2010) · Bioinformatics · doi:10.1093/bioinformatics/btq461 · Cited by 20,617 · see citing works

Naive Bayesian Classifier for Rapid Assignment of rRNA Sequences into the New Bacterial Taxonomy

Wang, Q., Garrity, G. M., Tiedje, J. M., & Cole, J. R. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.00062-07 · Cited by 19,770 · see citing works

UCHIME improves sensitivity and speed of chimera detection

Edgar, R. C., Haas, B. J., Clemente, J. C., Quince, C., & Knight, R. (2011) · Bioinformatics · doi:10.1093/bioinformatics/btr381 · Cited by 15,114 · see citing works

Greengenes, a Chimera-Checked 16S rRNA Gene Database and Workbench Compatible with ARB

DeSantis, T. Z., Hugenholtz, P., Larsen, N., Rojas, M., Brodie, E. L., Keller, K., Huber, T., Dalevi, D., Hu, P., & Andersen, G. L. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.03006-05 · Cited by 10,891 · see citing works

Ribosomal Database Project: data and tools for high throughput rRNA analysis

Cole, J. R., Wang, Q., Fish, J. A., Chai, B., McGarrell, D. M., Sun, Y., Brown, C. T., Porras‐Alfaro, A., Kuske, C. R., & Tiedje, J. M. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt1244 · Cited by 4,322 · see citing works

Atopic Dermatitis: Global Epidemiology and Risk Factors

Nutten, S. (2015) · Annals of Nutrition and Metabolism · doi:10.1159/000370220 · Cited by 3,077 · see citing works

Topographical and Temporal Diversity of the Human Skin Microbiome

Grice, E. A., Kong, H. H., Conlan, S., Deming, C. B., Davis, J., Young, A. C., Program, N. C. S., Bouffard, G. G., Blakesley, R. W., Murray, P. R., et al. (2009) · Science · doi:10.1126/science.1171700 · Cited by 2,953 · see citing works

Differential abundance analysis for microbial marker-gene surveys

Paulson, J. N., Stine, O. C., Bravo, H. C., & Pop, M. (2013) · Nature Methods · doi:10.1038/nmeth.2658 · Cited by 2,437 · see citing works

antiSMASH: rapid identification, annotation and analysis of secondary metabolite biosynthesis gene clusters in bacterial and fungal genome sequences

Medema, M. H., Blin, K., Cimermančič, P., de Jager, V., Zakrzewski, P., Fischbach, M. A., Weber, T., Eriko Takano, A., & Rainer Breitling, A. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr466 · Cited by 2,013 · see citing works

Endogenous Antimicrobial Peptides and Skin Infections in Atopic Dermatitis

Ong, P. Y., Ohtake, T., Brandt, C., Strickland, I., Boguniewicz, M., Ganz, T., Gallo, R. L., & Leung, D. Y. M. (2002) · New England Journal of Medicine · doi:10.1056/nejmoa021481 · Cited by 1,960 · see citing works

Plasmacytoid dendritic cells sense self-DNA coupled with antimicrobial peptide

Lande, R., Gregorio, J., Facchinetti, V., Chatterjee, B., Wang, Y.-H., Homey, B., Cao, W., Wang, Y.-H., Su, B., Nestle, F. O., et al. (2007) · Nature · doi:10.1038/nature06116 · Cited by 1,910 · see citing works

Temporal shifts in the skin microbiome associated with disease flares and treatment in children with atopic dermatitis

Kong, H. H., Oh, J., Deming, C., Conlan, S., Grice, E. A., Beatson, M. A., Nomicos, E., Polley, E. C., Komarow, H. D., Program, N. C. S., et al. (2012) · Genome Research · doi:10.1101/gr.131029.111 · Cited by 1,808 · see citing works

An improved dual-indexing approach for multiplexed 16S rRNA gene sequencing on the Illumina MiSeq platform

Fadrosh, D. W., Ma, B., Gajer, P., Sengamalay, N., Ott, S., Brotman, R. M., & Ravel, J. (2014) · Microbiome · doi:10.1186/2049-2618-2-6 · Cited by 1,698 · see citing works

Surfactant Protein-A Binds Group B Streptococcus Enhancing Phagocytosis and Clearance from Lungs of Surfactant Protein-A–Deficient Mice

LeVine, A. M., Kurak, K. E., Wright, J. R., Watford, W. T., Bruno, M. D., Ross, G. F., Whitsett, J. A., & Korfhagen, T. R. (1999) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/ajrcmb.20.2.3303 · Cited by 1,272 · see citing works

Innate antimicrobial peptide protects the skin from invasive bacterial infection

Nizet, V., Ohtake, T., Lauth, X., Trowbridge, J., Rudisill, J., Dorschner, R. A., Pestonjamasp, V., Piraino, J., Huttner, K., & Gallo, R. L. (2001) · Nature · doi:10.1038/35106587 · Cited by 1,198 · see citing works

Biogeography and individuality shape function in the human skin metagenome

Program, N. C. S., Oh, J., Byrd, A. L., Deming, C., Conlan, S., Kong, H. H., & Segre, J. A. (2014) · Nature · doi:10.1038/nature13786 · Cited by 1,148 · see citing works

Compartmentalized Control of Skin Immunity by Resident Commensals

Naik, S., Bouladoux, N., Wilhelm, C., Molloy, M. J., Salcedo, R., Kastenmuller, W., Deming, C., Quinones, M., Koo, L., Conlan, S., et al. (2012) · Science · doi:10.1126/science.1225152 · Cited by 1,092 · see citing works

Staphylococcus epidermidis Esp inhibits Staphylococcus aureus biofilm formation and nasal colonization

Iwase, T., Uehara, Y., Shinji, H., Tajima, A., Seo, H., Takada, K., Agata, T., & Mizunoe, Y. (2010) · Nature · doi:10.1038/nature09074 · Cited by 991 · see citing works

Epithelial antimicrobial defence of the skin and intestine

Gallo, R. L., & Hooper, L. V. (2012) · Nature reviews. Immunology · doi:10.1038/nri3228 · Cited by 959 · see citing works

Staphylococcus aureus in the lesions of atopic dermatitis

LEYDEN, J. J., MARPLES, R. R., & Kligman, A. M. (1974) · British Journal of Dermatology · doi:10.1111/j.1365-2133.1974.tb06447.x · Cited by 894 · see citing works

Commensal–dendritic-cell interaction specifies a unique protective skin immune signature

Naik, S., Bouladoux, N., Linehan, J. L., Han, S.-J., Harrison, O. J., Wilhelm, C., Conlan, S., Himmelfarb, S., Byrd, A. L., Deming, C., et al. (2015) · Nature · doi:10.1038/nature14052 · Cited by 820 · see citing works

Thymic stromal lymphopoietin is released by human epithelial cells in response to microbes, trauma, or inflammation and potently activates mast cells

Allakhverdi, Z., Comeau, M. R., Jessup, H. K., Yoon, B. P., Brewer, A. W., Chartier, S., Paquette, N., Ziegler, S. F., Sarfati, M., & Delespesse, G. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20062211 · Cited by 787 · see citing works

Commensal bacteria regulate Toll-like receptor 3–dependent inflammation after skin injury

Lai, Y., Di Nardo, A., Nakatsuji, T., Leichtle, A., Yang, Y., Cogen, A. L., Wu, Z.-R., Hooper, L. V., Schmidt, R. R., von Aulock, S., et al. (2009) · Nature Medicine · doi:10.1038/nm.2062 · Cited by 781 · see citing works

Paneth Cells: Maestros of the Small Intestinal Crypts

Clevers, H. C., & Bevins, C. L. (2013) · Annual Review of Physiology · doi:10.1146/annurev-physiol-030212-183744 · Cited by 698 · see citing works

Lantibiotics: structure, biosynthesis and mode of action

McAuliffe, O. E., Ross, R. P., & Hill, C. (2001) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2001.tb00579.x · Cited by 682 · see citing works

Staphylococcus δ-toxin induces allergic skin disease by activating mast cells

Nakamura, Y., Oscherwitz, J., Cease, K. B., Chan, S. M., Muñoz-Planillo, R., Hasegawa, M., Villaruz, A. E., Cheung, G. Y. C., McGavin, M. J., Travers, J. B., et al. (2013) · Nature · doi:10.1038/nature12655 · Cited by 558 · see citing works

Degradation of Human Antimicrobial Peptide LL-37 by Staphylococcus aureus -Derived Proteinases

Sieprawska‐Lupa, M., Mydel, P. M., Krawczyk, K., Wójcik, K., Puklo, M., Lupa, B., Suder, P., Silberring, J., Reed, M. S., Pohl, J., et al. (2004) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.48.12.4673-4679.2004 · Cited by 552 · see citing works

Dysbiosis and Staphylococcus aureus Colonization Drives Inflammation in Atopic Dermatitis

Kobayashi, T., Glatz, M., Horiuchi, K., Kawasaki, H., Akiyama, H., Kaplan, D. H., Kong, H. H., Amagai, M., & Nagao, K. (2015) · Immunity · doi:10.1016/j.immuni.2015.03.014 · Cited by 549 · see citing works

Structure and function of the human skin microbiome

Schommer, N. N., & Gallo, R. L. (2013) · Trends in Microbiology · doi:10.1016/j.tim.2013.10.001 · Cited by 542 · see citing works

Dermal adipocytes protect against invasive <i>Staphylococcus aureus</i> skin infection

Zhang, L.-J., Guerrero-Juarez, C. F., Hata, T., Bapat, S. P., Ramos, R., Plikus, M. V., & Gallo, R. L. (2015) · Science · doi:10.1126/science.1260972 · Cited by 471 · see citing works

Bacteriocin production augments niche competition by enterococci in the mammalian gastrointestinal tract

Kommineni, S., Bretl, D. J., Lam, V., Chakraborty, R., Hayward, M., Simpson, P., Cao, Y., Bousounis, P., Kristich, C. J., & Salzman, N. H. (2015) · Nature · doi:10.1038/nature15524 · Cited by 458 · see citing works

Microbial Diversity in Water and Sediment of Lake Chaka, an Athalassohaline Lake in Northwestern China

Jiang, H., Dong, H., Zhang, G., Yu, B., Chapman, L. R., & Fields, M. W. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.02869-05 · Cited by 449 · see citing works

Activation of TLR2 by a Small Molecule Produced by Staphylococcus epidermidis Increases Antimicrobial Defense against Bacterial Skin Infections

Lai, Y., Cogen, A. L., Radek, K. A., Park, H. J., MacLeod, D. T., Leichtle, A., Ryan, A. F., Di Nardo, A., & Gallo, R. L. (2010) · Journal of Investigative Dermatology · doi:10.1038/jid.2010.123 · Cited by 446 · see citing works

Selective Antimicrobial Action Is Provided by Phenol-Soluble Modulins Derived from Staphylococcus epidermidis, a Normal Resident of the Skin

Cogen, A. L., Yamasaki, K., Sanchez, K. M., Dorschner, R. A., Lai, Y., MacLeod, D. T., Torpey, J. W., Otto, M., Nizet, V., Kim, J. E., et al. (2010) · Journal of Investigative Dermatology · doi:10.1038/jid.2009.243 · Cited by 432 · see citing works

Immunity against Staphylococcus aureus cutaneous infections

Miller, L. S., & Cho, J. S. (2011) · Nature reviews. Immunology · doi:10.1038/nri3010 · Cited by 428 · see citing works

Antimicrobial Peptides: Old Molecules with New Ideas

Nakatsuji, T., & Gallo, R. L. (2011) · Journal of Investigative Dermatology · doi:10.1038/jid.2011.387 · Cited by 397 · see citing works

Microbial Symbiosis with the Innate Immune Defense System of the Skin

Gallo, R. L., & Nakatsuji, T. (2011) · Journal of Investigative Dermatology · doi:10.1038/jid.2011.182 · Cited by 387 · see citing works

Staphylococcus aureus Exploits Epidermal Barrier Defects in Atopic Dermatitis to Trigger Cytokine Expression

Nakatsuji, T., Chen, T. H., Two, A. M., Chun, K., Narala, S., Geha, R. S., Hata, T. R., & Gallo, R. L. (2016) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2016.05.127 · Cited by 365 · see citing works

A mass spectrometry–guided genome mining approach for natural product peptidogenomics

Kersten, R. D., Yang, Y., Xu, Y., Cimermančič, P., Nam, S.-J., Fenical, W., Fischbach, M. A., Moore, B. S., & Dorrestein, P. C. (2011) · Nature Chemical Biology · doi:10.1038/nchembio.684 · Cited by 360 · see citing works

Molecular cartography of the human skin surface in 3D

Bouslimani, A., Porto, C., Rath, C. M. B., Wang, M., Guo, Y., González, A., Berg-Lyons, D., Ackermann, G. L., Christensen, G. J. M., Nakatsuji, T., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1424409112 · Cited by 353 · see citing works

Cytokine Milieu of Atopic Dermatitis Skin Subverts the Innate Immune Response to Vaccinia Virus

Howell, M. D., Gallo, R. L., Boguniewicz, M., Jones, J. F., Wong, C., Streib, J. E., & Leung, D. Y. M. (2006) · Immunity · doi:10.1016/j.immuni.2006.02.006 · Cited by 335 · see citing works

Skin Commensals Amplify the Innate Immune Response to Pathogens by Activation of Distinct Signaling Pathways

Wanke, I., Steffen, H., Christ, C., Krismer, B., Götz, F., Peschel, A., Schaller, M., & Schittek, B. (2010) · Journal of Investigative Dermatology · doi:10.1038/jid.2010.328 · Cited by 284 · see citing works

Catalytic promiscuity in the biosynthesis of cyclic peptide secondary metabolites in planktonic marine cyanobacteria

Ли, Б., Sher, D., Kelly, L., Shi, Y., Huang, K. H., Knerr, P. J., Joewono, I., Rusch, D. B., Chisholm, S. W., & van der Donk, W. A. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0913677107 · Cited by 272 · see citing works

Establishment of an Analytical System for the Human Fecal Microbiota, Based on Reverse Transcription-Quantitative PCR Targeting of Multicopy rRNA Molecules

Matsuda, K., Tsuji, H., Asahara, T., Matsumoto, K., Takada, T., & Nomoto, K. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.01843-08 · Cited by 262 · see citing works

Antimicrobial and protease inhibitory functions of the human cathelicidin (hCAP18/LL-37) prosequence

Zaiou, M., Nizet, V., & Gallo, R. L. (2003) · Journal of Investigative Dermatology · doi:10.1046/j.1523-1747.2003.12132.x · Cited by 256 · see citing works

Staphylococcus epidermidis Antimicrobial δ-Toxin (Phenol-Soluble Modulin-γ) Cooperates with Host Antimicrobial Peptides to Kill Group A Streptococcus

Cogen, A. L., Yamasaki, K., Muto, J., Sanchez, K. M., Crotty Alexander, L., Tanios, J., Lai, Y., Kim, J. E., Nizet, V., & Gallo, R. L. (2010) · PLoS ONE · doi:10.1371/journal.pone.0008557 · Cited by 245 · see citing works

Mechanism of HBD-3 deficiency in atopic dermatitis

Howell, M. D., Boguniewicz, M., Pastore, S., Novak, N., Bieber, T., Girolomoni, G., & Leung, D. Y. M. (2006) · Clinical Immunology · doi:10.1016/j.clim.2006.08.008 · Cited by 208 · see citing works

Enteric Microbiome Metabolites Correlate with Response to Simvastatin Treatment

Kaddurah-Daouk, R., Baillie, R. A., Zhu, H., Zeng, Z.-B., Wiest, M. M., Nguyen, U. T., Wojnoonski, K., Watkins, S. M., Trupp, M., & Krauss, R. M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025482 · Cited by 193 · see citing works

Staphylococcus aureus membrane and diacylated lipopeptide induce thymic stromal lymphopoietin in keratinocytes through the Toll-like receptor 2–Toll-like receptor 6 pathway

Vu, A. T., Baba, T., Chen, X., Lê, T. A., Kinoshita, H., Xie, Y., Kamijo, S., Hiramatsu, K., Ikeda, S., Ogawa, H., et al. (2010) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2010.09.002 · Cited by 186 · see citing works

Transplantation of human skin microbiota in models of atopic dermatitis

Myles, I. A., Williams, K. W., Reckhow, J. D., Jammeh, M. L., Pincus, N. B., Sastalla, I., Saleem, D., Stone, K. D., & Datta, S. K. (2016) · JCI Insight · doi:10.1172/jci.insight.86955 · Cited by 180 · see citing works

Vitamin B 12 modulates the transcriptome of the skin microbiota in acne pathogenesis

Kang, D., Shi, B., Erfe, M. C. B., Craft, N. A., & Li, H. (2015) · Science Translational Medicine · doi:10.1126/scitranslmed.aab2009 · Cited by 172 · see citing works

Neonatal Skin in Mice and Humans Expresses Increased Levels of Antimicrobial Peptides: Innate Immunity During Development of the Adaptive Response

Dorschner, R. A., Lin, K. H., Murakami, M., & Gallo, R. L. (2003) · Pediatric Research · doi:10.1203/01.pdr.0000057205.64451.b7 · Cited by 149 · see citing works

Antimicrobial and antifungal activities of a novel cationic antimicrobial peptide, omiganan, in experimental skin colonisation models

Rubinchik, E., Dugourd, D., de Algara, T. R., Pasetka, C., & Friedland, H. D. (2009) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2009.05.003 · Cited by 120 · see citing works

Evaluating the Impact of Different Sequence Databases on Metaproteome Analysis: Insights from a Lab-Assembled Microbial Mixture

Tanca, A., Palomba, A., Deligios, M., Cubeddu, T., Fraumene, C., Biosa, G., Pagnozzi, D., Addis, M. F., & Uzzau, S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0082981 · Cited by 118 · see citing works

A Novel Lipopeptide from Skin Commensal Activates TLR2/CD36-p38 MAPK Signaling to Increase Antibacterial Defense against Bacterial Infection

Li, D., Lei, H., Li, Z., Li, H., Wang, Y., & Lai, Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0058288 · Cited by 105 · see citing works

Effects of the Staphylococcus aureus and Staphylococcus epidermidis Secretomes Isolated from the Skin Microbiota of Atopic Children on CD4+ T Cell Activation

Laborel-Préneron, E., Bianchi, P., Boralévi, F., Lehours, P., Fraysse, F., Morice‐Picard, F., Sugai, M., Sato’o, Y., Badiou, C., Lina, G., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0141067 · Cited by 101 · see citing works

Direct Detection of Staphylococcus aureus from Adult and Neonate Nasal Swab Specimens Using Real-Time Polymerase Chain Reaction

Paule, S. M., Pasquariello, A. C., Hacek, D. M., Fisher, A. G., Thomson, R. B., Kaul, K. L., & Peterson, L. R. (2004) · Journal of Molecular Diagnostics · doi:10.1016/s1525-1578(10)60509-0 · Cited by 90 · see citing works

History of eczema herpeticum is associated with the inability to induce human β-defensin (HBD)-2, HBD-3 and cathelicidin in the skin of patients with atopic dermatitis

Hata, T., Kotol, P. F., Boguniewicz, M., Taylor, P. A., Paik, A. J., Jackson, M., Nguyen, M., Kabigting, F. D., Miller, J., Gerber, M., et al. (2010) · British Journal of Dermatology · doi:10.1111/j.1365-2133.2010.09892.x · Cited by 87 · see citing works

Injury downregulates the expression of the human cathelicidin protein hCAP18/LL‐37 in atopic dermatitis

Mallbris, L., Carlén, L. M., Wei, T., Heilborn, J. D., Nilsson, M. F., Granath, F., & Ståhle, M. (2009) · Experimental Dermatology · doi:10.1111/j.1600-0625.2009.00918.x · Cited by 65 · see citing works

Bacteriocins Pep5 and Epidermin Inhibit Staphylococcus epidermidis Adhesion to Catheters

Fontana, M. B. C., Bastos, M. D. C. D. F., & Brandelli, A. (2006) · Current Microbiology · doi:10.1007/s00284-005-0152-5 · Cited by 56 · see citing works

Whole-Genome Sequence of Staphylococcus hominis, an Opportunistic Pathogen

Jiang, S., Zheng, B., Ding, W., Lv, L., Ji, J., Zhang, H., Xiao, Y., & Li, L. (2012) · Journal of Bacteriology · doi:10.1128/jb.00991-12 · Cited by 32 · see citing works

EGG YOLK AGAR FOR ISOLATION OF COAGULASE-POSITIVE STAPHYLOCOCCI

Carter, C. H. (1960) · Journal of Bacteriology · doi:10.1128/jb.79.5.753-754.1960 · Cited by 30 · see citing works

Simplified method for the isolation, identification, and characterization of Staphylococcus epidermidis in epidemiologic studies

Parisi, J. T., & Hamory, B. H. (1986) · Diagnostic Microbiology and Infectious Disease · doi:10.1016/0732-8893(86)90053-2 · Cited by 16 · see citing works

Rapid identification and specific quantification of Staphylococcus epidermidis by 5′ nuclease real-time polymerase chain reaction with a minor groove binder probe

Iwase, T., Hoshina, S., Seki, K., Shinji, H., Masuda, S., & Mizunoe, Y. (2007) · Diagnostic Microbiology and Infectious Disease · doi:10.1016/j.diagmicrobio.2007.08.009 · Cited by 14 · see citing works

Correction: Effects of the Staphylococcus aureus and Staphylococcus epidermidis Secretomes Isolated from the Skin Microbiota of Atopic Children on CD4+ T Cell Activation

Laborel-Préneron, E., Bianchi, P., Boralévi, F., Lehours, P., Fraysse, F., Morice‐Picard, F., Sugai, M., Sato’o, Y., Badiou, C., Lina, G., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0144323 · Cited by 9 · see citing works

Seven years of L-dopa therapy

Robertson, M. G. (1974) · Nature · doi:10.1038/250104a0 · Cited by 3 · see citing works

Interaction between microbiota and immunity in health and disease

Zheng, D., Liwinski, T., & Elinav, E. (2020) · Cell Research · doi:10.1038/s41422-020-0332-7 · Cited by 3,947 · see citing works

The human skin microbiome

Byrd, A. L., Belkaid, Y., & Segre, J. A. (2018) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2017.157 · Cited by 2,806 · see citing works

Antimicrobial host defence peptides: functions and clinical potential

Mookherjee, N., Anderson, M. A., Haagsman, H. P., & Davidson, D. J. (2020) · Nature Reviews Drug Discovery · doi:10.1038/s41573-019-0058-8 · Cited by 1,502 · see citing works

Does the epithelial barrier hypothesis explain the increase in allergy, autoimmunity and other chronic conditions?

Akdiş, C. A. (2021) · Nature reviews. Immunology · doi:10.1038/s41577-021-00538-7 · Cited by 1,016 · see citing works

The gut microbiome: Relationships with disease and opportunities for therapy

Durack, J., & Lynch, S. V. (2018) · The Journal of Experimental Medicine · doi:10.1084/jem.20180448 · Cited by 955 · see citing works

Skin microbiota–host interactions

Chen, Y. E., Fischbach, M. A., & Belkaid, Y. (2018) · Nature · doi:10.1038/nature25177 · Cited by 788 · see citing works

The Dynamics of the Skin’s Immune System

Nguyen, A. V., & Soulika, A. M. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20081811 · Cited by 719 · see citing works

Microbiota and maintenance of skin barrier function

Harris-Tryon, T. A., & Grice, E. A. (2022) · Science · doi:10.1126/science.abo0693 · Cited by 656 · see citing works

Shaping the Future of Probiotics and Prebiotics

Cunningham, M., Azcarate-Peril, M. A., Barnard, A., Benoit, V., Grimaldi, R., Guyonnet, D., Holscher, H. D., Hunter, K., Manurung, S., Obis, D., et al. (2021) · Trends in Microbiology · doi:10.1016/j.tim.2021.01.003 · Cited by 637 · see citing works

Pathophysiology of atopic dermatitis: Clinical implications

Kim, J., Kim, B. E., & Leung, D. Y. M. (2019) · Allergy and Asthma Proceedings · doi:10.2500/aap.2019.40.4202 · Cited by 652 · see citing works

Gut–Skin Axis: Current Knowledge of the Interrelationship between Microbial Dysbiosis and Skin Conditions

Pessemier, B. D., Grine, L., Debaere, M., Maes, A., Paetzold, B., & Callewaert, C. (2021) · Microorganisms · doi:10.3390/microorganisms9020353 · Cited by 661 · see citing works

Staphylococcus aureus and Staphylococcus epidermidis strain diversity underlying pediatric atopic dermatitis

Byrd, A. L., Deming, C., Cassidy, S. K. B., Harrison, O. J., Ng, W.-I., Conlan, S., Program, N. C. S., Belkaid, Y., Segre, J. A., & Kong, H. H. (2017) · Science Translational Medicine · doi:10.1126/scitranslmed.aal4651 · Cited by 596 · see citing works

New Insights into Human Nostril Microbiome from the Expanded Human Oral Microbiome Database (eHOMD): a Resource for the Microbiome of the Human Aerodigestive Tract

Escapa, I. F., Chen, T., Huang, Y., Gajare, P., Dewhirst, F. E., & Lemon, K. P. (2018) · mSystems · doi:10.1128/msystems.00187-18 · Cited by 593 · see citing works

The Evolution and Ecology of Bacterial Warfare

Granato, E. T., Meiller-Legrand, T. A., & Foster, K. R. (2019) · Current Biology · doi:10.1016/j.cub.2019.04.024 · Cited by 496 · see citing works

Mass spectrometry-based metabolomics in microbiome investigations

Bauermeister, A., Mannochio-Russo, H., Costa-Lotufo, L. V., Jarmusch, A. K., & Dorrestein, P. C. (2021) · Nature Reviews Microbiology · doi:10.1038/s41579-021-00621-9 · Cited by 538 · see citing works

The microbiome in patients with atopic dermatitis

Paller, A. S., Kong, H. H., Seed, P., Naik, S., Scharschmidt, T. C., Gallo, R. L., Luger, T., & Irvine, A. D. (2019) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2018.11.015 · Cited by 525 · see citing works

Staphylococcus aureus and Atopic Dermatitis: A Complex and Evolving Relationship

Geoghegan, J. A., Irvine, A. D., & Foster, T. J. (2017) · Trends in Microbiology · doi:10.1016/j.tim.2017.11.008 · Cited by 517 · see citing works

The Immune Functions of Keratinocytes in Skin Wound Healing

Piipponen, M., Li, D., & Xu, N. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21228790 · Cited by 521 · see citing works

Skin barrier immunity and ageing

Chambers, E. S., & Vukmanovic‐Stejic, M. (2019) · Immunology · doi:10.1111/imm.13152 · Cited by 505 · see citing works

Host–microbiota interactions in immune-mediated diseases

Ruff, W. E., Greiling, T. M., & Kriegel, M. A. (2020) · Nature Reviews Microbiology · doi:10.1038/s41579-020-0367-2 · Cited by 489 · see citing works

γδ T cells in homeostasis and host defence of epithelial barrier tissues

Nielsen, M. M., Witherden, D. A., & Havran, W. L. (2017) · Nature Reviews Immunology · doi:10.1038/nri.2017.101 · Cited by 479 · see citing works

Dupilumab with concomitant topical corticosteroid treatment in adults with atopic dermatitis with an inadequate response or intolerance to ciclosporin A or when this treatment is medically inadvisable: a placebo-controlled, randomized phase III clinical t

de Bruin-Weller, M. S., Thaçi, D., Smith, C. H., Reich, K., Cork, M. J., Radin, A. R., Zhang, Q., Akinlade, B. K., Gadkari, A., Eckert, L., et al. (2017) · British Journal of Dermatology · doi:10.1111/bjd.16156 · Cited by 479 · see citing works

Microbiota-mediated colonization resistance: mechanisms and regulation

Caballero-Flores, G., Pickard, J. M., & Núñez, G. (2023) · Nature Reviews Microbiology · doi:10.1038/s41579-022-00833-7 · Cited by 474 · see citing works

Towards Optimal pH of the Skin and Topical Formulations: From the Current State of the Art to Tailored Products

Lukić, M. Ž., Pantelić, I., & Savic, S. D. (2021) · Cosmetics · doi:10.3390/cosmetics8030069 · Cited by 474 · see citing works

The atopic march and atopic multimorbidity: many trajectories, many pathways

Paller, A. S., Spergel, J. M., Mina-Osorio, P., & Irvine, A. D. (2019) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2018.11.006 · Cited by 464 · see citing works

The social network of microorganisms — how auxotrophies shape complex communities

Zengler, K., & Zaramela, L. S. (2018) · Nature Reviews Microbiology · doi:10.1038/s41579-018-0004-5 · Cited by 448 · see citing works

Microbe-host interplay in atopic dermatitis and psoriasis

Fyhrquist, N., Muirhead, G., Prast‐Nielsen, S., Jeanmougin, M., Oláh, P., Skoog, T., Jules-Clément, G., Feld, M., Barrientos‐Somarribas, M., Sinkko, H., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-12253-y · Cited by 416 · see citing works

Challenges, Progress, and Prospects of Developing Therapies to Treat Autoimmune Diseases

Fugger, L. H., Jensen, L. T., & Rossjohn, J. (2020) · Cell · doi:10.1016/j.cell.2020.03.007 · Cited by 403 · see citing works

The microbiome-shaping roles of bacteriocins

Heilbronner, S., Krismer, B., Brötz‐Oesterhelt, H., & Peschel, A. (2021) · Nature Reviews Microbiology · doi:10.1038/s41579-021-00569-w · Cited by 398 · see citing works

Significance of Skin Barrier Dysfunction in Atopic Dermatitis

Kim, B. E., & Leung, D. Y. M. (2018) · Allergy, Asthma &amp; Immunology Research · doi:10.4168/aair.2018.10.3.207 · Cited by 393 · see citing works

Type 2 immunity in allergic diseases

Öğülür, İ., Mitamura, Y., Yazıcı, D., Pat, Y., Ardıçlı, S., Li, M., D’Avino, P., Beha, C., Babayev, H., Zhao, B., et al. (2025) · Cellular and Molecular Immunology · doi:10.1038/s41423-025-01261-2 · Cited by 413 · see citing works

Interleukin‐13: Targeting an underestimated cytokine in atopic dermatitis

Bieber, T. (2020) · Allergy · doi:10.1111/all.13954 · Cited by 382 · see citing works

The commensal lifestyle of Staphylococcus aureus and its interactions with the nasal microbiota

Krismer, B., Weidenmaier, C., Zipperer, A., & Peschel, A. (2017) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2017.104 · Cited by 376 · see citing works

Staphylococcus epidermidis and its dual lifestyle in skin health and infection

Severn, M. M., & Horswill, A. R. (2022) · Nature Reviews Microbiology · doi:10.1038/s41579-022-00780-3 · Cited by 386 · see citing works

Human Skin Microbiome: Impact of Intrinsic and Extrinsic Factors on Skin Microbiota

Skowron, K., Bauza-Kaszewska, J., Kraszewska, Z., Wiktorczyk-Kapischke, N., Grudlewska‐Buda, K., Kwiecińska-Piróg, J., Wałecka-Zacharska, E., Radtke, L., & Gospodarek-Komkowska, E. (2021) · Microorganisms · doi:10.3390/microorganisms9030543 · Cited by 360 · see citing works

Host-microbiome interactions and recent progress into understanding the biology of acne vulgaris

O’Neill, A. M., & Gallo, R. L. (2018) · Microbiome · doi:10.1186/s40168-018-0558-5 · Cited by 334 · see citing works

Development of a human skin commensal microbe for bacteriotherapy of atopic dermatitis and use in a phase 1 randomized clinical trial

Nakatsuji, T., Hata, T. R., Tong, Y., Cheng, J. Y., Shafiq, F., Butcher, A. M., Salem, S. S., Brinton, S. L., Rudman Spergel, A. K., Johnson, K., et al. (2021) · Nature Medicine · doi:10.1038/s41591-021-01256-2 · Cited by 333 · see citing works

The microbiome in allergic disease: Current understanding and future opportunities—2017 PRACTALL document of the American Academy of Allergy, Asthma &amp; Immunology and the European Academy of Allergy and Clinical Immunology

Huang, Y. J., Marsland, B. J., Bunyavanich, S., O'Mahony, L., Leung, D. Y. M., Muraro, A., & Fleisher, T. A. (2017) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2017.02.007 · Cited by 330 · see citing works

First-in-human topical microbiome transplantation with Roseomonas mucosa for atopic dermatitis

Myles, I. A., Earland, N. J., Anderson, E. D., Moore, I. N., Kieh, M. D., Williams, K. W., Saleem, A., Fontecilla, N. M., Welch, P. A., Darnell, D. A., et al. (2018) · JCI Insight · doi:10.1172/jci.insight.120608 · Cited by 332 · see citing works

Microbiome in the gut-skin axis in atopic dermatitis

Lee, S.-Y., Lee, E., Park, Y. M., & Hong, S.-J. (2018) · Allergy, Asthma &amp; Immunology Research · doi:10.4168/aair.2018.10.4.354 · Cited by 326 · see citing works

A commensal strain of Staphylococcus epidermidis protects against skin neoplasia

Nakatsuji, T., Chen, T. H., Butcher, A. M., Trzoss, L., Nam, S., Shirakawa, K. T., Zhou, W. L., Oh, J., Otto, M. J., Fenical, W., et al. (2018) · Science Advances · doi:10.1126/sciadv.aao4502 · Cited by 327 · see citing works

Skin Barrier Function and the Microbiome

Lee, H.-J., & Kim, M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113071 · Cited by 317 · see citing works

Cutaneous Barriers and Skin Immunity: Differentiating A Connected Network

Eyerich, S., Eyerich, K., Traidl‐Hoffmann, C., & Biedermann, T. (2018) · Trends in Immunology · doi:10.1016/j.it.2018.02.004 · Cited by 306 · see citing works

Gut microbiota as a source of novel antimicrobials

García-Gutiérrez, E., Mayer, M. J., Cotter, P. D., & Narbad, A. (2018) · Gut Microbes · doi:10.1080/19490976.2018.1455790 · Cited by 295 · see citing works

Acne, the Skin Microbiome, and Antibiotic Treatment

Xu, H., & Li, H. (2019) · American Journal of Clinical Dermatology · doi:10.1007/s40257-018-00417-3 · Cited by 294 · see citing works

Quorum sensing between bacterial species on the skin protects against epidermal injury in atopic dermatitis

Williams, M. R., Costa, S. K., Zaramela, L. S., Khalil, S., Todd, D. A., Winter, H. L., Sanford, J. A., O’Neill, A. M., Liggins, M. C., Nakatsuji, T., et al. (2019) · Science Translational Medicine · doi:10.1126/scitranslmed.aat8329 · Cited by 292 · see citing works

Atopic dermatitis: the skin barrier and beyond

Tsakok, T., Woolf, R., Smith, C. H., Weidinger, S., & Flohr, C. (2018) · British Journal of Dermatology · doi:10.1111/bjd.16934 · Cited by 298 · see citing works

Commensal Staphylococcus epidermidis contributes to skin barrier homeostasis by generating protective ceramides

Zheng, Y., Hunt, R. L., Villaruz, A. E., Fisher, E. L., Liu, R., Liu, Q., Cheung, G. Y. C., Li, M., & Otto, M. J. (2022) · Cell Host & Microbe · doi:10.1016/j.chom.2022.01.004 · Cited by 291 · see citing works

Microbiota-derived lantibiotic restores resistance against vancomycin-resistant Enterococcus

Kim, S. G., Becattini, S., Moody, T. U., Shliaha, P. V., Littmann, E. R., Seok, R., Gjonbalaj, M., Eaton, V. P., Fontana, E., Amoretti, L. A., et al. (2019) · Nature · doi:10.1038/s41586-019-1501-z · Cited by 280 · see citing works

The Skin Microbiota: Balancing Risk and Reward

Flowers, L. J., & Grice, E. A. (2020) · Cell Host & Microbe · doi:10.1016/j.chom.2020.06.017 · Cited by 284 · see citing works

Commensal Staphylococci Influence Staphylococcus aureus Skin Colonization and Disease

Parlet, C. P., Severn, M. M., & Horswill, A. R. (2019) · Trends in Microbiology · doi:10.1016/j.tim.2019.01.008 · Cited by 275 · see citing works

Major Comorbidities of Atopic Dermatitis: Beyond Allergic Disorders

Paller, A. S., Jaworski, J. C., Simpson, E. L., Boguniewicz, M., Russell, J. J., Block, J. K., Tofte, S. J., Dunn, J. D., Feldman, S. R., Clark, A. R., et al. (2018) · American Journal of Clinical Dermatology · doi:10.1007/s40257-018-0383-4 · Cited by 281 · see citing works

The Potential of Human Peptide LL-37 as an Antimicrobial and Anti-Biofilm Agent

Ridyard, K. E., & Overhage, J. (2021) · Antibiotics · doi:10.3390/antibiotics10060650 · Cited by 273 · see citing works

A systematic framework for understanding the microbiome in human health and disease: from basic principles to clinical translation

Ma, Z., Zuo, T., Frey, N., & Rangrez, A. Y. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01946-6 · Cited by 297 · see citing works

Epithelial barrier repair and prevention of allergy

Goleva, E., Berdyshev, E., & Leung, D. Y. M. (2019) · Journal of Clinical Investigation · doi:10.1172/jci124608 · Cited by 251 · see citing works

Type 2 Inflammation Contributes to Skin Barrier Dysfunction in Atopic Dermatitis

Beck, L. A., Cork, M. J., Amagai, M., Benedetto, A. D., Kabashima, K., Hamilton, J. D., & Rossi, A. B. (2022) · JID Innovations · doi:10.1016/j.xjidi.2022.100131 · Cited by 258 · see citing works

Challenges in exploring and manipulating the human skin microbiome

Boxberger, M., Cenizo, V., Cassir, N., & La Scola, B. (2021) · Microbiome · doi:10.1186/s40168-021-01062-5 · Cited by 247 · see citing works

Coagulase-Negative Staphylococcal Strain Prevents Staphylococcus aureus Colonization and Skin Infection by Blocking Quorum Sensing

Paharik, A. E., Parlet, C. P., Chung, N., Todd, D. A., Rodriguez, E. I., Dyke, M. J. V., Cech, N. B., & Horswill, A. R. (2017) · Cell Host & Microbe · doi:10.1016/j.chom.2017.11.001 · Cited by 240 · see citing works

Microbiome of the Skin and Gut in Atopic Dermatitis (AD): Understanding the Pathophysiology and Finding Novel Management Strategies

Kim, J. E., & Kim, H. S. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8040444 · Cited by 244 · see citing works

The translational revolution in atopic dermatitis: the paradigm shift from pathogenesis to treatment

Facheris, P., Jeffery, J., DUCA, E. D., & Guttman‐Yassky, E. (2023) · Cellular and Molecular Immunology · doi:10.1038/s41423-023-00992-4 · Cited by 247 · see citing works

The impact of skin care products on skin chemistry and microbiome dynamics

Bouslimani, A., da Silva, R., Kosciolek, T., Janssen, S., Callewaert, C., Amir, A., Dorrestein, K., Melnik, A. V., Zaramela, L. S., Kim, J.-N., et al. (2019) · BMC Biology · doi:10.1186/s12915-019-0660-6 · Cited by 234 · see citing works

The Skin and Gut Microbiome and Its Role in Common Dermatologic Conditions

Ellis, S. R., Nguyen, M., Vaughn, A. R., Notay, M., Burney, W. A., Sandhu, S., & Sivamani, R. K. (2019) · Microorganisms · doi:10.3390/microorganisms7110550 · Cited by 236 · see citing works

Staphylococcus epidermidis and Cutibacterium acnes: Two Major Sentinels of Skin Microbiota and the Influence of Cosmetics

Fournière, M., Latire, T., Souak, D., Feuilloley, M. G. J., & Bedoux, G. (2020) · Microorganisms · doi:10.3390/microorganisms8111752 · Cited by 227 · see citing works

Propionibacterium acnes and Acne Vulgaris: New Insights from the Integration of Population Genetic, Multi-Omic, Biochemical and Host-Microbe Studies

McLaughlin, J. B., Watterson, S., Layton, A., Bjourson, A. J., Barnard, E., & McDowell, A. (2019) · Microorganisms · doi:10.3390/microorganisms7050128 · Cited by 233 · see citing works

IL-4Rα Blockade by Dupilumab Decreases Staphylococcus aureus Colonization and Increases Microbial Diversity in Atopic Dermatitis

Callewaert, C., Nakatsuji, T., Knight, R. D., Kościółek, T., Vrbanac, A. F., Kotol, P. F., Ardeleanu, M., Hultsch, T., Guttman‐Yassky, E., Bissonnette, R., et al. (2019) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2019.05.024 · Cited by 226 · see citing works

The nonlesional skin surface distinguishes atopic dermatitis with food allergy as a unique endotype

Leung, D. Y. M., Calatroni, A., Zaramela, L. S., LeBeau, P. K., Dyjack, N., Brar, K., David, G., Johnson, K., Leung, S., Ramirez-Gama, M., et al. (2019) · Science Translational Medicine · doi:10.1126/scitranslmed.aav2685 · Cited by 214 · see citing works

Bacterial Biofilm in Chronic Wounds and Possible Therapeutic Approaches

Cavallo, I., Sivori, F., Mastrofrancesco, A., Abril, E., Pontone, M., Domenico, E. G. D., & Pimpinelli, F. (2024) · Biology · doi:10.3390/biology13020109 · Cited by 227 · see citing works

Atopic dermatitis: Role of the skin barrier, environment, microbiome, and therapeutic agents

Luger, T. A., Amagai, M., Dréno, B., Dagnelie, M., Liao, W. J., Kabashima, K., Schikowski, T., Proksch, E., Elias, P. M., Simon, M., et al. (2021) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2021.04.007 · Cited by 217 · see citing works

Interactions Between Atopic Dermatitis and Staphylococcus aureus Infection: Clinical Implications

Kim, J., Kim, B. E., Ahn, K., & Leung, D. Y. M. (2019) · Allergy Asthma and Immunology Research · doi:10.4168/aair.2019.11.5.593 · Cited by 212 · see citing works

The role of bacterial skin infections in atopic dermatitis: expert statement and review from the International Eczema Council Skin Infection Group

Alexander, H., Paller, A. S., Traidl‐Hoffmann, C., Beck, L. A., Benedetto, A. D., Dhar, S., Girolomoni, G., Irvine, A. D., Spuls, P. I., Su, J. C., et al. (2019) · British Journal of Dermatology · doi:10.1111/bjd.18643 · Cited by 209 · see citing works

New treatments in atopic dermatitis

Puar, N. K., Chovatiya, R., & Paller, A. S. (2020) · Annals of Allergy Asthma & Immunology · doi:10.1016/j.anai.2020.08.016 · Cited by 205 · see citing works

Commensal microbiota modulate gene expression in the skin

Meisel, J. S., Sfyroera, G., Bartow-McKenney, C., Gimblet, C., Bugayev, J., Horwinski, J., Kim, B., Brestoff, J. R., Tyldsley, A. S., Zheng, Q., et al. (2018) · Microbiome · doi:10.1186/s40168-018-0404-9 · Cited by 201 · see citing works

Report from the National Institute of Allergy and Infectious Diseases workshop on “Atopic dermatitis and the atopic march: Mechanisms and interventions”

Davidson, W. F., Leung, D. Y. M., Beck, L. A., Berin, M. C., Boguniewicz, M., Busse, W. W., Chatila, T. A., Geha, R. S., Gern, J. E., Guttman‐Yassky, E., et al. (2019) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2019.01.003 · Cited by 201 · see citing works

Therapeutic pipeline for atopic dermatitis: End of the drought?

Paller, A. S., Kabashima, K., & Bieber, T. (2017) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2017.07.006 · Cited by 192 · see citing works

Epidermal lipid composition, barrier integrity, and eczematous inflammation are associated with skin microbiome configuration

Baurecht, H., Rühlemann, M. C., Rodríguez, E., Thielking, F., Harder, I., Erkens, A., Stölzl, D., Ellinghaus, E., Hotze, M., Lieb, W., et al. (2018) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2018.01.019 · Cited by 193 · see citing works

Staphylococcus epidermidis—Skin friend or foe?

Severn, M. M., & Horswill, A. R. (2020) · PLoS Pathogens · doi:10.1371/journal.ppat.1009026 · Cited by 194 · see citing works

The Skin Microbiome: Current Landscape and Future Opportunities

Smythe, P., & Wilkinson, H. N. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24043950 · Cited by 207 · see citing works

Cutaneous barrier dysfunction in allergic diseases

Leung, D. Y. M., Berdyshev, E., & Goleva, E. (2020) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2020.02.021 · Cited by 190 · see citing works

Patients with Atopic Dermatitis Colonized with Staphylococcus aureus Have a Distinct Phenotype and Endotype

Simpson, E. L., Villarreal, M., Jepson, B. M., Rafaels, N., David, G. L., Hanifin, J. M., Taylor, P. A., Boguniewicz, M., Yoshida, T., Benedetto, A. D., et al. (2018) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2018.03.1517 · Cited by 193 · see citing works

Staphylococcus epidermidis protease EcpA can be a deleterious component of the skin microbiome in atopic dermatitis

Cau, L., Williams, M. R., Butcher, A. M., Nakatsuji, T., Kavanaugh, J. S., Cheng, J. Y., Shafiq, F., Higbee, K., Hata, T. R., Horswill, A. R., et al. (2020) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2020.06.024 · Cited by 187 · see citing works

A Vehicle‐Free Antimicrobial Polymer Hybrid Gold Nanoparticle as Synergistically Therapeutic Platforms for Staphylococcus aureus Infected Wound Healing

He, X., Dai, L., Ye, L., Sun, X., Obeng, E., Hu, R., Zan, X., Lin, F., & Shen, J. (2022) · Advanced Science · doi:10.1002/advs.202105223 · Cited by 186 · see citing works

Staphylococcus aureus colonisation and strategies for decolonisation

Piewngam, P., & Otto, M. J. (2024) · The Lancet Microbe · doi:10.1016/s2666-5247(24)00040-5 · Cited by 189 · see citing works

From Dysbiosis to Healthy Skin: Major Contributions of Cutibacterium acnes to Skin Homeostasis

Rozas, M., de Ruijter, A. B. P. H., Fábrega, M.-J., Zorgani, A., Güell, M., Paetzold, B., & Brillet, F. (2021) · Microorganisms · doi:10.3390/microorganisms9030628 · Cited by 182 · see citing works

Living in Your Skin: Microbes, Molecules, and Mechanisms

Swaney, M. H., & Kalan, L. (2021) · Infection and Immunity · doi:10.1128/iai.00695-20 · Cited by 187 · see citing works

Skin microbiome of atopic dermatitis

Koh, L. F., Ong, R. Y., & Common, J. (2021) · Allergology International · doi:10.1016/j.alit.2021.11.001 · Cited by 182 · see citing works

Interplay between gut microbiota and antimicrobial peptides

Zong, X., Fu, J., Xu, B., Wang, Y., & Jin, M. (2020) · Animal nutrition · doi:10.1016/j.aninu.2020.09.002 · Cited by 179 · see citing works

Probiotics or pro‐healers: the role of beneficial bacteria in tissue repair

Lukić, J., Chen, V., Strahinić, I., Begović, J., Lev‐Tov, H. A., Davis, S. C., Tomic‐Canic, M., & Pastar, I. (2017) · Wound Repair and Regeneration · doi:10.1111/wrr.12607 · Cited by 175 · see citing works

Skin Microbiome in Atopic Dermatitis

Edslev, S. M., Agner, T., & Andersen, P. S. (2020) · Acta Dermato Venereologica · doi:10.2340/00015555-3514 · Cited by 182 · see citing works

Skin and Gut Microbiome in Psoriasis: Gaining Insight Into the Pathophysiology of It and Finding Novel Therapeutic Strategies

Chen, L., Li, J., Zhu, W., Kuang, Y., Liu, T., Zhang, W., Chen, X., & Peng, C. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.589726 · Cited by 175 · see citing works

A Cutibacterium acnes antibiotic modulates human skin microbiota composition in hair follicles

Claesen, J., Spagnolo, J., Ramos, S. F., Kurita, K. L., Byrd, A. L., Aksenov, A. A., Melnik, A. V., Wong, W. R., Wang, S., Hernandez, R. D., et al. (2020) · Science Translational Medicine · doi:10.1126/scitranslmed.aay5445 · Cited by 166 · see citing works

The skin microbiome and the gut-skin axis

Sinha, S., Lin, G. H. Y., & Ferenczi, K. (2021) · Clinics in Dermatology · doi:10.1016/j.clindermatol.2021.08.021 · Cited by 189 · see citing works

The Human Skin Microbiome in Selected Cutaneous Diseases

Carmona-Cruz, S., Orozco-Covarrubias, L., & Sáez-de-Ocariz, M. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.834135 · Cited by 170 · see citing works

Association of Disease Severity With Skin Microbiome and Filaggrin Gene Mutations in Adult Atopic Dermatitis

Clausen, M., Agner, T., Lilje, B., Edslev, S. M., Johannesen, T. B., & Andersen, P. S. (2018) · JAMA Dermatology · doi:10.1001/jamadermatol.2017.5440 · Cited by 168 · see citing works

Immunologic, microbial, and epithelial interactions in atopic dermatitis

Brunner, P. M., Leung, D. Y. M., & Guttman‐Yassky, E. (2017) · Annals of Allergy Asthma & Immunology · doi:10.1016/j.anai.2017.09.055 · Cited by 164 · see citing works

The role of the skin microbiome in atopic dermatitis

Nakatsuji, T., & Gallo, R. L. (2018) · Annals of Allergy Asthma & Immunology · doi:10.1016/j.anai.2018.12.003 · Cited by 165 · see citing works

Human skin microbiota is a rich source of bacteriocin-producing staphylococci that kill human pathogens

O'Sullivan, J. N., Rea, M. C., O’Connor, P. M., Hill, C., & Ross, R. P. (2018) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiy241 · Cited by 164 · see citing works

Unmet medical needs in chronic, non-communicable inflammatory skin diseases

Ujiie, H., Rosmarin, D., Schön, M. P., Ständer, S., Boch, K., Metz, M., Maurer, M., Thaci, D., Schmidt, E., Cole, C., et al. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2022.875492 · Cited by 158 · see citing works

Cutaneous Malassezia: Commensal, Pathogen, or Protector?

Chandra, S. H. V., Srinivas, R., Dawson, T. L., & Common, J. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.614446 · Cited by 161 · see citing works

Elucidation of complexity and prediction of interactions in microbial communities

Zúñiga, C., Zaramela, L. S., & Zengler, K. (2017) · Microbial Biotechnology · doi:10.1111/1751-7915.12855 · Cited by 152 · see citing works

Fecal Microbiota Transplantation as New Therapeutic Avenue for Human Diseases

Biazzo, M., & Deidda, G. (2022) · Journal of Clinical Medicine · doi:10.3390/jcm11144119 · Cited by 166 · see citing works

Skin’s Natural Bacteria May Protect Against Pathogens

Hampton, T. (2017) · JAMA · doi:10.1001/jama.2017.3111

Le microbiote cutané: le poids lourd sort de l'ombre [The skin microbiota: a colossus steps into the spotlight]

Di Domizio, J., Pagnoni, A., Huber, M., Hohl, D., & Gilliet, M. (2016) · SERVAL (Université de Lausanne)

Bacterial battles on your skin

Pujanandez, L. (2017) · Science · doi:10.1126/science.355.6327.808-b

Skin cream kills pathogen

(2017) · Nature · doi:10.1038/543008d

The role of skin dysbiosis in atopic dermatitis

Braun, C., Patra, V., Lina, G., Nicolas, J., Vocanson, M., & Nosbaum, A. (2022) · European Journal of Dermatology · doi:10.1684/ejd.2022.4289 · Cited by 12 · see citing works