Annals of Allergy Asthma & Immunology, Journal Year: 2018, Volume and Issue: 122(3), P. 263 - 269
Published: Dec. 11, 2018
Language: Английский
Annals of Allergy Asthma & Immunology, Journal Year: 2018, Volume and Issue: 122(3), P. 263 - 269
Published: Dec. 11, 2018
Language: Английский
International Journal of Molecular Sciences, Journal Year: 2019, Volume and Issue: 20(8), P. 1811 - 1811
Published: April 12, 2019
The skin is a complex organ that has devised numerous strategies, such as physical, chemical, and microbiological barriers, to protect the host from external insults. In addition, contains an intricate network of immune cells resident tissue, crucial for defense well tissue homeostasis. event insult, skin-resident are not only prevention infection but also reconstruction. Deregulation responses often leads impaired healing poor restoration function. this review, we will discuss defensive components focus on function in homeostasis their role wound healing.
Language: Английский
Citations
519Journal of Allergy and Clinical Immunology, Journal Year: 2018, Volume and Issue: 143(1), P. 26 - 35
Published: Nov. 23, 2018
As an interface with the environment, skin is a complex ecosystem colonized by many microorganisms that coexist in established balance. The cutaneous microbiome inhibits colonization pathogens, such as Staphylococcus aureus, and crucial component for function of epidermal barrier. Moreover, crosstalk between commensals immune system now recognized because can modulate both innate adaptive responses. Host-commensal interactions also have effect on developing infants and, subsequently, occurrence diseases, asthma atopic dermatitis (AD). Later life, contributes to development course disease. Accordingly, patients AD, decrease diversity correlates disease severity increased pathogenic bacteria, S aureus. Early clinical studies suggest topical application commensal organisms (eg, hominis or Roseomonas mucosa) reduces AD severity, which supports important role decreasing aureus AD. Advancing knowledge its modulating disorders, might result novel therapeutic strategies. A multitude microbiota inhabit our human epithelial surfaces. Although there increasing evidence these microbiota, live bodies, are health disease, functions consequences resident remain poorly understood. Given challenges being able adequately culture all microbes present given sample, technological advances genome sequencing ability interrogate microbiomes (the full collection microbiota). Several technical study composition collectively enlightened understanding pathogenesis (AD) modification (Fig 1).1Byrd A.L. Belkaid Y. Segre J.A. microbiome.Nat Rev Microbiol. 2018; 16: 143-155Crossref PubMed Scopus (917) Google Scholar animal models cannot fully recapitulate states, use model deeply investigate host-microbial relationships has elucidated intriguing biological mechanisms. continued integration gleaned from patient-derived models, will be critical approaches. Prior publications extensively reviewed differences based various factors, including anatomic sites, sexual maturity, physiology; this review provides broad overview different aspects microbiome, immunology, microbiology, barrier research related particular early host-microbiome events Here we healthy skin. complexities microbial communities reflected distinct observed skin, gut, respiratory tract, among other body sites. Furthermore, niches undergo changes over lifespan. continual potential roles subsequently lead preventative and/or Skin highlighted site specificity subjects, regional surfaces compositions communities.2Findley K. Oh J. Yang Conlan S. Deming C. Meyer et al.Topographic fungal bacterial skin.Nature. 2013; 498: 367-370Crossref (731) Scholar, 3Grice E.A. Kong H.H. C.B. Davis Young A.C. al.Topographical temporal microbiome.Science. 2009; 324: 1190-1192Crossref (1840) 4Oh Byrd NISC program al.Biogeography individuality shape metagenome.Nature. 2014; 514: 59-64Crossref (624) 5Costello E.K. Lauber C.L. Hamady M. Fierer N. Gordon J.I. Knight R. Bacterial community variation habitats across space time.Science. 326: 1694-1697Crossref (2181) hosts most diverse body, more than 1000 species 19 phyla.3Grice 6Kong molecular revolution biology: investigating microbiome.J Invest Dermatol. 2017; 137: e119-e122Abstract Full Text PDF (31) unique features specific some shared reflect physiology: sebaceous sites often Cutibacterium acnes (formerly known Propionibacterium acnes). Small adult volunteers shown relatively stable months years each person possess personalized microbiome.7Oh Park Comparative Sequencing Program Temporal stability microbiome.Cell. 2016; 165: 854-866Abstract (495) Studies demonstrated subjects at life stages. For example, children who less sexually mature lower relative abundances Corynebacterium species8Oh Polley E.C. Shifts nares adults.Genome Med. 2012; 4: 77Crossref (224) greater fungi9Jo J.H. Kennedy Ng W.L. al.Diverse converge adulthood.J 136: 2356-2363Abstract (86) compared subjects. infant particularly active area investigation it provide insights into early-life exposures.10Capone K.A. Dowd S.E. Stamatas G.N. Nikolovski Diversity life.J 2011; 131: 2026-2032Abstract (302) 11Costello Carlisle E.M. Bik Morowitz M.J. Relman D.A. Microbiome assembly multiple low-birthweight infants.MBio. 4 (e00782-13)Crossref (106) 12Dominguez-Bello M.G. Costello Contreras Magris Hidalgo G. al.Delivery mode shapes acquisition structure initial newborns.Proc Natl Acad Sci U A. 2010; 107: 11971-11975Crossref (2958) 13Kennedy Connolly Hourihane J.O. Fallon P.G. McLean W.H. Murray D. al.Skin before dermatitis: staphylococci 2 associated risk 1 year.J Allergy Clin Immunol. 139: 166-172Abstract (206) Children young days old site-specific their microbiomes13Kennedy influence future disease.14Shi B. Bangayan N.J. Curd E. Taylor P.A. Gallo R.L. Leung D.Y.M. al.The pediatric versus dermatitis.J 138: 1233-1236Abstract (92) 15Chu D.M. Ma Prince Antony K.M. Seferovic M.D. Aagaard Maturation relation delivery.Nat 23: 314-326Crossref (556) characterized rapid immunologic maturation. such, represents period during host-commensal formatively affect how responds brethren.16Kollmann T.R. Levy O. Montgomery R.R. Goriely Innate Toll-like receptors: responses newborns elderly.Immunity. 37: 771-783Abstract (378) 17McGovern Shin Low Duan Yao L.J. al.Human fetal dendritic cells promote prenatal T-cell suppression through arginase-2.Nature. 546: 662-666Crossref (157) Future success microbially directed interventions prevent treat inflammatory require deeper mechanisms responsible symbiosis window. Neonatal demonstrate reduced propensity activation inflammation those adults. We appreciate not only due immaturity but existence regulatory In infants, older adults, receptors (TLRs), key sensors system, results production IL-6 IL-23 TNF-α IL-1.16Kollmann Composition evolves parallel, T (Treg) found abundance infancy.17McGovern 18Yang Fujikado Kolodin Benoist Mathis Immune tolerance. Regulatory generated play maintaining self-tolerance.Science. 2015; 348: 589-594Crossref (283) 19Thome J.J.C. Bickham K.L. Ohmura Kubota Matsuoka al.Early-life compartmentalization cell differentiation mucosal lymphoid tissues.Nat 22: 72-77Crossref (201) place neonates disseminated infection, they tolerance self-antigens foreign antigens, thereby preventing disadvantageous tissue development. Birth marks abrupt transition, exposure products antigens. seen later influenced, least initially, exogenous birth delivery maternal commensals.10Capone Notably, identity host trajectory. gut- lung-resident been susceptibility colitis, asthma, anaphylaxis.20Gensollen T. Iyer S.S. Kasper D.L. Blumberg R.S. How system.Science. 352: 539-544Crossref (956) presence absence certain gut bacteria proinflammatory metabolites heightened asthma.21Fujimura K.E. Sitarik A.R. Havstad Lin Levan Fadrosh al.Neonatal associates childhood multisensitized atopy differentiation.Nat 1187-1191Crossref (586) Whether disruption directly affects remains open question. However, notable recent longitudinal examining alterations flora predate onset.13Kennedy 22Meylan P. Lang Mermoud Johannsen Norrenberg Hohl precedes diagnosis infancy.J 2497-2504Abstract (143) Until recently, little was about exposures function. Modeling relationship mice taught us likely equal significance tissues. When neonatal bacterium (coagulase-negative [CoNS]) epidermidis, develop large percentage Treg epidermidis mount microbe rechallenge life. contrast, delaying until adulthood prevents protective promotes otherwise "healthy" 2).22Meylan At factor accounting age-dependent difference density skin.23Scharschmidt T.C. Vasquez K.S. Truong H.-A. Gearty S.V. Pauli M.L. Nosbaum al.A wave t mediates microbes.Immunity. 43: 1011-1021Abstract (328) Intriguingly, markedly decreased raised under gnotobiotic ("germ-free") conditions lacking hair follicles, major niche CoNS species. Indeed, follicles appears stimulate isthmus keratinocytes chemokine, CCL20, then helps recruit 2, left panel).24Scharschmidt Leitner E.G. Chu al.Commensal follicle morphogenesis coordinately drive migration skin.Cell Host Microbe. 21: 467-477Abstract (145) Thus promoting establishment preferentially facilitated themselves. Of course, regard timing development, communities, structure. findings translate biology implications disrupting fruitful investigation. detailed phenotyping yet undertaken, enriched skin.25Cordoro Hitraya-Low Taravati Sandoval P.M. Kim Sugarman al.Skin-infiltrating, interleukin-22-producing differentiate psoriasis psoriasis.J Am 77: 417-424Abstract (33) considering translational applications research, one envision corrective measures reduce onset mitigate severity. latter especially relevant variable penetrance genetic age defining features.26Weidinger Beck L.A. Bieber Kabashima Irvine A.D. Atopic dermatitis.Nat Dis Primers. 1Crossref (273) Continued work define function, context barrier-disrupted inform prevention-oriented recommendations microbe-based interventions. presents physical harmful agents while establishing regulate communities. contrast surfaces, maintain separation mucous layer, dense distribution appendages creates surface close communication microbes.27Gallo Human largest interaction microbes.J 1213-1214Abstract (124) strictly regulates sophisticated set antimicrobial gene include peptides proteins, lipids, pH barrier, free radical control community.28Zhang Antimicrobial peptides.Curr Biol. 26: R14-R19Abstract (518) network patrol reinforce pathogens penetrate epidermis after even minor breach.29Nakatsuji Chiang H.I. Jiang S.B. Nagarajan H. Zengler extends subepidermal compartments normal skin.Nat Commun. 1431Crossref (303) interplay defense, emerged balance disease.30Williams M.R. Nakatsuji aureus: master manipulator 579-581Abstract (41) 31Belkaid Dialogue immunity.Science. 346: 954-959Crossref (371) Mounting experimental suggests efficacious treatment conditions.32Grice microbiome: diagnostic approaches disease.Semin Cutan Med Surg. 33: 98-103Crossref (135) fundamental underlying immune-commensal beginning unfold. nuanced factors immunity offers opportunity harness power benefit. germ-free revealed optimal requires cues indigenous 2).33Naik Bouladoux Wilhelm Molloy Salcedo Kastenmuller W. al.Compartmentalized commensals.Science. 337: 1115-1119Crossref instance, effector make cytokines, IL-17A IFN-γ, dramatically abrogated commensals. This defect restored association commensal, residing intestine, highlighting nonredundant skin-resident modulation.33Naik 34Belkaid Naik Compartmentalized systemic commensals.Nat 14: 646-653Crossref (243) controls co-opting existing pathways, case IL-1α cells. skin-derived signals dispensable specification lymph node, commensally induced molecules entry sustain functions. Importantly, homeostatic tuning occurs overt intact barrier.35Naik Linehan J.L.1 Han S.J. Harrison O.J. Commensal-dendritic-cell specifies signature.Nature. 520: 104-108Crossref (470) lines advantageous support rich milieu elicit types Defined strains induce IL-17A, producing CD8 (TC17) reside epidermis.35Naik population actively cell–dependent antigen presentation N-formyl methionine peptides.36Linehan J.L. Vujkovic-Cvijin I. Villarino A.V. al.Non-classical impact repair.Cell. 172: 784-796Abstract (225) line findings, tropic produce IFN-γ response stimulation antigen.37Schlapbach Gehad Watanabe Guenova Teague J.E. TH9 skin-tropic autocrine paracrine capacity.Sci Transl 6: 219ra8Crossref TC17 constitutively skin33Naik 38Clark R.A. Resident memory disease.Sci 7: 269rv1Crossref squamous carcinomas39Roberts B.Y. Filler R.B. Lewis Glusac E.J. Hayday al.Characterizing tumor-promoting chemically carcinogenesis.Proc 2007; 104: 6770-6775Crossref (59) psoriatic plaques,40Cheuk Wikén Blomqvist L. Nylén Talme Ståhle al.Epidermal Th22 Tc17 form localized clinically healed 192: 3111-3120Crossref (227) suggesting contribute demonstration TH17-driven expression significantly Th17-related lesional nonlesional recent-onset potentially environmental commensals.41Brunner Israel Zhang Leonard Wen H.C. Huynh al.Early-onset TH2/TH17/TH22-centered lipid alterations.J 141: 2094-2106Abstract (139) 42Esaki Brunner Renert-Yuval Czarnowicki Tran TH2 TH17 polarized skin.J 1639-1651Abstract (240) Specificity limited cognate first description benefit came identification chemical moieties displayed interact TLR2 ligand, lipoteichoic acid, strain uniquely dampen inflammation.43Lai Di Nardo Leichtle Cogen Wu Z.R. receptor 3-dependent injury.Nat 5: 1377-1382Crossref (514) enhance defense enhancing peptide expression.44Lai Radek H.J. Macleod D.T. al.Activation small molecule produced increases against infections.J 130: 2211-2221Abstract (289) members genus envelope mycolic specifically IL-17A+ dermal γδ 2).45Ridaura V.K. Claesen Chen Y.E. Constantinides al.Contextual Corynebacterium.J Exp 215: 785-799Crossref By CD4+ programs broadly triggered wide array colonization.35Naik tempting speculate evolved sense complexity information rheostat continuously calibrate myriad elicited several contextual reinforcing Commensal-specific help heterologous protection pathogens. augmenting commensal-specific limit Candida albicans, establish infections.35Naik interac
Language: Английский
Citations
411Microorganisms, Journal Year: 2021, Volume and Issue: 9(2), P. 353 - 353
Published: Feb. 11, 2021
The microbiome plays an important role in a wide variety of skin disorders. Not only is the altered, but also surprisingly many diseases are accompanied by altered gut microbiome. key regulator for immune system, as it aims to maintain homeostasis communicating with tissues and organs bidirectional manner. Hence, dysbiosis and/or associated response, promoting development diseases, such atopic dermatitis, psoriasis, acne vulgaris, dandruff, even cancer. Here, we focus on associations between microbiome, diet, metabolites, responses pathologies. This review describes exhaustive list common conditions well current body evidence dysbiosis, dietary links, their interplay conditions. An enhanced understanding local including underlying mechanisms necessary shed light microbial involvement human develop new therapeutic approaches.
Language: Английский
Citations
393American Journal of Clinical Dermatology, Journal Year: 2019, Volume and Issue: 20(3), P. 335 - 344
Published: Jan. 10, 2019
Language: Английский
Citations
236Nature Medicine, Journal Year: 2021, Volume and Issue: 27(4), P. 700 - 709
Published: Feb. 22, 2021
Language: Английский
Citations
224Trends in Microbiology, Journal Year: 2019, Volume and Issue: 27(6), P. 497 - 507
Published: March 5, 2019
Language: Английский
Citations
211Protein & Cell, Journal Year: 2020, Volume and Issue: 12(5), P. 426 - 435
Published: Dec. 9, 2020
Abstract Although intestinal microbiome have been established as an important biomarker and regulator of cancer development therapeutic response, less is known about the role at other body sites in cancer. Emerging evidence has revealed that local microbiota make up part tumor microenvironment across many types cancer, especially cancers arising from mucosal sites, including lung, skin gastrointestinal tract. The populations bacteria reside specifically within tumors found to be tumor-type specific, mechanistic studies demonstrated tumor-associated may directly regulate initiation, progression responses chemo- or immuno-therapies. This review aims provide a comprehensive literature on cancerous tissue, their function mechanism action treatment.
Language: Английский
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203Nature Biotechnology, Journal Year: 2022, Volume and Issue: 40(8), P. 1259 - 1269
Published: March 17, 2022
Abstract Living bacteria therapies have been proposed as an alternative approach to treating a broad array of cancers. In this study, we developed genetically encoded microbial encapsulation system with tunable and dynamic expression surface capsular polysaccharides that enhances systemic delivery. Based on small RNA screen biosynthesis pathways, constructed inducible synthetic gene circuits regulate bacterial in Escherichia coli Nissle 1917. These are capable temporarily evading immune attack, whereas subsequent loss results effective clearance vivo. This delivery strategy enabled ten-fold increase maximum tolerated dose improved anti-tumor efficacy murine models cancer. Furthermore, situ increased the fraction translocation among mouse tumors, leading distal tumors. The programmable promises enhance therapeutic utility living engineered for
Language: Английский
Citations
175Microbiome, Journal Year: 2021, Volume and Issue: 9(1)
Published: May 30, 2021
Abstract The skin is the exterior interface of human body with environment. Despite its harsh physical landscape, colonized by diverse commensal microbes. In this review, we discuss recent insights into microbial populations, including their composition and role in health disease modulation intrinsic extrinsic factors, a focus on pathobiological basis aging. We also describe most tools for investigating microbiota microbe-skin relationships perspectives regarding challenges microbiome manipulation.
Language: Английский
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174Nature Reviews Microbiology, Journal Year: 2022, Volume and Issue: 21(2), P. 97 - 111
Published: Aug. 30, 2022
Language: Английский
Citations
165