Zusammenfassung
Hintergrund
Die Psoriasis ist eine häufige systemische und chronische Entzündungskrankheit. Das Mikrobiom spielt bei ihrer Entstehung und Verlauf eine zunehmend wichtige Rolle.
Ziel der Arbeit
Dargestellt werden sollten die Rolle des Mikrobioms bei Psoriasis, gängige Nachweismethoden und potenzielle Anwendungsmöglichkeiten.
Material und Methoden
Es erfolgten eine Literaturrecherche in den Datenbanken von Medline und PubMed sowie eine allgemeine Internetrecherche und die Auseinandersetzung mit Buchquellen.
Ergebnisse
Sowohl das Haut- als auch das Darmmikrobiom können die Entstehung und den Verlauf der Psoriasis modulieren. Eine Verbindung zwischen dem Mikrobiom und immunologischen Mechanismen stellen antimikrobielle Peptide dar, die das Mikrobiom an Grenzflächen regulieren und als Antigen die Psoriasis triggern können. Um das Mikrobiom eines Patienten zu analysieren, stehen inzwischen effiziente Verfahren zur Verfügung, etwa das „16S rRNA next-generation sequencing“.
Diskussion
Die Analyse des Mikrobioms bei Psoriasispatienten vor- und unter/nach einer Therapie stellt die Grundlage zur Identifikation potenzieller Biomarker dar, die zur Weiterentwicklung einer personalisierten Medizin verwendet werden können.
Abstract
Background
Psoriasis is a frequent chronic inflammatory systemic disease. It is associated with changes in the microbiome, which may trigger psoriasis and influence the course of the disease.
Objective
Current methods for detection and the potential role of the microbiome in the pathogenesis of psoriasis are described.
Material and methods
A literature search was conducted using the databases Medline and PubMed as well as a general internet and book research.
Results
Both skin and gut microbiota are involved in the immunopathogenesis and may substantially modulate psoriasis. Antimicrobial peptides may serve as a link between the microbiome and the immunological mechanisms in psoriasis by regulating the microbiome at interfaces and can trigger psoriasis as antigens. Recent innovative methods, such as 16S rRNA next-generation sequencing significantly facilitate microbiome analysis.
Conclusion
The analysis of the microbiome in patients with psoriasis before, during and after treatment provides a basis for the identification of potential biomarkers for predicting individual treatment responses and facilitating the decision for a certain treatment.
Literatur
Alekseyenko AV, Perez-Perez GI, De Souza A et al (2013) Community differentiation of the cutaneous microbiota in psoriasis. Microbiome 1:31. https://doi.org/10.1186/2049-2618-1-31
Baquerizo Nole KL, Yim E, Keri JE (2014) Probiotics and prebiotics in dermatology. J Am Acad Dermatol 71:814–821. https://doi.org/10.1016/j.jaad.2014.04.050
Bartenjev I, Rogl Butina M, Potocnik M (2000) Subclinical microbial infection in patients with chronic plaque psoriasis. Acta Derm Venereol Suppl (Stockh). https://doi.org/10.1080/00015550050500068
Caporaso JG, Kuczynski J, Stombaugh J et al (2010) QIIME allows analysis of high-throughput community sequencing data. Nat Methods 7:335–336. https://doi.org/10.1038/nmeth.f.303
Christensen GJM, Brüggemann H (2014) Bacterial skin commensals and their role as host guardians. Benef Microbes 5:201–215. https://doi.org/10.3920/BM2012.0062
Codoñer FM, Ramírez-Bosca A, Climent E et al (2018) Gut microbial composition in patients with psoriasis. Sci Rep 8:3812. https://doi.org/10.1038/s41598-018-22125-y
Eppinga H, Sperna Weiland CJ, Thio HB et al (2016) Similar depletion of protective Faecalibacterium prausnitzii in psoriasis and inflammatory bowel disease, but not in hidradenitis suppurativa. J Crohns Colitis 10:1067–1075. https://doi.org/10.1093/ecco-jcc/jjw070
Fahlén A, Engstrand L, Baker BS et al (2012) Comparison of bacterial microbiota in skin biopsies from normal and psoriatic skin. Arch Dermatol Res 304:15–22. https://doi.org/10.1007/s00403-011-1189-x
Fry L, Baker BS (2007) Triggering psoriasis: The role of infections and medications. Clin Dermatol 25:606–615. https://doi.org/10.1016/j.clindermatol.2007.08.015
Gao Z, Tseng C, Pei Z, Blaser MJ (2007) Molecular analysis of human forearm superficial skin bacterial biota. Proc Natl Acad Sci U S A 104:2927–2932. https://doi.org/10.1073/pnas.0607077104
Gao Z, Tseng C, Strober BE et al (2008) Substantial alterations of the cutaneous bacterial biota in psoriatic lesions. PLoS ONE 3:e2719. https://doi.org/10.1371/journal.pone.0002719
Harder J, Bartels J, Christophers E, Schröder JM (2001) Isolation and characterization of human beta -defensin-3, a novel human inducible peptide antibiotic. J Biol Chem 276:5707–5713. https://doi.org/10.1074/jbc.M008557200
Harder J, Schröder J‑M (2005) Psoriatic scales: A promising source for the isolation of human skin-derived antimicrobial proteins. J Leukoc Biol 77:476–486. https://doi.org/10.1189/jlb.0704409
Hiippala K, Jouhten H, Ronkainen A et al (2018) The potential of gut commensals in reinforcing intestinal barrier function and alleviating inflammation. Nutrients. https://doi.org/10.3390/nu10080988
Human Microbiome Project Consortium (2012) Structure, function and diversity of the healthy human microbiome. Nature 486:207–214. https://doi.org/10.1038/nature11234
Loesche MA, Farahi K, Capone K et al (2018) Longitudinal study of the psoriasis-associated skin microbiome during therapy with ustekinumab in a randomized phase 3b clinical trial. J Invest Dermatol 138:1973–1981. https://doi.org/10.1016/j.jid.2018.03.1501
López-García B, Lee PHA, Gallo RL (2006) Expression and potential function of cathelicidin antimicrobial peptides in dermatophytosis and tinea versicolor. J Antimicrob Chemother 57:877–882. https://doi.org/10.1093/jac/dkl078
Martin R, Henley JB, Sarrazin P, Seité S (2015) Skin microbiome in patients with psoriasis before and after balneotherapy at the thermal care center of la Roche-Posay. J Drugs Dermatol 14:1400–1405
Mosca A, Leclerc M, Hugot JP (2016) Gut microbiota diversity and human diseases: Should we reintroduce key predators in our ecosystem? Front Microbiol 7:455. https://doi.org/10.3389/fmicb.2016.00455
Navid F, Boniotto M, Walker C et al (2012) Induction of regulatory T cells by a murine β‑defensin. J Immunol 1950(188):735–743. https://doi.org/10.4049/jimmunol.1100452
Norrlind R (1955) The significance of infections in the origination of psoriasis. Acta Rheumatol Scand 1:135–144
Ong PY, Ohtake T, Brandt C et al (2002) Endogenous antimicrobial peptides and skin infections in atopic dermatitis. N Engl J Med 347:1151–1160. https://doi.org/10.1056/NEJMoa021481
Rosenberg EW, Belew PW (1982) Improvement of psoriasis of the scalp with ketoconazole. Arch Dermatol 118:370–371
Scher JU, Ubeda C, Artacho A et al (2015) Decreased bacterial diversity characterizes the altered gut microbiota in patients with psoriatic arthritis, resembling dysbiosis in inflammatory bowel disease. Arthritis Rheumatol 67:128–139. https://doi.org/10.1002/art.38892
Schloss PD, Westcott SL, Ryabin T et al (2009) Introducing mothur: Open-source, platform-independent, community-supported software for describing and comparing microbial communities. Appl Environ Microbiol 75:7537–7541. https://doi.org/10.1128/AEM.01541-09
Stehlikova Z, Kostovcikova K, Kverka M et al (2019) Crucial role of microbiota in experimental psoriasis revealed by a gnotobiotic mouse model. Front Microbiol. https://doi.org/10.3389/fmicb.2019.00236
Tervaert WC, Esseveld H (1970) A study of the incidence of haemolytic streptococci in the throat in patients with psoriasis vulgaris, with reference to their role in the pathogenesis of this disease. Dermatologica 140:282–290
Vijayashankar M, Raghunath N (2012) Pustular psoriasis responding to probiotics—A new insight. Our Dermatol Online 3:326–329. https://doi.org/10.7241/ourd.20124.71
Whyte HJ, Baughman RD (1964) Acute guttate psoriasis and streptococcal infection. Arch Dermatol 89:350–356
Winfield JM (1916) Psoriasis as a sequel to acute inflammations of the tonsils: A clinical note. J Cutan Dis 34:441–443
Wingens M, van Bergen BH, Hiemstra PS et al (1998) Induction of SLPI (ALP/HUSI-I) in epidermal keratinocytes. J Invest Dermatol 111:996–1002. https://doi.org/10.1046/j.1523-1747.1998.00425.x
Zeeuwen PLJM, Boekhorst J, Ederveen THA et al (2017) Reply to Meisel et al. J Invest Dermatol 137:961–962. https://doi.org/10.1016/j.jid.2016.11.013
Zhou Y, Xu ZZ, He Y et al (2018) Gut microbiota offers universal biomarkers across ethnicity in inflammatory bowel disease diagnosis and Infliximab response prediction. mSystems. https://doi.org/10.1128/mSystems.00188-17
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Interessenkonflikt
D. Thaçi: Prüfarzt/klinische Studien: Abbvie, Almiral, Amgen, Biogen-Idec, Bioskin, Boehringer-Ingelheim, BMS, Celgene, Chugai, Dermira, Dignity, Elli-Lilly, Forward-Pharma, Glaxo-Smith-Kline, Leo-Pharma, Janssen-Cilag, Maruho, Medac, MSD, Mitsubishi Pharma, Novartis, Pfizer, Regeneron, Roche, Sanofi, Sandoz-Hexal, UCB. Wissenschaftliche Vorträge unterstützt von: AbbVie, Almiral, BMS, Celgene, Janssen, Leo-Pharma, Lilly, La Roche-Possay, Novartis, MSD, Medac, Pfizer, Regeneron, Sanofi, Sandoz-Hexal, UCB. Mitglied des wissenschaftlichen Boards: AbbVie, Amgen, BMS, Celgene, Dignity, Eli-Lilly, Galapagos, Leo-Pharma, Janssen-Cilag, Morphosis, Novartis, Pfizer, MSD, Sandoz, Sanofi, UCB. M. Witte gibt an, dass kein Interessenkonflikt besteht.
Für diesen Beitrag wurden von den Autoren keine Studien an Menschen oder Tieren durchgeführt. Für die aufgeführten Studien gelten die jeweils dort angegebenen ethischen Richtlinien.
Rights and permissions
About this article
Cite this article
Witte, M., Thaçi, D. Psoriasis und Mikrobiom. Hautarzt 70, 416–421 (2019). https://doi.org/10.1007/s00105-019-4415-7
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00105-019-4415-7