Swen Malte John
University of Osnabrück
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Publication
Featured researches published by Swen Malte John.
Contact Dermatitis | 2015
Jeanne Duus Johansen; Kristiina Aalto-Korte; Tove Agner; Klaus Ejner Andersen; Andreas J. Bircher; Magnus Bruze; Alicia Cannavó; Ana Giménez-Arnau; Margarida Gonçalo; An Goossens; Swen Malte John; Carola Lidén; Magnus Lindberg; Vera Mahler; Mihaly Matura; Thomas Rustemeyer; Jørgen Serup; Radoslaw Spiewak; Jacob P. Thyssen; Martine Vigan; Ian R. White; Mark Wilkinson; Wolfgang Uter
The present guideline summarizes all aspects of patch testing for the diagnosis of contact allergy in patients suspected of suffering, or having been suffering, from allergic contact dermatitis or other delayed‐type hypersensitivity skin and mucosal conditions. Sections with brief descriptions and discussions of different pertinent topics are followed by a highlighted short practical recommendation. Topics comprise, after an introduction with important definitions, materials, technique, modifications of epicutaneous testing, individual factors influencing the patch test outcome or necessitating special considerations, children, patients with occupational contact dermatitis and drug eruptions as special groups, patch testing of materials brought in by the patient, adverse effects of patch testing, and the final evaluation and patient counselling based on this judgement. Finally, short reference is made to aspects of (continuing) medical education and to electronic collection of data for epidemiological surveillance.
British Journal of Dermatology | 2008
C.M. de Jongh; Liubov Khrenova; Maarten M. Verberk; F. Calkoen; F. J. H. van Dijk; H. Voss; Swen Malte John; Sanja Kezic
Background Polymorphisms in the filaggrin (FLG) gene, which result in loss of filaggrin production, may alter the skin barrier and are a well‐known predisposing factor for atopic dermatitis.
Nutrition Journal | 2013
Bodo C. Melnik; Swen Malte John; Gerd Schmitz
Milk has been recognized to represent a functionally active nutrient system promoting neonatal growth of mammals. Cell growth is regulated by the nutrient-sensitive kinase mechanistic target of rapamycin complex 1 (mTORC1). There is still a lack of information on the mechanisms of mTORC1 up-regulation by milk consumption. This review presents milk as a materno-neonatal relay system functioning by transfer of preferential amino acids, which increase plasma levels of glucose-dependent insulinotropic polypeptide (GIP), glucagon-like peptide-1 (GLP-1), insulin, growth hormone (GH) and insulin-like growth factor-1 (IGF-1) for mTORC1 activation. Importantly, milk exosomes, which regularly contain microRNA-21, most likely represent a genetic transfection system enhancing mTORC1-driven metabolic processes. Whereas human breast milk is the ideal food for infants allowing appropriate postnatal growth and species-specific metabolic programming, persistent high milk signaling during adolescence and adulthood by continued cow´s milk consumption may promote mTORC1-driven diseases of civilization.
Journal of Translational Medicine | 2014
Bodo C. Melnik; Swen Malte John; Gerd Schmitz
Epidemiological evidence confirmed that raw cow’s milk consumption in the first year of life protects against the development of atopic diseases and increases the number of regulatory T-cells (Tregs). However, milk’s atopy-protective mode of action remains elusive.This review supported by translational research proposes that milk-derived microRNAs (miRs) may represent the missing candidates that promote long-term lineage commitment of Tregs downregulating IL-4/Th2-mediated atopic sensitization and effector immune responses. Milk transfers exosomal miRs including the ancient miR-155, which is important for the development of the immune system and controls pivotal target genes involved in the regulation of FoxP3 expression, IL-4 signaling, immunoglobulin class switching to IgE and FcϵRI expression. Boiling of milk abolishes milk’s exosomal miR-mediated bioactivity. Infant formula in comparison to human breast- or cow’s milk is deficient in bioactive exosomal miRs that may impair FoxP3 expression. The boost of milk-mediated miR may induce pivotal immunoregulatory and epigenetic modifications required for long-term thymic Treg lineage commitment explaining the atopy-protective effect of raw cow’s milk consumption.The presented concept offers a new option for the prevention of atopic diseases by the addition of physiological amounts of miR-155-enriched exosomes to infant formula for mothers incapable of breastfeeding.
Nutrition & Metabolism | 2011
Bodo C. Melnik; Swen Malte John; Gerd Schmitz
The insulin/insulin-like growth factor-1 (IGF-1) pathway drives an evolutionarily conserved network that regulates lifespan and longevity. Individuals with Laron syndrome who carry mutations in the growth hormone receptor (GHR) gene that lead to severe congenital IGF-1 deficiency with decreased insulin/IGF-1 signaling (IIS) exhibit reduced prevalence rates of acne, diabetes and cancer. Western diet with high intake of hyperglycemic carbohydrates and insulinotropic dairy over-stimulates IIS. The reduction of IIS in Laron subjects unmasks the potential role of persistent hyperactive IIS mediated by Western diet in the development of diseases of civilization and offers a rational perspective for dietary adjustments with less insulinotropic diets like the Paleolithic diet.
British Journal of Dermatology | 2013
Maaike J. Visser; L. Landeck; Linda E. Campbell; W.H.I. McLean; S. Weidinger; F. Calkoen; Swen Malte John; Sanja Kezic
Background Atopic dermatitis (AD) and loss‐of‐function mutations in the filaggrin gene (FLG) are both associated with chronic irritant contact dermatitis (ICD). As FLG mutations also are a major risk factor for AD, it is not clear whether FLG mutations are an independent risk factor for ICD or whether the risk is mediated by AD.
Skin Research and Technology | 2013
Johan L. Du Plessis; Aleksandr B. Stefaniak; F.C. Eloff; Swen Malte John; Tove Agner; Tzu-Chieh Chou; Rosemary Nixon; Markus Steiner; Anja Franken; Irena Kudla; Linn Holness
There is an emerging perspective that it is not sufficient to just assess skin exposure to physical and chemical stressors in workplaces, but that it is also important to assess the condition, i.e. skin barrier function of the exposed skin at the time of exposure. The workplace environment, representing a non‐clinical environment, can be highly variable and difficult to control, thereby presenting unique measurement challenges not typically encountered in clinical settings.
Contact Dermatitis | 2008
Cindy M. De Jongh; Swen Malte John; Derk P. Bruynzeel; F. Calkoen; Frank J. H. van Dijk; Liubov Khrenova; Thomas Rustemeyer; Maarten M. Verberk; Sanja Kezic
Background: Cytokines play an important role in skin inflammation.
British Journal of Dermatology | 2009
N. Stutz; Detlef Becker; Uta Jappe; Swen Malte John; A. Ladwig; Petra Spornraft-Ragaller; Wolfgang Uter; H. Löffler
Background Nurses have a high risk of developing hand eczema due to hand disinfection procedures.
Contact Dermatitis | 2013
Elke Weisshaar; Christoph Skudlik; Reginald Scheidt; Uwe Matterne; Britta Wulfhorst; Michael Schönfeld; Peter Elsner; Thomas L. Diepgen; Swen Malte John
Background. Occupational skin disease (OSD) is common, and imposes a considerable personal and public burden. To tackle OSD, the German stepwise procedure of handling OSD was set up. It contains an interdisciplinary, integrated inpatient rehabilitation measure [tertiary individual prevention (TIP)] [dermatological treatment and diagnostic procedures, and patient education (health and psychological)]. The primary aims of the TIP are reduction of the severity of OSD, reduction in the use of corticosteroids, facilitation of return to work, decreased absence from work, and enhanced quality of life (QoL). It was positively evaluated for a period of 4 weeks after return to work.