Atopic Dermatitis

A special issue of Medicina (ISSN 1648-9144). This special issue belongs to the section "Hematology and Immunology".

Deadline for manuscript submissions: closed (10 April 2022) | Viewed by 3247

Special Issue Editor


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Guest Editor
Department of Dermatology and Venereology, Faculty Hospital and Medical Faculty of Charles University, Hradec Králové, Czech Republic
Interests: skin tumors; atopic dermatitis

Special Issue Information

Dear Colleagues,

Atopic dermatitis is a chronic inflammatory skin disease characterized by inflammatory, chronically relapsing, and pruritic eczematous flares. With an increasing prevalence in recent decades, atopic dermatitis has become a global health issue. Due to the unpredictable disease course, its visible skin lesions, itching, and scratching followed by sleeplessness, other associated atopic diseases, and behavioral and psychiatric disorders, AD is an immense burden for patients and caregivers. It is almost always associated with IgE sensitization to airborne, food-derived, microbial allergens, and aeroallergens; however, non-IgE-mediated pathomechanisms also seem to be operative in atopic dermatitis, and it is often difficult to identify the disease-causing allergens. Molecular allergy diagnosis using single-plex allergens or multiplex allergen microarrays are typical methods of precision medicine. There is growing evidence that the use of molecular allergy diagnosis in combination with conventional sensitization testing improves analytical and diagnostic performance.

Atopic diseases appear to have a natural progression, with atopic dermatitis being the first to manifest, generally in infancy or childhood, followed by other atopic diseases, such as food allergy, allergic rhinitis, or allergic asthma. This natural progression of atopic diseases is termed the “Allergic March” or “Atopic March.” The presence of IgE antibodies, proinflammatory Th2-type cytokines, and the natural progression observed with atopic diseases has led some researchers to suggest that they are all different manifestations of the same disease.

Atopic dermatitis and food allergy have increased in prevalence in industrialized countries in recent decades and pose a significant health burden. Cow's milk, hen's egg, peanut, soy, wheat, fish, tree nuts, and shellfish are the most common food allergens.

Imbalance in the composition of skin microbiota facilitates the emergence and course of many skin diseases. In patients suffering from atopic dermatitis, this balance is disturbed mainly by the colonization of Staphylococcus aureus strains, which have a strong pro-inflammatory potential and are involved in the exacerbation of atopic dermatitis. The degree of colonization is correlated with the severity of the disease.

Articles explaining the pathophysiology and epidemiology of atopic dermatitis, as well as potential challenges facing its successful treatment, and articles dealing with the treatment of atopic dermatitis (emollients, topical corticosteroids, and topical calcineurin inhibitors; Janus kinase inhibitors; and biological treatment), are encouraged.

This Special Issue regarding the topic “Atopic dermatitis” shall serve as a comprehensive overview of currently available knowledge on atopic dermatitis.

Dear Authors, thank you very much for your contributions to these topics.

Dr. Jarmila Čelakovská
Guest Editor

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Keywords

  • atopic dermatitis
  • food allergy
  • therapy
  • epidemiology
  • pathophysiology

Published Papers (1 paper)

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Research

16 pages, 5976 KiB  
Article
Topical Application of Galgeunhwanggeumhwangryeon-Tang Recovers Skin-Lipid Barrier and Ameliorates Inflammation via Filaggrin-Thymic Stromal Lymphopoietin-Interleukin 4 Pathway
by Sang-Hyun Ahn, Su Shin, Yoonju Do, Yunju Jo, Dongryeol Ryu, Ki-Tae Ha and Kibong Kim
Medicina 2021, 57(12), 1387; https://0-doi-org.brum.beds.ac.uk/10.3390/medicina57121387 - 20 Dec 2021
Cited by 3 | Viewed by 2790
Abstract
Background and objectives: The purpose of this study was to confirm the effect of Galgeunhwanggeumhwangryeon-tang (GGRT) on the skin barrier integrity and inflammation in an atopic dermatitis-like animal model. Materials and Methods: The model was established using lipid barrier elimination (LBE) in BALB/c [...] Read more.
Background and objectives: The purpose of this study was to confirm the effect of Galgeunhwanggeumhwangryeon-tang (GGRT) on the skin barrier integrity and inflammation in an atopic dermatitis-like animal model. Materials and Methods: The model was established using lipid barrier elimination (LBE) in BALB/c mice. Ceramide 3B, a control drug, and GGRT were applied to the skin of LBE mice. Gross observation and histological examination were combined with measurement of skin score, trans-epidermal water loss, and pH. The expression of filaggrin, kallikrein-related peptidase 7 (KLK7), protease-activated receptor-2 (PAR-2), thymic stromal lymphopoietin (TSLP), and interleukin 4 (IL-4) was examined. Results: The effect of GGRT on atopic dermatitis was estimated in silico using two individual gene sets of human atopic dermatitis. In animal experiments, GGRT treatment reduced atopic dermatitis-like symptoms, as confirmed via gross and histological observations, skin score, pH change, and trans-epidermal water loss. The expression level of filaggrin increased in the skin of GGRT-treated mice compared to that in the LBE group. The expression levels of KLK7, PAR2, TSLP, and IL-4 were decreased in GGRT-treated mice skin compared to those in LBE mice. Conclusions: We demonstrated that GGRT restored the skin barrier and reduced inflammatory reactions in a murine model of atopic dermatitis. Full article
(This article belongs to the Special Issue Atopic Dermatitis)
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