کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5521179 1401252 2017 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
ReviewGene-to-screenChemokine neutralization as an innovative therapeutic strategy for atopic dermatitis
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیوتکنولوژی یا زیست‌فناوری
پیش نمایش صفحه اول مقاله
ReviewGene-to-screenChemokine neutralization as an innovative therapeutic strategy for atopic dermatitis
چکیده انگلیسی


- Atopic dermatitis is a major public health problem with unmet medical needs.
- Chemokines and their receptors are key players in atopic dermatitis.
- Chemokines form an intricate network with redundancy in ligands and receptors.
- Neutralization of specific chemokines is an innovative approach in this context.
- 'Neutraligands' could help to mitigate the symptoms of the disease.

Atopic dermatitis is a chronic inflammatory skin disease with no specific treatment, affecting 15-30% of children and 2-10% of adults in developed countries. Current therapies alleviate symptoms and include emollients, glucocorticoids and calcineurin inhibitors. The limited efficiency and side-effects of these medicines call for better treatment, and a cure for atopic dermatitis represents an unmet medical need. The chemokine/chemokine-receptor network constitutes an attractive target for drugs in atopic dermatitis. However, the highly intricate nature of the chemokine network makes it difficult to identify a clear receptor to target. After a short description of atopic dermatitis and its current therapies, this review presents the current knowledge of the chemokine/chemokine-receptor system role in the regulation of inflammatory cell recruitment into the skin. We discuss the limitations of classical chemokine receptor blockade and introduce the concept of neutralization of chemokine ligands. This strategy represents a potential breakthrough in developing therapeutic agents to treat atopic diseases.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Drug Discovery Today - Volume 22, Issue 4, April 2017, Pages 702-711
نویسندگان
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