期刊
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
卷 135, 期 2, 页码 324-336出版社
MOSBY-ELSEVIER
DOI: 10.1016/j.jaci.2014.11.015
关键词
Psoriasis; atopic dermatitis; eczema; biologics; IL-23; T(H)17; T(H)2; T(H)22
资金
- Amgen
- Innovaderm
- Kyowa
- Serono
- Biogen Idec
- Delenex
- AbbVie
- Sanofi
- Baxter
- Xenoport
- Kineta
- Novartis
- Pfizer
- Janssen
- Lilly
- Merck
- Kadmon
- Dermira
- Boehringer
- BMS
- Paraxel
- Regeneron
- Sanofi Aventis
- MedImmune
- Celgene
- Steifel/GlaxoSmithKline
- Celsus
- Drais
Psoriasis and atopic dermatitis (AD) are common inflammatory skin diseases characterized by immune-mediated inflammation and abnormal keratinocyte differentiation. Although T-cell infiltration characterizes both diseases, T-cell polarization differs. Psoriasis is currently the best model for translational medicine because many targeted therapeutics have been developed and testing of targeted therapeutics has cemented psoriasis as IL-23/T(H)17 polarized. In patients with AD, although therapeutic development is approximately a decade behind that in patients with psoriasis, there is now active development and testing of targeted therapeutics against various immune axes (T(H)2, T(H)22, and IL-23/T(H)17). These clinical trials and subsequent molecular analyses using human samples will be able to clarify the relative roles of polar cytokines in patients with AD.
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