TY - JOUR
T1 - Biologics for chronic inflammatory skin diseases
T2 - an update for the clinician
AU - Yao, Yiqiu
AU - Ravn Jørgensen, Astrid-Helene
AU - Thomsen, Simon Francis
PY - 2020/2/17
Y1 - 2020/2/17
N2 - The introduction and continuous development in biological drugs has greatly improved the therapeutic quality for patients with chronic inflammatory skin conditions. Current approaches to the biologic treatment of psoriasis, atopic dermatitis, chronic spontaneous urticaria, and hidradenitis suppurativa include licensed use of traditional antitumor necrosis factor agents, selective interleukin antagonists (IL-4, IL-12/23, IL-17), and the IgE inhibitor omalizumab, and as the knowledge on the pathogenesis of these diseases expands, off-label uses of the currently available biologics are becoming increasingly attractive, and the number of investigational drugs is growing progressively plentiful. In recent years, small molecule inhibitors, many of which are used in cancer therapy, have emerged as valuable future prospects in the treatment of inflammatory diseases. Inhibitors of PGD2, JAK, Syk, and C5a all have, to some extent, theorized efficacy in the treatment of chronic skin conditions, and multiple clinical trials are ongoing. The extensive research of the novel targets' roles in the pathogenesis of dermatological conditions should, in the future, further improve the therapeutic options for both the patients and physicians involved.
AB - The introduction and continuous development in biological drugs has greatly improved the therapeutic quality for patients with chronic inflammatory skin conditions. Current approaches to the biologic treatment of psoriasis, atopic dermatitis, chronic spontaneous urticaria, and hidradenitis suppurativa include licensed use of traditional antitumor necrosis factor agents, selective interleukin antagonists (IL-4, IL-12/23, IL-17), and the IgE inhibitor omalizumab, and as the knowledge on the pathogenesis of these diseases expands, off-label uses of the currently available biologics are becoming increasingly attractive, and the number of investigational drugs is growing progressively plentiful. In recent years, small molecule inhibitors, many of which are used in cancer therapy, have emerged as valuable future prospects in the treatment of inflammatory diseases. Inhibitors of PGD2, JAK, Syk, and C5a all have, to some extent, theorized efficacy in the treatment of chronic skin conditions, and multiple clinical trials are ongoing. The extensive research of the novel targets' roles in the pathogenesis of dermatological conditions should, in the future, further improve the therapeutic options for both the patients and physicians involved.
KW - Antibodies, Monoclonal/therapeutic use
KW - Biological Products/therapeutic use
KW - Dermatitis, Atopic/drug therapy
KW - Dermatologic Agents/therapeutic use
KW - Etanercept/therapeutic use
KW - Hidradenitis Suppurativa/drug therapy
KW - Humans
KW - Psoriasis/drug therapy
KW - Skin Diseases/drug therapy
KW - Small Molecule Libraries/therapeutic use
KW - chronic urticaria
KW - atopic dermatitis
KW - hidradenitis suppurativa
KW - Biologics
KW - psoriasis
KW - small molecules
UR - http://www.scopus.com/inward/record.url?scp=85063370566&partnerID=8YFLogxK
U2 - 10.1080/09546634.2019.1589643
DO - 10.1080/09546634.2019.1589643
M3 - Review
C2 - 30827126
SN - 0954-6634
VL - 31
SP - 108
EP - 130
JO - The Journal of dermatological treatment
JF - The Journal of dermatological treatment
IS - 2
ER -