Atopic dermatitis: a review of evolving targeted therapies

被引:13
作者
Kalamaha, Kadra [1 ]
Reis, Erin [1 ]
Newton, Shauna [1 ]
Roche, Conor [1 ]
Julson, Janet [1 ]
Fernandes, Hermina [1 ,2 ]
Rodrigues, Jonathan [1 ,3 ,4 ]
机构
[1] Univ North Dakota, Sch Med & Hlth Sci, Dept Internal Med, Bismarck, ND USA
[2] Sanford Hlth, Hematol & Med Oncol, Bismarck, ND USA
[3] Univ North Dakota, Sch Med & Hlth Sci, Dept Pediat, Bismarck, ND USA
[4] Sanford Hlth, Allergy & Immunol, 715 East Broadway Ave NE, Bismarck, ND 58501 USA
关键词
Atopic dermatitis; biologics; cytokines; eczema; immunomodulators; interleukin; monoclonal antibodies; THYMIC STROMAL LYMPHOPOIETIN; ANTI-CD20 RITUXIMAB TREATMENT; CYCLIC AMP-PHOSPHODIESTERASE; ANTI-IGE THERAPY; SKIN BARRIER; DOUBLE-BLIND; PATHOGENIC ROLE; ADULT PATIENTS; CASE SERIES; PPAR-GAMMA;
D O I
10.1080/1744666X.2019.1560267
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: Atopic dermatitis (AD) is a chronic inflammatory skin condition, affecting a significant number of patients of all ages. As we learn more about the pathogenesis of AD, new targeted treatment options are being developed to better tailor its management. Currently, a variety of biologic agents are utilized to target specific components and regulators of the inflammatory pathways in allergic and inflammatory conditions. These targeted therapies allow for greater efficacy while limiting adverse effects. Areas covered: This review examines the current literature in respect to several different monoclonal antibodies that are being studied toward a personalized approach in the treatment of AD. Expert opinion: Several trials examining the use of biologics for AD have demonstrated mixed success. While some have shown promise for improvement of clinical symptoms, there are several barriers to support consistent use including cost, adverse effects, small sample sizes, conflicting evidence, and lack of demonstrated long-term safety and efficacy. The ultimate goal for future research is to develop biomarkers for different AD phenotypes in order to allow for targeted therapy of AD.
引用
收藏
页码:275 / 288
页数:14
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