Gallagher Kennedy, Halperin-Goldstein Sofia, Paller Amy S
Department of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Department of Medicine/Allergy and Immunology, Northwestern University Feinberg School of Medicine, Chicago, Illinois; Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Ann Allergy Asthma Immunol. 2025 Jun 23. doi: 10.1016/j.anai.2025.06.020.
This review evaluates the efficacy and safety of novel and emerging topical and systemic therapies for atopic dermatitis across pediatric and adult populations with an emphasis on recent advancements and future directions. Data were sourced from peer-reviewed publications (PubMed), scientific meeting abstracts, ClinicalTrials.gov, and industry press releases. Several new agents have received Food and Drug Administration approval, expanding therapeutic options for patients. Nonsteroidal topical treatments, such as roflumilast and tapinarof creams, are approved for adults and for children down to 6 and 2 years, respectively. Topical Janus kinase (JAK) inhibitors, including ruxolitinib, leverage inhibition of the JAK1 pathway with low concern for toxicity. The use of biologics targeting the interleukin (IL)-4/IL-13 pathway has expanded; dupilumab is approved for patients aged 6 months and older, and tralokinumab and lebrikizumab are approved for those aged 12 years and older. Most recently, nemolizumab, targeting the IL-31 receptor, which mediates nonhistaminergic itch, has been approved for patients 12 years and older. Although baricitinib is approved in Europe and Japan, upadacitinib and abrocitinib remain the only oral JAK inhibitors approved for patients 12 years and older in the United States. Promising investigational therapies, particularly through topically altering the microbiome (bacteriotherapy) and systemic agents targeting the OX40/OX40L pathway and multispecific antibodies, are in development. These innovations represent a shift toward personalized atopic dermatitis management. As the treatment landscape evolves, ongoing research is essential to assess long-term safety and efficacy, and to develop predictive models that optimize treatment strategies, ultimately improving patient outcomes and quality of life.
本综述评估了针对儿童和成人特应性皮炎的新型及新兴局部和全身疗法的疗效和安全性,重点关注近期进展和未来方向。数据来源包括同行评审出版物(PubMed)、科学会议摘要、ClinicalTrials.gov和行业新闻稿。几种新药物已获得美国食品药品监督管理局批准,为患者扩大了治疗选择。非甾体局部治疗药物,如罗氟司特和他扎罗汀乳膏,分别被批准用于成人以及6岁和2岁以上儿童。局部Janus激酶(JAK)抑制剂,包括芦可替尼,通过抑制JAK1途径发挥作用,且毒性较低。靶向白细胞介素(IL)-4/IL-13途径的生物制剂的应用有所扩展;度普利尤单抗被批准用于6个月及以上患者,曲罗芦单抗和瑞莎珠单抗被批准用于12岁及以上患者。最近,靶向介导非组胺能瘙痒的IL-31受体的奈莫利单抗已被批准用于12岁及以上患者。尽管巴瑞替尼在欧洲和日本已获批准,但在美国,乌帕替尼和阿布昔替尼仍是仅有的被批准用于12岁及以上患者的口服JAK抑制剂。有前景的研究性疗法,特别是通过局部改变微生物群(细菌疗法)以及靶向OX40/OX40L途径的全身药物和多特异性抗体,正在研发中。这些创新代表了特应性皮炎管理向个性化的转变。随着治疗格局的演变,持续研究对于评估长期安全性和疗效以及开发优化治疗策略的预测模型至关重要,最终改善患者预后和生活质量。