医学                        
                
                                
                        
                            胸腺基质淋巴细胞生成素                        
                
                                
                        
                            特应性皮炎                        
                
                                
                        
                            贾纳斯激酶                        
                
                                
                        
                            杜皮鲁玛                        
                
                                
                        
                            免疫失调                        
                
                                
                        
                            免疫学                        
                
                                
                        
                            免疫系统                        
                
                                
                        
                            细胞因子                        
                
                        
                    
            作者
            
                Kazuhiko Yamamura,Takeshi Nakahara            
         
                    
        
    
            
        
                
            摘要
            
            Atopic dermatitis (AD) is one of the most common chronic inflammatory skin diseases, and the condition is typified by barrier dysfunction and immune dysregulation. Recent studies have characterized various phenotypes and endotypes of AD and elucidated the mechanism. Numerous topical and systemic narrow targeting therapies for AD have been developed according to these findings. Topical medications, including Janus kinase (JAK) inhibitors, phosphodiesterase 4 inhibitors, and the aryl hydrocarbon receptor agonist tapinarof, are effective and safe for AD compared to topical corticosteroids. Oral JAK inhibitors and monoclonal antibodies targeting interleukin (IL)-4, IL-13, IL-31, IL-33, OX40, thymic stromal lymphopoietin, and sphingosine 1-phosphate signaling have displayed outstanding efficacy against moderate-to-severe AD. We are currently in a new era of AD treatment.
         
            
 
                 
                
                    
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