The clinical efficacy and safety of anti-IgE therapy in recessive dystrophic epidermolysis bullosa

被引:7
作者
Chen, Fuying [1 ,2 ]
Guo, Yifeng [1 ,2 ]
Zhou, Kaili [1 ,2 ]
Deng, Dan [1 ,2 ]
Yue, Wanbo [1 ,2 ]
Yang, Weiqin [1 ]
Zhang, Beibei [1 ]
Li, Yue [1 ,2 ]
Liang, Jianying [1 ,2 ]
Li, Ming [1 ,2 ]
Yao, Zhirong [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Xinhua Hosp, Dept Dermatol, Sch Med, 1665 Kongjiang Rd, Shanghai 200092, Peoples R China
[2] Shanghai Jiao Tong Univ, Inst Dermatol, Sch Med, Shanghai, Peoples R China
关键词
anti-IgE; biologics; Omalizumab; recessive dystrophic epidermolysis bullosa; wound healing; COLLAGEN;
D O I
10.1111/cge.14062
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The treatment of recessive dystrophic epidermolysis bullosa (RDEB) remains challenging. Elevated IgE levels have previously been reported in several RDEB patients. In this prospective, single-centre, open intervention study, elevated IgE levels were seen in 11 out of 12 patients with intense pruritus, and the patients with elevated IgE levels received anti-IgE therapy every 4 weeks for at least three cycles. Compared with the baseline, 10 patients with RDEB had good clinical outcomes with enhanced wound healing, a reduction in Birmingham (epidermolysis bullosa) EB severity score by 15%, a reduction in affected body surface area by 23.3%, amelioration of skin inflammation, and an increase in type VII collagen deposition by 13.1-fold. All the patients had a good tolerance to anti-IgE therapy. Furthermore, patients with higher IgE levels tended to have higher disease severity and more favorable clinical outcomes. Our report also suggested the potential role of IgE in the pathogenesis of inflammatory conditions associated with RDEB. (ChiCTR1900021437).
引用
收藏
页码:110 / 115
页数:6
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