AUTHOR=Liu Ben , Wu Yibei , Wu Xiaoyan , Zhong Xinyu , Xue Ruzeng , Zhang Zhenying 

TITLE=Dupilumab improve acquired reactive perforating collagenosis characterized by type 2 inflammation

JOURNAL=Frontiers in Immunology

VOLUME=14

YEAR=2023

URL=https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2023.1240262

DOI=10.3389/fimmu.2023.1240262

ISSN=1664-3224

ABSTRACT=<sec><title>Background</title><p>Acquired reactive perforating collagenosis (ARPC) is a clinically challenging disease with an unclear pathogenesis.</p></sec><sec><title>Objective</title><p>To evaluate the efficacy and safety of dupilumab for the treatment of ARPC, and analyze the expression of type 2 inflammation-related molecules in ARPC lesions.</p></sec><sec><title>Methods</title><p>This retrospective cohort study included 20 patients with ARPC; 10 received dupilumab and 10 received conventional therapy. The efficacy and safety of dupilumab were evaluated at 12 weeks. Immunohistochemical and immunofluorescence analyses of T- and B-cell markers, and type 2 inflammation-related cytokines, were performed on skin samples from ARPC patients, atopic dermatitis (AD) patients, and healthy controls.</p></sec><sec><title>Results</title><p>Significantly more patients showed improvements in the Investigator Global Assessment score (100% vs. 0%; p &lt; 0.0001) and itching (90%/8.33%, P =.001) in the dupilumab group compared to the conventional group at 12 weeks. There were no adverse effects in the dupilumab group. The ARPC lesions showed enhanced dermal infiltration of CD3+ T-cells, with a predominance of Th2 cells, similar to AD lesions. IL-4 and IL-13 were co-localized with GATA3 in ARPC lesions.</p></sec><sec><title>Conclusion</title><p>Dupilumab improved ARPC charaterized with type 2 inflammation.</p></sec>