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Paradoxical skin lesions induced by anti-TNF-α agents in SAPHO syndrome

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Abstract

The objectives of the study were to characterize the clinical picture of paradoxical skin lesions in SAPHO patients treated with anti-TNF-α agents and to explore its pathogenesis. Patients treated with anti-TNF-α therapy were identified from a cohort of 164 SAPHO patients. The clinical data and skin biopsies were collected. The usage, efficacy, and side effects of anti-TNF-α therapy were recorded. Forty-one (25.0%) patients received anti-TNF-α therapy, of which seven (17.1%) developed paradoxical skin lesions after 1 to 14 infusions. Patients with such lesions were older at onset of skin lesions than those without (p = 0.034). Expression of TNF-α in palmoplantar pustulosis increased after anti-TNF-α therapy in the two examined patients with exacerbated skin lesions. Anti-TNF-α therapy induces paradoxical skin lesions in 17.1% SAPHO patients. Late onset of skin manifestations is associated with an increased risk of such lesions. The paradoxical elevation of TNF-α expression in lesions may contribute to this phenomenon.

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Funding

This study was supported by China National Natural Science Funds (No. 81371731) and the Capital Medical Research and Development Fund (No. 2016-4-40112), the Education Reform Projects of Peking Union Medical College (No. 2016zlgc0106), the CAMS Initiative for Innovative Medicine (No. 2017-I2M-3-001), and the National Key Research and Development Program of China (No. 2016YFC0901500).

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Correspondence to Li Li.

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The study was approved by the Ethics Committee of Peking Union Medical College Hospital, Peking Union Medical College, and Chinese Academy of Medical Sciences (ethics documents number ZS-944). All individual participants provided written informed consent to participate in this cohort at the time of inclusion.

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Li, C., Wu, X., Cao, Y. et al. Paradoxical skin lesions induced by anti-TNF-α agents in SAPHO syndrome. Clin Rheumatol 38, 53–61 (2019). https://doi.org/10.1007/s10067-018-4083-5

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  • DOI: https://doi.org/10.1007/s10067-018-4083-5

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