4.5 Article

Treatment of bullous pemphigoid with dupilumab: Dupilumab exerts its effect by primarily suppressing T-helper 2 cytokines

期刊

JOURNAL OF DERMATOLOGY
卷 49, 期 9, 页码 845-850

出版社

WILEY
DOI: 10.1111/1346-8138.16428

关键词

bullous pemphigoid; cytokines; dupilumab; interleukin 13; interleukin 4; T-helper 2

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Investigated the dynamics of cytokine-producing T cells before and after treatment in a patient with bullous pemphigoid (BP), and found that Th2 cells are involved in the pathogenesis of BP, and dupilumab exerts its effect mainly by suppressing Th2 cytokines.
We report a patient with bullous pemphigoid (BP) who was successfully treated with dupilumab monotherapy. To clarify the underlying mechanism of this effective treatment, we investigated the dynamics of a variety of cytokine-producing T cells before and after treatment in the circulation and in blister fluid using flow cytometry. The patient was a 72-year-old woman who had a pruritic eruption consisting of erythema and tense blisters on the whole body. The skin biopsy and direct immunofluorescence of the skin were typical for BP. The serum level of anti-BP180NC16a antibodies was 111 U/ml. Flow cytometric analyses revealed that the proportions of circulating interleukin (IL)-4-, IL-13-, and IL-31-producing CD4(+) and CD8(+) T cells were substantially higher in our BP patient than in healthy subjects. Moreover, IL-4- and IL-13-producing CD4(+) and CD8(+) T cells were much higher in the blister fluids than in the circulation, whereas IL-31-producing CD4(+) and CD8(+) T cells were only slightly higher in the blister fluids. The proportions of circulating interferon (IFN)-gamma-producing CD4(+) and CD8(+) T cells in the circulation were slightly lower in the patient than in healthy subjects. There was no significant difference in the circulating IL-17-producing CD4(+) and CD8(+) T cells between the patient and healthy subjects, although IL-17-producing CD4(+) and CD8(+) T cells were slightly higher in the blister fluids. Treatment with dupilumab promptly improved the pruritus and skin lesions, and anti-BP180 antibodies became negative. After treatment with dupilumab, the proportions of circulating IL-4- and IL-13-producing CD4(+) T cells mainly decreased and IL-17- and IL-31-producing CD4(+) T cells slightly decreased. There were no significant differences in the proportions of circulating IFN-gamma-producing CD4(+) and CD8(+) T cells between before and after treatment. These results suggest that T-helper (Th)2 cells are involved in the pathogenesis of BP, and dupilumab exerts its effect mainly by suppressing Th2 cytokines.

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