Association of Hidradenitis Suppurativa With T Helper 1/T Helper 17 Phenotypes: A Semantic Map Analysis
IMPORTANCE: In spite of progress in understanding the mechanisms underlying hidradenitis suppurativa (HS) as an inflammatory skin disease, there is still a demand for an overview on immunopathogenesis of HS. OBJECTIVE: To demonstrate the importance of the type 1/type 17 immune response in lesional H...
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Veröffentlicht in: | JAMA dermatology (Chicago, Ill.) Ill.), 2018-05, Vol.154 (5), p.592-595 |
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Zusammenfassung: | IMPORTANCE: In spite of progress in understanding the mechanisms underlying hidradenitis suppurativa (HS) as an inflammatory skin disease, there is still a demand for an overview on immunopathogenesis of HS. OBJECTIVE: To demonstrate the importance of the type 1/type 17 immune response in lesional HS skin by drawing a semantic connectivity map. DESIGN, SETTING, AND PARTICIPANTS: Single-center case series of 24 patients with HS. Association of HS with T helper 1/T helper 17 (TH1/TH17) phenotype was assessed using semantic map analysis. MAIN OUTCOMES AND MEASURES: Association of HS with TH1/TH17 phenotype. RESULTS: The analysis was performed on 24 lesional HS biopsy samples from untreated patients with HS (16 [67%] female; median age, 36.5 years [range, 21-51 years]) with a mean (SD) Hurley stage of 2.29 (0.62) and 9 punch biopsy samples from healthy controls (6 [67%] female; median age, 43 years [range, 23-66 years]). The map shows a clustering of all TH1/TH17-associated cytokines (interleukin 17 [IL-17], interferon γ, IL-12, IL-23, IL-32, IL-1β, tumor necrosis factor) around overall lesional inflammation. Tumor necrosis factor, IL-12, and IL-17 are even directly connected via interferon γ. In contrast, IL-13, a TH2-associated cytokine, was inversely correlated with the presence of TH1/TH17-associated cytokines, further highlighting the importance of the TH1/TH17 cytokines in HS pathogenesis. CONCLUSIONS AND RELEVANCE: These findings suggest that HS may be a TH1/TH17-driven inflammatory skin disease. |
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ISSN: | 2168-6068 2168-6084 |
DOI: | 10.1001/jamadermatol.2018.0141 |