4.7 Article

Epithelialized tunnels are a source of inflammation in hidradenitis suppurativa

期刊

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
卷 147, 期 6, 页码 2213-2224

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MOSBY-ELSEVIER
DOI: 10.1016/j.jaci.2020.12.651

关键词

Hidradenitis suppurativa; IL-17; neutrophils; brodalumab

资金

  1. Medical Scientist Training Program grant from the National Institute of General Medical Sciences of the National Institutes of Health [T32GM007739]
  2. National Center for Advancing Translational Sciences, National Institutes of Health Clinical and Translational Science Award Program [UL1 TR001866]
  3. Shapiro-Silverberg Fund for the Advancement of Translational Research
  4. Hidradenitis Suppurativa Foundation Danby Grant

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The study found that tunnels in hidradenitis suppurativa (HS) play an immunologically active role in disease activity, showing inflammation characteristics and associated with increased infiltration of T cells, dendritic cells, and neutrophils. Treatment with medication reduced the size and draining of tunnels, indicating their involvement in disease inflammation.
Background: Hidradenitis suppurativa (HS), also known as acne inversa, is a chronic, painful, and burdensome inflammatory disease manifesting in nodules and abscesses, with progression to chronically draining tunnels in later-stage disease. Objective: We sought to determine whether HS tunnels are immunologically active participants in disease activity. Methods: Skin biopsy specimens were obtained by using ultrasound guidance in untreated patients with HS and those enrolled in an open-label study of brodalumab (ClinicalTrials.gov identifier NCT03960268) for patients with moderate-to-severe HS. Results: Immunohistochemistry of HS biopsy specimens demonstrated that the epithelialized HS tunnels recapitulate the psoriasiform epidermal hyperplasia morphology of the overlying epidermis, displaying molecular inflammation, including S100A7 (psoriasin) positivity, as well as features of epidermal skin, including loricrin, filaggrin, lipocalin-2, and Melan-A positive cells. Tunnels were associated with increased infiltration of T cells, dendritic cells, and neutrophils; formation of neutrophil extracellular traps, and increased expression of psoriasiform proinflammatory cytokines. Unsupervised hierarchical clustering demonstrated a separation of HS samples based on the presence or absence of tunnels. Tunnels isolated by microdissection had higher levels of epithelium derived inflammatory cytokines compared with the overlying epidermis and healthy controls. Clinically, the size and draining of the tunnels were decreased with treatment with the IL-17RA antagonist brodalumab. Conclusion: These data suggest that tunnels are a source of inflammation in HS. (J Allergy Clin Immunol 2021;147:2213-24.)

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