Go to The Journal of Clinical Investigation
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
  • Physician-Scientist Development
  • Current issue
  • Past issues
  • By specialty
    • COVID-19
    • Cardiology
    • Immunology
    • Metabolism
    • Nephrology
    • Oncology
    • Pulmonology
    • All ...
  • Videos
  • Collections
    • In-Press Preview
    • Resource and Technical Advances
    • Clinical Research and Public Health
    • Research Letters
    • Editorials
    • Perspectives
    • Physician-Scientist Development
    • Reviews
    • Top read articles

  • Current issue
  • Past issues
  • Specialties
  • In-Press Preview
  • Resource and Technical Advances
  • Clinical Research and Public Health
  • Research Letters
  • Editorials
  • Perspectives
  • Physician-Scientist Development
  • Reviews
  • Top read articles
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
Contribution of plasma cells and B cells to hidradenitis suppurativa pathogenesis
Johann E. Gudjonsson, … , Robert L. Modlin, Errol P. Prens
Johann E. Gudjonsson, … , Robert L. Modlin, Errol P. Prens
Published August 27, 2020
Citation Information: JCI Insight. 2020;5(19):e139930. https://doi.org/10.1172/jci.insight.139930.
View: Text | PDF
Research Article Dermatology Immunology

Contribution of plasma cells and B cells to hidradenitis suppurativa pathogenesis

  • Text
  • PDF
Abstract

Hidradenitis suppurativa (HS) is a debilitating chronic inflammatory skin disease characterized by chronic abscess formation and development of multiple draining sinus tracts in the groin, axillae, and perineum. Using proteomic and transcriptomic approaches, we characterized the inflammatory responses in HS in depth, revealing immune responses centered on IFN-γ, IL-36, and TNF, with lesser contribution from IL-17A. We further identified B cells and plasma cells, with associated increases in immunoglobulin production and complement activation, as pivotal players in HS pathogenesis, with Bruton’s tyrosine kinase (BTK) and spleen tyrosine kinase (SYK) pathway activation as a central signal transduction network in HS. These data provide preclinical evidence to accelerate the path toward clinical trials targeting BTK and SYK signaling in moderate-to-severe HS.

Authors

Johann E. Gudjonsson, Lam C. Tsoi, Feiyang Ma, Allison C. Billi, K.R. van Straalen, A.R.J.V. Vossen, H.H. van der Zee, Paul W. Harms, Rachael Wasikowski, Christine M. Yee, Syed M. Rizvi, Xianying Xing, Enze Xing, Olesya Plazyo, Chang Zeng, Matthew T. Patrick, Margaret M. Lowe, Richard E. Burney, Jeffrey H. Kozlow, Jill R. Cherry-Bukowiec, Yanyun Jiang, Joseph Kirma, Stephan Weidinger, Kelly C. Cushing, Michael D. Rosenblum, Celine Berthier, Amanda S. MacLeod, John J. Voorhees, Fei Wen, J. Michelle Kahlenberg, Emanual Maverakis, Robert L. Modlin, Errol P. Prens

×

Figure 6

B and plasma cells are the dominant infiltrating leukocytes in HS.

Options: View larger image (or click on image) Download as PowerPoint
B and plasma cells are the dominant infiltrating leukocytes in HS.
Analy...
Analysis of the CyTOF data by t-distributed stochastic neighbor embedding (t-SNE) dimensionality reduction demonstrated clear separation between HS and normal skin (A) (scale bar: 100 μm), with the staining forming 14 distinct Phenograph clusters, of which only 2 were found in normal skin (B and C). Heatmap showing marker expression of each cluster (D). Quantification of the different subsets based on surface markers (E) (n = 3, Student’s t test, **P < 0.01; *P < 0.05; NS, nonsignificant).

Copyright © 2025 American Society for Clinical Investigation
ISSN 2379-3708

Sign up for email alerts