4.7 Article

Myeloid Dendritic Cells Are Major Producers of IFN-β in Dermatomyositis and May Contribute to Hydroxychloroquine Refractoriness

Journal

JOURNAL OF INVESTIGATIVE DERMATOLOGY
Volume 141, Issue 8, Pages 1906-+

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jid.2020.12.032

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Funding

  1. National Institutes of Health [R21 AAR066286]
  2. Myositis Association
  3. Department of Veterans Affairs Veterans Health Administration
  4. Office of Research and Development, Biomedical Laboratory Research and Development
  5. Core A of the Penn Skin Biology and Diseases Resource-based Center [P30 AR069589-01]

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The pathogenesis of dermatomyositis involves a predominant IFN-1 response, with mDCs playing an important role in IFN-beta production in the skin. Patients with dermatomyositis have increased CD4+, CD11c+, and CD69+ cells in lesional skin, and both mDCs and plasmacytoid dendritic cells are major producers of IFN-beta in their blood. Additionally, mDCs are significantly increased in the skin of hydroxychloroquine nonresponders.
Dermatomyositis pathogenesis remains incompletely understood; however, recent work suggests a predominant IFN-1 response. We explored dermatomyositis pathogenesis by quantifying the inflammatory cells in the skin, comparing myeloid with plasmacytoid dendritic cell release of IFN-beta, and assessing myeloid dendritic cell (mDC) contribution to hydroxychloroquine refractoriness. Immunohistochemistry was performed to assess cell-type expression in lesional skin biopsies from 12 patients with moderate-to-severe cutaneous dermatomyositis. Immunofluorescence, laser-capture microdissection, and flow cytometry were used to assess mDC release of IFN-beta in lesional skin biopsies and blood of patients with dermatomyositis. Immunohistochemistry was utilized to determine whether myeloid or plasmacytoid dendritic cells were increased in hydroxychloroquine nonresponders. CD4+, CD11c+, and CD69+ cells were more populous in lesional skin of patients with dermatomyositis. mDCs colocalized with IFN-beta by immunofluorescence and laser-capture microdissection revealed increased IFN-beta mRNA expression by mDCs in lesional skin of patients with dermatomyositis. In blood, both mDCs and plasmacytoid dendritic cells were major producers of IFN-beta in patients with dermatomyositis, whereas plasmacytoid dendritic cells predominately released IFN-beta in healthy controls (P < 0.01). mDCs were significantly increased in the skin of hydroxychloroquine nonresponders compared with that in the skin of responders (P < 0.05). mDCs cells appear to play an important role in dermatomyositis pathogenesis and IFN-beta production.

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