Lichen planopilaris is characterized by immune privilege collapse of the hair follicle's epithelial stem cell niche

Matthew J. Harries, Katja Meyer, Iskander Chaudhry, Jennifer E Kloepper, Enrique Poblet, Christopher E.M. Griffiths, Ralf Paus

Research output: Contribution to journalArticle

86 Citations (Scopus)

Abstract

Lichen planopilaris (LPP) is a chronic inflammatory disease of unknown pathogenesis that leads to permanent hair loss. Whilst destruction of epithelial hair follicle stem cells (eHFSCs) that reside in an immunologically protected niche of the HF epithelium, the bulge, is a likely key event in LPP pathogenesis, this remains to be demonstrated. We have tested the hypotheses that bulge immune privilege (IP) collapse and inflammation-induced eHFSC death are key components in the pathogenesis of LPP. Biopsies of lesional and non-lesional scalp skin from adult LPP patients (n = 42) were analysed by quantitative (immuno)histomorphometry, real-time quantitative polymerase chain reaction (qRT-PCR), laser capture microdissection and microarray analysis, or skin organ culture. At both the protein and transcriptional level, lesional LPP HFs showed evidence for bulge IP collapse (ie increased expression of MHC class I and II, β2microglobulin; reduced TGFβ2 and CD200 expression). This was accompanied by a Th1-biased cytotoxic T cell response (ie increased CD8 + GranzymeB+ T cells and CD123+ plasmacytoid dendritic cells, with increased CXCR3 expression) and increased expression of interferon-inducible chemokines (CXCL9/10/11). Interestingly, lesional LPP eHFSCs showed both increased proliferation and apoptosis in situ. Microarray analysis revealed a loss of eHFSC signatures and increased expression of T cell activation/binding markers in active LPP, while bulge PPARγ transcription was unaltered compared to non-lesional LPP HFs. In organ culture of non-lesional LPP skin, interferon-γ (IFNγ) induced bulge IP collapse. LPP is an excellent model disease for studying and preventing immune destruction of human epithelial stem cells in situ. These novel findings raise the possibility that LPP represents an autoimmune disease in whose pathogenesis IFNγ-induced bulge IP collapse plays an important role. Therapeutically, bulge IP protection/restoration may help to better manage this highly treatment-resistant cicatricial alopecia.

Original languageEnglish (US)
Pages (from-to)236-247
Number of pages12
JournalJournal of Pathology
Volume231
Issue number2
DOIs
StatePublished - Oct 1 2013
Externally publishedYes

Fingerprint

Stem Cell Niche
Lichens
Hair Follicle
Epithelial Cells
Stem Cells
Interferons
Organ Culture Techniques
Alopecia
Microarray Analysis
T-Lymphocytes
Skin
Chemokine CXCL9
Laser Capture Microdissection
Peroxisome Proliferator-Activated Receptors
Scalp
Dendritic Cells
Autoimmune Diseases
Real-Time Polymerase Chain Reaction
Chronic Disease
Cell Death

Keywords

  • alopecia
  • frontal fibrosing alopecia
  • lichen planopilaris
  • pathogenesis

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

Cite this

Lichen planopilaris is characterized by immune privilege collapse of the hair follicle's epithelial stem cell niche. / Harries, Matthew J.; Meyer, Katja; Chaudhry, Iskander; E Kloepper, Jennifer; Poblet, Enrique; Griffiths, Christopher E.M.; Paus, Ralf.

In: Journal of Pathology, Vol. 231, No. 2, 01.10.2013, p. 236-247.

Research output: Contribution to journalArticle

Harries, MJ, Meyer, K, Chaudhry, I, E Kloepper, J, Poblet, E, Griffiths, CEM & Paus, R 2013, 'Lichen planopilaris is characterized by immune privilege collapse of the hair follicle's epithelial stem cell niche', Journal of Pathology, vol. 231, no. 2, pp. 236-247. https://doi.org/10.1002/path.4233
Harries, Matthew J. ; Meyer, Katja ; Chaudhry, Iskander ; E Kloepper, Jennifer ; Poblet, Enrique ; Griffiths, Christopher E.M. ; Paus, Ralf. / Lichen planopilaris is characterized by immune privilege collapse of the hair follicle's epithelial stem cell niche. In: Journal of Pathology. 2013 ; Vol. 231, No. 2. pp. 236-247.
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