Inflammasome activation and vitiligo/nonsegmental vitiligo progression

Br J Dermatol. 2014 Apr;170(4):816-23. doi: 10.1111/bjd.12691.

Abstract

Background: Polymorphisms of NLR (nucleotide-binding domain and leucine rich repeat containing) family, pyrin domain containing protein 1 (NLRP1) have been found in patients with vitiligo/nonsegmental vitiligo (NSV), and increased NLRP1 expression has been detected in the leading edge of lesional skin biopsies.

Objectives: To evaluate the presence and intensity of NLRP1 immunostaining in lesional and perilesional skin of patients with vitiligo/NSV and to search for possible correlations between NLRP1 and interleukin (IL)-1β expression, lymphocytic infiltrates and disease activity.

Methods: Of 14 consecutive vitiligo/NSV patients, eight had active disease [Vitiligo European Task Force (VETF) spreading score +1 to +5], one patient had stable disease and five patients had regressive disease (VETF spreading score -1 to -3). We performed immunostaining for NLRP1, B and T lymphocytes, IL-1β and kallikrein 7 on lesional and perilesional vitiligo skin.

Results: NLRP1 and IL-1β immunostaining in perilesional vitiligo/NSV skin was significantly associated with progressive disease (P = 0·009 and 0·04, respectively) and performed better than the simple detection of lymphocytic infiltrates.

Conclusions: Our findings suggest that markers of the NLRP1 inflammasome could be a useful test for assessing disease activity in addition to the detection of inflammatory infiltrates in the progressing margins of vitiligo/NSV lesions.

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism
  • Adolescent
  • Adult
  • Aged
  • Apoptosis Regulatory Proteins / metabolism
  • Biomarkers / metabolism
  • Case-Control Studies
  • Disease Progression
  • Female
  • Humans
  • Immunohistochemistry
  • Inflammasomes / metabolism*
  • Interleukin-1beta / metabolism
  • Kallikreins / metabolism
  • Lymphocytes / physiology
  • Male
  • Middle Aged
  • NLR Proteins
  • Vitiligo / diagnosis*

Substances

  • Adaptor Proteins, Signal Transducing
  • Apoptosis Regulatory Proteins
  • Biomarkers
  • Inflammasomes
  • Interleukin-1beta
  • NLR Proteins
  • NLRP1 protein, human
  • Kallikreins