4.6 Article

Inflammasome activation and vitiligo/nonsegmental vitiligo progression

Journal

BRITISH JOURNAL OF DERMATOLOGY
Volume 170, Issue 4, Pages 816-823

Publisher

OXFORD UNIV PRESS
DOI: 10.1111/bjd.12691

Keywords

confocal microscopy; dermoscopy; melanoma; number needed to treat

Categories

Ask authors/readers for more resources

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)-1 beta 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-1 beta and kallikrein 7 on lesional and perilesional vitiligo skin. Results NLRP1 and IL-1 beta 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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available