TY - JOUR
T1 - Immunomodulator galectin-9 is increased in blood and skin of patients with bullous pemphigoid
AU - Pruessmann, Jasper
AU - Pruessmann, Wiebke
AU - Holtsche, Maike M.
AU - Linnemann, Beke
AU - Hammers, Christoph M.
AU - Van Beek, Nina
AU - Zillikens, Detlef
AU - Schmidt, Enno
AU - Sadik, Christian D.
N1 - Publisher Copyright:
© 2021, Medical Journals/Acta D-V. All rights reserved.
PY - 2021
Y1 - 2021
N2 - Massive recruitment of eosinophils into the dermis is a hallmark of bullous pemphigoid pathogenesis. Identifying the chemoattractant(s) guiding eosinophils into the skin in bullous pemphigoid is a prerequisite to therapeutic targeting of eosinophil recruitment. Galectin -9 is a potent chemoattractant for eosinophils, but its potential role in bullous pemphigoid is unknown. The aim of this study was to determine the expression levels of galectin-9 in serum and skin of patients with bullous pemphigoid. Galectin-9 levels were significantly elevated in serum of patients with bullous pemphigoid compared with age- and sex-matched controls, but did not correlate with disease activity assessed with the Bullous Pemphigoid Disease Area Index. Galectin-9 expression was also increased in lesional skin of patients with bullous pemphigoid, and was expressed predominantly in eosinophils, neutrophils and keratinocytes. In conclusion, these results support the notion that galectin-9 may play a role in the pathogenesis of bullous pemphigoid.
AB - Massive recruitment of eosinophils into the dermis is a hallmark of bullous pemphigoid pathogenesis. Identifying the chemoattractant(s) guiding eosinophils into the skin in bullous pemphigoid is a prerequisite to therapeutic targeting of eosinophil recruitment. Galectin -9 is a potent chemoattractant for eosinophils, but its potential role in bullous pemphigoid is unknown. The aim of this study was to determine the expression levels of galectin-9 in serum and skin of patients with bullous pemphigoid. Galectin-9 levels were significantly elevated in serum of patients with bullous pemphigoid compared with age- and sex-matched controls, but did not correlate with disease activity assessed with the Bullous Pemphigoid Disease Area Index. Galectin-9 expression was also increased in lesional skin of patients with bullous pemphigoid, and was expressed predominantly in eosinophils, neutrophils and keratinocytes. In conclusion, these results support the notion that galectin-9 may play a role in the pathogenesis of bullous pemphigoid.
UR - http://www.scopus.com/inward/record.url?scp=85103086388&partnerID=8YFLogxK
U2 - 10.2340/00015555-3771
DO - 10.2340/00015555-3771
M3 - Journal articles
C2 - 33606034
AN - SCOPUS:85103086388
SN - 0001-5555
VL - 101
SP - adv00419
JO - Acta Dermato-Venereologica
JF - Acta Dermato-Venereologica
IS - 3
M1 - adv00419
ER -