Elevated cutaneous expression of stem cell factor in chronic spontaneous urticaria: a prospective cohort study.


Journal

Clinical and experimental dermatology
ISSN: 1365-2230
Titre abrégé: Clin Exp Dermatol
Pays: England
ID NLM: 7606847

Informations de publication

Date de publication:
04 Jul 2024
Historique:
received: 19 01 2024
revised: 20 06 2024
accepted: 02 07 2024
medline: 4 7 2024
pubmed: 4 7 2024
entrez: 4 7 2024
Statut: aheadofprint

Résumé

Tissue expression of endothelial cell (EC) markers of microcirculatory changes in CSU is poorly investigated. to explore the expression of specific EC markers (stem cell factor (SCF), vascular endothelial growth factor (VEGF) and membrane attack complex (MAC)) in CSU-L and CSU-NL skin through immunohistochemistry (IHC) and in serum. Lesional (L) and non-lesional (NL) skin biopsies from CSU patients and HCs were studied for the IHC expression of SCF, VEGF and MAC in CSU patients (n = 23) and healthy controls (HCs, n = 9). In this population, we also investigated blood levels of VEGF and SCF. Patients were also assessed for clinical characteristics, disease activity, and markers of autoimmune CSU (aiCSU). Epidermal SCF reactivity was significantly higher in CSU-L skin compared to HC skin (p=0.026). In the dermis, SCF immunoreactivity was seen particularly on endothelial, perivascular and epithelial cells. In CSU-L skin, mean perivascular SCF stainings were significantly more intense compared to HCs (p<0.001). Furthermore, CSU-NL skin also showed significantly higher SCF stainings on dermal perivascular cells compared to HCs (p<0.001). CSU patients had the highest SCF immunoreactivity scores in the epidermis and/or on dermal ECs. These patients did not have significantly higher SCF serum levels. This is the first study to show elevated cutaneous expression of SCF in chronic spontaneous urticaria. These findings underline the potential therapeutic possibilities of anti-KIT antibodies in CSU treatment.

Sections du résumé

BACKGROUND BACKGROUND
Tissue expression of endothelial cell (EC) markers of microcirculatory changes in CSU is poorly investigated.
OBJECTIVE OBJECTIVE
to explore the expression of specific EC markers (stem cell factor (SCF), vascular endothelial growth factor (VEGF) and membrane attack complex (MAC)) in CSU-L and CSU-NL skin through immunohistochemistry (IHC) and in serum.
METHODS METHODS
Lesional (L) and non-lesional (NL) skin biopsies from CSU patients and HCs were studied for the IHC expression of SCF, VEGF and MAC in CSU patients (n = 23) and healthy controls (HCs, n = 9). In this population, we also investigated blood levels of VEGF and SCF. Patients were also assessed for clinical characteristics, disease activity, and markers of autoimmune CSU (aiCSU).
RESULTS RESULTS
Epidermal SCF reactivity was significantly higher in CSU-L skin compared to HC skin (p=0.026). In the dermis, SCF immunoreactivity was seen particularly on endothelial, perivascular and epithelial cells. In CSU-L skin, mean perivascular SCF stainings were significantly more intense compared to HCs (p<0.001). Furthermore, CSU-NL skin also showed significantly higher SCF stainings on dermal perivascular cells compared to HCs (p<0.001). CSU patients had the highest SCF immunoreactivity scores in the epidermis and/or on dermal ECs. These patients did not have significantly higher SCF serum levels.
CONCLUSION CONCLUSIONS
This is the first study to show elevated cutaneous expression of SCF in chronic spontaneous urticaria. These findings underline the potential therapeutic possibilities of anti-KIT antibodies in CSU treatment.

Identifiants

pubmed: 38963799
pii: 7706090
doi: 10.1093/ced/llae252
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of British Association of Dermatologists. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.

Auteurs

Yora Mostmans (Y)

Department of Immunology-Allergology, CHU Brugmann, Université Libre de Bruxelles (ULB), Laken, Belgium.
Department of Dermatology, CHU Brugmann, ULB, Laken, Belgium.

Katleen De Smedt (K)

Vrije Universiteit Brussel (VUB), Universitair Ziekenhuis Brussel (UZ Brussel), Department of Pathology, Brussels, Belgium.

Francesco Feoli (F)

Department of Dermatopathology, CHU Saint-Pierre, Brussel.

Wim Waelput (W)

Vrije Universiteit Brussel (VUB), Universitair Ziekenhuis Brussel (UZ Brussel), Department of Pathology, Brussels, Belgium.

Viviane De Maertelaer (V)

IRIBHM, statistical Unit, Fac. Medicine, ULB, Brussels, Belgium.

Cathérine Olemans (C)

Department of Dermatopathology, CHU Saint-Pierre, Brussel.

Isabelle Meiers (I)

Department of Dermatopathology, CHU Saint-Pierre, Brussel.

Thierry Cielen (T)

Department of Anatomopathology, Institut Jules Bordet, Brussels, Belgium.

Francis Corazza (F)

Department of Immunology, Laboratoire Hospitalier Universitaire de Bruxelles - Universitair Laboratorium Brussels (LHUB-ULB), Brussels, Belgium.

Olivier Michel (O)

Department of Immunology-Allergology, CHU Brugmann, Université Libre de Bruxelles (ULB), Laken, Belgium.
Hôpital Delta (CHIREC) and Université Libre de Bruxelles (ULB), Brussels, Belgium.

Bertrand Richert (B)

Department of Dermatology, CHU Brugmann, ULB, Laken, Belgium.

Classifications MeSH