Distinct macrophage phenotypes skewed by local granulocyte macrophage colony-stimulating factor (GM-CSF) and macrophage colony-stimulating factor (M-CSF) are associated with tissue destruction and intimal hyperplasia in giant cell arteritis.

giant cell arteritis granulocyte macrophage colony‐stimulating factor macrophage colony‐stimulating factor macrophages vasculitis

Journal

Clinical & translational immunology
ISSN: 2050-0068
Titre abrégé: Clin Transl Immunology
Pays: Australia
ID NLM: 101638268

Informations de publication

Date de publication:
2020
Historique:
received: 24 03 2020
revised: 10 07 2020
accepted: 11 07 2020
entrez: 5 9 2020
pubmed: 5 9 2020
medline: 5 9 2020
Statut: epublish

Résumé

To determine the presence and spatial distribution of different macrophage phenotypes, governed by granulocyte macrophage colony-stimulating factor (GM-CSF) and macrophage colony-stimulating factor (M-CSF) skewing signals, in giant cell arteritis (GCA) lesions. Temporal artery biopsies (TABs, A distinct spatial distribution pattern of macrophage phenotypes in TABs was identified. CD206 Our data document a distinct spatial distribution pattern of CD206

Identifiants

pubmed: 32884747
doi: 10.1002/cti2.1164
pii: CTI21164
pmc: PMC7453134
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e1164

Informations de copyright

© 2020 The Authors. Clinical & Translational Immunology published by John Wiley & Sons Australia, Ltd on behalf of Australian and New Zealand Society for Immunology Inc.

Déclaration de conflit d'intérêts

The authors declare no conflict of interest. AMHB was a consultant for Grünenthal Gmbh until 2017. EB and KvdG as employees of the UMCG received speaker/consulting fees from Roche which were paid to the UMCG. PH, WHA and EB have received funding from the European Union's Horizon 2020 research and innovation programme under grant agreement 668036.

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Auteurs

William F Jiemy (WF)

Department of Pathology and Medical Biology University of Groningen University Medical Center Groningen Groningen The Netherlands.
Faculty of Applied Science UCSI University UCSI Heights Cheras, Kuala Lumpur Malaysia.

Yannick van Sleen (Y)

Department of Rheumatology and Clinical Immunology University of Groningen University Medical Center Groningen Groningen The Netherlands.

Kornelis Sm van der Geest (KS)

Department of Rheumatology and Clinical Immunology University of Groningen University Medical Center Groningen Groningen The Netherlands.

Hilde A Ten Berge (HA)

Department of Pathology and Medical Biology University of Groningen University Medical Center Groningen Groningen The Netherlands.

Wayel H Abdulahad (WH)

Department of Pathology and Medical Biology University of Groningen University Medical Center Groningen Groningen The Netherlands.
Department of Rheumatology and Clinical Immunology University of Groningen University Medical Center Groningen Groningen The Netherlands.

Maria Sandovici (M)

Department of Rheumatology and Clinical Immunology University of Groningen University Medical Center Groningen Groningen The Netherlands.

Annemieke Mh Boots (AM)

Department of Rheumatology and Clinical Immunology University of Groningen University Medical Center Groningen Groningen The Netherlands.

Peter Heeringa (P)

Department of Pathology and Medical Biology University of Groningen University Medical Center Groningen Groningen The Netherlands.

Elisabeth Brouwer (E)

Department of Rheumatology and Clinical Immunology University of Groningen University Medical Center Groningen Groningen The Netherlands.

Classifications MeSH