CD163 and CD206 expression define distinct macrophage subsets involved in active ANCA-associated glomerulonephritis.
ANCA glomerulonephritis
Acute kidney injury
Kidney pathology
Macrophages
Vasculitis
Journal
Journal of autoimmunity
ISSN: 1095-9157
Titre abrégé: J Autoimmun
Pays: England
ID NLM: 8812164
Informations de publication
Date de publication:
12 2022
12 2022
Historique:
received:
26
06
2022
revised:
06
09
2022
accepted:
12
09
2022
pubmed:
3
10
2022
medline:
15
12
2022
entrez:
2
10
2022
Statut:
ppublish
Résumé
Macrophages are key players in the immunopathology of anti-neutrophil cytoplasmic antibody (ANCA) mediated-vasculitis (AAV) with glomerulonephritis (ANCA GN). Different macrophage phenotypes are expected to play distinct roles in ANCA GN. Macrophages expressing CD163 and CD206 are found in lesions associated with ANCA GN. Hence, we aimed to investigate the clinicopathological significance of CD206 and CD163 in ANCA GN in a multicenter retrospective cohort study. Patients with ANCA-associated vasculitis, with clinical data, serum and urine samples were included from three cohorts. Serum soluble CD206 (ssCD206) and urinary soluble CD163 (usCD163) levels were measured. Human kidney tissue samples (n = 53) were stained for CD206 and CD163 using immunohistochemistry and immunofluorescence, and findings were correlated with clinical and pathological data. In total, 210 patients were included (i.e., ANCA GN, n = 134; AAV without GN, n = 24; AAV in remission n = 52). Increased levels of both ssCD206 and usCD163 were seen in ANCA GN. High levels of ssCD206 declined after reaching remission, however, ssCD206 did not improve the accuracy of usCD163 to detect ANCA GN. Soluble markers correlated with histopathological findings. CD163 Our results confirm and extend the notion that CD206
Identifiants
pubmed: 36183584
pii: S0896-8411(22)00122-6
doi: 10.1016/j.jaut.2022.102914
pii:
doi:
Substances chimiques
CD163 antigen
0
Antibodies, Antineutrophil Cytoplasmic
0
Types de publication
Multicenter Study
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
102914Informations de copyright
Copyright © 2022 The Author(s). Published by Elsevier Ltd.. All rights reserved.