Developmental stages of tertiary lymphoid tissue reflect local injury and inflammation in mouse and human kidneys.

follicular dendritic cell renal aging renal inflammation tertiary lymphoid tissues

Journal

Kidney international
ISSN: 1523-1755
Titre abrégé: Kidney Int
Pays: United States
ID NLM: 0323470

Informations de publication

Date de publication:
08 2020
Historique:
received: 01 10 2018
revised: 18 02 2020
accepted: 20 02 2020
pubmed: 1 6 2020
medline: 22 6 2021
entrez: 1 6 2020
Statut: ppublish

Résumé

Tertiary lymphoid tissues (TLTs) are inducible ectopic lymphoid tissues in chronic inflammatory states and function as sites of priming local immune responses. We previously demonstrated that aged but not young mice exhibited multiple TLTs after acute kidney injury and that TLTs were also detected in human aged and diseased kidneys. However, the forms of progression and the implication for kidney injury remain unclear. To clarify this we analyzed surgically resected kidneys from aged patients with or without chronic kidney disease as well as kidneys resected for pyelonephritis, and classified TLTs into three distinct developmental stages based on the presence of follicular dendritic cells and germinal centers. In injury-induced murine TLT models, the stages advanced with the extent of kidney injury, and decreased with dexamethasone accompanied with improvement of renal function, fibrosis and inflammation. Kidneys from aged patients with chronic kidney disease consistently exhibited more frequent and advanced stages of TLTs than those without chronic kidney disease. Kidneys of patients with pyelonephritis exhibited more frequent TLTs with more advanced stages than aged kidneys. Additionally, TLTs in both cohorts shared similar locations and components, suggesting that TLT formation may not be a disease-specific phenomenon but rather a common pathological process. Thus, our findings provide the insights into biological features of TLT in the kidney and implicate TLT stage as a potential marker reflecting local injury and inflammation.

Identifiants

pubmed: 32473779
pii: S0085-2538(20)30265-9
doi: 10.1016/j.kint.2020.02.023
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

448-463

Informations de copyright

Copyright © 2020 International Society of Nephrology. Published by Elsevier Inc. All rights reserved.

Auteurs

Yuki Sato (Y)

Department of Nephrology, Graduate School of Medicine, Kyoto University, Kyoto, Japan; Medical Innovation Center TMK Project, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Peter Boor (P)

Institute of Pathology, Rhenish-Westphalian Technical University of Aachen, Aachen, Germany; Department of Nephrology, Rhenish-Westphalian Technical University of Aachen, Aachen, Germany.

Shingo Fukuma (S)

Human Health Sciences, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Barbara M Klinkhammer (BM)

Institute of Pathology, Rhenish-Westphalian Technical University of Aachen, Aachen, Germany; Department of Nephrology, Rhenish-Westphalian Technical University of Aachen, Aachen, Germany.

Hironori Haga (H)

Department of Diagnostic Pathology, Kyoto University Hospital, Kyoto, Japan.

Osamu Ogawa (O)

Department of Urology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Jürgen Floege (J)

Department of Nephrology, Rhenish-Westphalian Technical University of Aachen, Aachen, Germany.

Motoko Yanagita (M)

Department of Nephrology, Graduate School of Medicine, Kyoto University, Kyoto, Japan; Institute for the Advanced Study of Human Biology (ASHBi), Kyoto University, Kyoto, Japan. Electronic address: motoy@kuhp.kyoto-u.ac.jp.

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Classifications MeSH