Literature DB >> 32473779

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

Yuki Sato1, Peter Boor2, Shingo Fukuma3, Barbara M Klinkhammer2, Hironori Haga4, Osamu Ogawa5, Jürgen Floege6, Motoko Yanagita7.   

Abstract

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

Entities:  

Keywords:  follicular dendritic cell; renal aging; renal inflammation; tertiary lymphoid tissues

Mesh:

Year:  2020        PMID: 32473779     DOI: 10.1016/j.kint.2020.02.023

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  20 in total

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6.  Exposure of female NZBWF1 mice to imiquimod-induced lupus nephritis at an early age via a unique mechanism that differed from spontaneous onset.

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7.  Tertiary lymphoid tissues in kidney diseases: a perspective for the pediatric nephrologist.

Authors:  Takahisa Yoshikawa; Yu Ho Lee; Yuki Sato; Motoko Yanagita
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9.  Advanced Tertiary Lymphoid Tissues in Protocol Biopsies are Associated with Progressive Graft Dysfunction in Kidney Transplant Recipients.

Authors:  Yu Ho Lee; Yuki Sato; Mitsuru Saito; Shingo Fukuma; Masaya Saito; Shigenori Yamamoto; Atsushi Komatsuda; Nobuhiro Fujiyama; Shigeru Satoh; Sang-Ho Lee; Peter Boor; Tomonori Habuchi; Jürgen Floege; Motoko Yanagita
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10.  Ectopic Germinal Centres with B and T Cells and Follicular Dendritic Cell Networks in Urethral Stricture Tissue: Possible Avenue for Immunological Treatments.

Authors:  Teresa Olsen Ekerhult; Ola Grimsholm; Jenny Magnusson; Christina Kåbjörn Gustafsson; Ralph Peeker
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