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类风湿关节炎肺部并发症患者的诱导性支气管相关淋巴组织(iBALT)

Inducible bronchus-associated lymphoid tissue (iBALT) in patients with pulmonary complications of rheumatoid arthritis.

作者信息

Rangel-Moreno Javier, Hartson Louise, Navarro Carmen, Gaxiola Miguel, Selman Moises, Randall Troy D

机构信息

Trudeau Institute, Saranac Lake, NY 12983, USA.

出版信息

J Clin Invest. 2006 Dec;116(12):3183-94. doi: 10.1172/JCI28756.

Abstract

Bronchus-associated lymphoid tissue (BALT) was originally described as a mucosal lymphoid organ in the lungs of some species. However, while the lungs of naive mice and humans typically lack BALT, pulmonary infection in mice leads to the development of inducible BALT (iBALT), which is located in peribronchial, perivascular, and interstitial areas throughout the lung. Here we investigated whether iBALT forms in patients with a variety of interstitial lung diseases. We show that while iBALT can be found in the lungs of patients suffering from multiple diseases, well-developed iBALT is most prevalent in patients with pulmonary complications of RA and Sjögren syndrome. In these patients, iBALT consisted of numerous B cell follicles containing germinal centers and follicular dendritic cells. A loosely defined T cell area surrounded the B cell follicles while lymphatics and high endothelial venules were found at the B cell/T cell interface. Increased expression of lymphoid-organizing chemokines, such as CXCL13 and CCL21, as well as molecules involved in the immunopathology of RA, such as B cell-activating factor of the TNF family (BAFF), ICOS ligand, and lymphotoxin, correlated with more well-developed iBALT. Finally, the presence of iBALT correlated with tissue damage in the lungs of RA patients, suggesting that iBALT participates in local RA pathogenesis.

摘要

支气管相关淋巴组织(BALT)最初被描述为某些物种肺部的一种黏膜淋巴器官。然而,尽管未接触过抗原的小鼠和人类的肺部通常缺乏BALT,但小鼠肺部感染会导致可诱导性BALT(iBALT)的形成,其位于肺内支气管周围、血管周围和间质区域。在此,我们研究了多种间质性肺疾病患者是否会形成iBALT。我们发现,虽然在患有多种疾病的患者肺部均可发现iBALT,但发育良好的iBALT在类风湿关节炎(RA)和干燥综合征肺部并发症患者中最为常见。在这些患者中,iBALT由众多含有生发中心和滤泡树突状细胞的B细胞滤泡组成。B细胞滤泡周围是界限不清的T细胞区,而在B细胞/T细胞界面发现了淋巴管和高内皮微静脉。淋巴组织趋化因子(如CXCL13和CCL21)以及参与RA免疫病理学的分子(如肿瘤坏死因子家族的B细胞活化因子(BAFF)、诱导共刺激分子配体和淋巴毒素)表达增加,与更发达的iBALT相关。最后,iBALT的存在与RA患者肺部的组织损伤相关,提示iBALT参与了局部RA的发病机制。

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本文引用的文献

1
Lymphoid organ development: from ontogeny to neogenesis.
Nat Immunol. 2006 Apr;7(4):344-53. doi: 10.1038/ni1330.
2
Citrullination is an inflammation-dependent process.
Ann Rheum Dis. 2006 Sep;65(9):1219-22. doi: 10.1136/ard.2005.049403. Epub 2006 Mar 15.
3
Lymphoid neogenesis in chronic inflammatory diseases.
Nat Rev Immunol. 2006 Mar;6(3):205-17. doi: 10.1038/nri1786.
5
Bronchus- and nasal-associated lymphoid tissues.
Immunol Rev. 2005 Aug;206:22-31. doi: 10.1111/j.0105-2896.2005.00299.x.
7
Frequency and potential cause of bronchus-associated lymphoid tissue in fetal lungs.
Pediatr Allergy Immunol. 2005 Jun;16(4):295-8. doi: 10.1111/j.1399-3038.2005.00269.x.
8
Clinical advances in the diagnosis and therapy of the interstitial lung diseases.
Am J Respir Crit Care Med. 2005 Aug 1;172(3):268-79. doi: 10.1164/rccm.200503-483OE. Epub 2005 May 5.
10
Lymphoid neogenesis in murine cardiac allografts undergoing chronic rejection.
Am J Transplant. 2005 Mar;5(3):510-6. doi: 10.1111/j.1600-6143.2004.00714.x.

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