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PMID: 19845971 Published · epublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Expression of endothelia and lymphocyte adhesion molecules in bronchus-associated lymphoid tissue (BALT) in adult human lung.

Respiratory research ·Vol. 10 ·2009-10-22 ·Pages 97

Kawamata N, Xu B, Nishijima H, Aoyama K, Kusumoto M, Takeuchi T, Tei C, Michie SA, Matsuyama T

Abstract

Bronchus-associated lymphoid tissue (BALT) is the secondary lymphoid tissue in bronchial mucosa and is involved in the development of bronchopulmonary immune responses. Although migration of lymphocytes from blood vessels into secondary lymphoid tissues is critical for the development of appropriate adaptive immunity, the endothelia and lymphocyte adhesion molecules that recruit specific subsets of lymphocytes into human BALT are not known. The aim of this study was to determine which adhesion molecules are expressed on lymphocytes and high endothelial venules (HEVs) in human BALT. We immunostained frozen sections of BALT from lobectomy specimens from 17 patients with lung carcinoma with a panel of monoclonal antibodies to endothelia and lymphocyte adhesion molecules. Sections of BALT showed B cell follicles surrounded by T cells. Most BALT CD4+ T cells had a CD45RO+ memory phenotype. Almost all BALT B cells expressed alpha4 integrin and L-selectin. In contrast, 43% of BALT T cells expressed alpha4 integrin and 20% of BALT T cells expressed L-selectin. Almost all BALT lymphocytes expressed LFA-1. HEVs, which support the migration of lymphocytes from the bloodstream into secondary lymphoid tissues, were prominent in BALT. All HEVs expressed peripheral node addressin, most HEVs expressed vascular cell adhesion molecule-1, and no HEVs expressed mucosal addressin cell adhesion molecule-1. Human BALT expresses endothelia and lymphocyte adhesion molecules that may be important in recruiting naive and memory/effector lymphocytes to BALT during protective and pathologic bronchopulmonary immune responses.

MeSH Terms
Adult Antigens, Surface/analysis B-Lymphocytes/immunology Bronchi/immunology CD4-Positive T-Lymphocytes/immunology Cell Adhesion Molecules/analysis Humans Immunity, Innate Immunity, Mucosal Immunoglobulins/analysis Immunohistochemistry Immunologic Memory Immunophenotyping Integrin alpha4/analysis L-Selectin/analysis Lung Neoplasms/immunology,surgery Lymphatic Vessels/immunology Lymphocyte Function-Associated Antigen-1/analysis Lymphocytes/immunology Lymphoid Tissue/immunology Membrane Proteins/analysis Mucoproteins/analysis Pneumonectomy Vascular Cell Adhesion Molecule-1/analysis
Chemicals
Antigens, Surface Cell Adhesion Molecules Immunoglobulins L-selectin counter-receptors Lymphocyte Function-Associated Antigen-1 MADCAM1 protein, human Membrane Proteins Mucoproteins Vascular Cell Adhesion Molecule-1 L-Selectin Integrin alpha4
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Kawamata Nakaaki
Departments of Immunology, Graduate School of Medical and Dental Sciences, Kagoshima University, 8-35-1 Sakuragaoka, Kagoshima 890-8520, Japan. kawamata@po5.synapse.ne.jp
Xu Baohui
Nishijima Hiroo
Aoyama Kohji
Kusumoto Mayumi
Takeuchi Toru
Tei Chuwa
Michie Sara A
Matsuyama Takami
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Article Info
Journal
Respiratory research
Abbr.
Respir Res
ISSN
1465-993X
Published
2009-10-22
Epub
2009-00-22
Pages
97
Language
English
Region
England
NLM ID
101090633
PMCID
PMC2772857
Subset
IM
Grants
NIDDK NIH HHS · DK56339 · United States
NIDCR NIH HHS · R01 DE014385 · United States
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