Lymphocyte subsets in experimental rhinovirus infection in chronic obstructive pulmonary disease
Author(s)
Type
Journal Article
Abstract
Background
COPD is associated with increased numbers of T cells in the lungs, particularly CD8+ T cells. The mechanisms of increased T cells are unknown but may be related to repeated virus infections in COPD patients. We analysed lymphocyte subsets in blood and bronchoalveolar lavage in smokers and COPD subjects during experimental rhinovirus infections.
Methods
Lymphocytes were isolated from blood and bronchoalveolar lavage from COPD subjects and non-obstructed smokers prior to, and following experimental rhinovirus infection. Lymphocyte surface markers and intracellular cytokines were analysed using flow cytometry.
Results
Following rhinovirus infection CD4+ and CD8+ T cell numbers in the COPD subjects were significantly reduced in blood and CD3+ and CD8+ T cells increased in bronchoalveolar lavage compared to baseline. T cells did not increase in BAL in the control subjects. CD3+ T cells correlated with virus load.
Conclusions
Following rhinovirus infection T cells move from the circulation to the lung. Repeated virus infections may contribute to T cell accumulation in COPD patients.
COPD is associated with increased numbers of T cells in the lungs, particularly CD8+ T cells. The mechanisms of increased T cells are unknown but may be related to repeated virus infections in COPD patients. We analysed lymphocyte subsets in blood and bronchoalveolar lavage in smokers and COPD subjects during experimental rhinovirus infections.
Methods
Lymphocytes were isolated from blood and bronchoalveolar lavage from COPD subjects and non-obstructed smokers prior to, and following experimental rhinovirus infection. Lymphocyte surface markers and intracellular cytokines were analysed using flow cytometry.
Results
Following rhinovirus infection CD4+ and CD8+ T cell numbers in the COPD subjects were significantly reduced in blood and CD3+ and CD8+ T cells increased in bronchoalveolar lavage compared to baseline. T cells did not increase in BAL in the control subjects. CD3+ T cells correlated with virus load.
Conclusions
Following rhinovirus infection T cells move from the circulation to the lung. Repeated virus infections may contribute to T cell accumulation in COPD patients.
Date Issued
2014-01-01
Date Acceptance
2013-09-14
Citation
Respiratory Medicine, 2014, 108 (1), pp.78-85
ISSN
0954-6111
Publisher
Elsevier
Start Page
78
End Page
85
Journal / Book Title
Respiratory Medicine
Volume
108
Issue
1
Copyright Statement
© 2013 The Authors. Published by Elsevier Ltd.
Open access under CC BY license.
Open access under CC BY license.
License URL
Sponsor
Medical Research Council (MRC)
Medical Research Council (MRC)
Wellcome Trust
Identifier
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000331921600009&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
Grant Number
G1000758
G1000758
083567/Z/07/Z
Subjects
Science & Technology
Life Sciences & Biomedicine
Cardiac & Cardiovascular Systems
Respiratory System
Cardiovascular System & Cardiology
Chronic obstructive pulmonary disease
Acute exacerbations of COPD
Respiratory viruses
T lymphocytes
T-CELL APOPTOSIS
AIRWAY INFLAMMATION
PERIPHERAL AIRWAYS
SPUTUM
SMOKERS
EXACERBATIONS
ONSET
Publication Status
Published
Date Publish Online
2013-09-22