» Articles » PMID: 10413722

Variation of Bronchoalveolar Lymphocyte Phenotypes with Age in the Physiologically Normal Human Lung

Overview
Journal Thorax
Date 1999 Jul 22
PMID 10413722
Citations 31
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Changes in T lymphocyte subsets have been observed in various forms of pulmonary disease. However, bronchoalveolar lymphocyte subsets have not been well characterised for healthy individuals differing in age. A study was undertaken to investigate the bronchoalveolar lavage (BAL) and peripheral blood lymphocyte subsets in clinically normal volunteers of two different age groups (19-36 and 64-83 years).

Methods: Bronchoalveolar lavage was performed on all individuals in both age groups and peripheral venous blood was drawn just prior to BAL. Bronchoalveolar cell profiles were characterised by morphological criteria, and cell surface antigen expression of lymphocytes was determined by flow cytometry.

Results: A significant increase in total BAL lymphocytes was observed for the oldest group compared with the youngest age group. Mean lymphocyte subset (CD4+/CD8+) ratios were significantly increased in BAL fluid from the older group compared with the younger group (mean (SE) 7.6 (1.5) vs 1.9 (0.2); p<0.0001). The increase in the BAL CD4+/CD8+ T cell ratio was mostly due to an increase in relative numbers of CD4+ lymphocytes, and the BAL CD4/CD8 ratio was disproportionately increased compared with peripheral blood in the older group. Increased expression of HLA-DR and CD69 on CD4+ T lymphocytes was observed in the oldest age group. Relative numbers of natural killer (NK) cells did not vary with age, and gammadelta T cells and CD5+ B cells were present in very low numbers in both age groups.

Conclusions: CD4+ T cells accumulate in air spaces of the lower respiratory tract with age in healthy adults and express increased amounts of HLA-DR and CD69 on their surfaces, suggesting a relative degree of CD4+ T lymphocyte activation for healthy older individuals who have normal lung function.

Citing Articles

Advancements in adoptive CAR immune cell immunotherapy synergistically combined with multimodal approaches for tumor treatment.

Chang Y, Chang M, Bao X, Dong C Bioact Mater. 2024; 42:379-403.

PMID: 39308543 PMC: 11415837. DOI: 10.1016/j.bioactmat.2024.08.046.


Bronchoalveolar lavage fluid analysis in patients with checkpoint inhibitor pneumonitis.

Chen R, Shi Y, Fang N, Shao C, Huang H, Pan R Cancer Immunol Immunother. 2024; 73(11):235.

PMID: 39271538 PMC: 11399518. DOI: 10.1007/s00262-024-03834-y.


A framework for exclusion of alternative diagnoses in sarcoidosis.

Harper L, Farver C, Yadav R, Culver D J Autoimmun. 2024; 149:103288.

PMID: 39084998 PMC: 11791745. DOI: 10.1016/j.jaut.2024.103288.


Liver-directed gene therapy attenuates progression of spontaneous and tobacco smoke-induced emphysema in α1-antitrypsin null mice.

Zieger M, Borel F, Greer C, Gernoux G, Blackwood M, Flotte T Mol Ther Methods Clin Dev. 2022; 25:425-438.

PMID: 35592360 PMC: 9097330. DOI: 10.1016/j.omtm.2022.04.003.


Short palate, lung, and nasal epithelial clone 1 (SPLUNC1) level determines steroid-resistant airway inflammation in aging.

Jaiswal A, Yadav J, Makhija S, Sandey M, Suryawanshi A, Mitra A Am J Physiol Lung Cell Mol Physiol. 2021; 322(1):L102-L115.

PMID: 34851736 PMC: 8759962. DOI: 10.1152/ajplung.00315.2021.


References
1.
Hallgren H, BUCKLEY 3rd C, Gilbertsen V, Yunis E . Lymphocyte phytohemagglutinin responsiveness, immunoglobulins and autoantibodies in aging humans. J Immunol. 1973; 111(4):1101-7. View

2.
Nagelkerken L, Dobber R, Drager A . Age-related changes in lymphokine production related to a decreased number of CD45RBhi CD4+ T cells. Eur J Immunol. 1991; 21(2):273-81. DOI: 10.1002/eji.1830210206. View

3.
Kraal G, Weissman I, Butcher E . Genetic control of T-cell subset representation in inbred mice. Immunogenetics. 1983; 18(6):585-92. DOI: 10.1007/BF00345966. View

4.
Crawford J, Eye M, Cohen H . Evaluation of monoclonal gammopathies in the "well" elderly. Am J Med. 1987; 82(1):39-45. DOI: 10.1016/0002-9343(87)90375-5. View

5.
Cosulich M, Rubartelli A, Risso A, Cozzolino F, Bargellesi A . Functional characterization of an antigen involved in an early step of T-cell activation. Proc Natl Acad Sci U S A. 1987; 84(12):4205-9. PMC: 305053. DOI: 10.1073/pnas.84.12.4205. View