Am. J. Respir. Crit. Care Med., Vol 153, No. 3, Mar 1996, 1072-1079.
Immune dysregulation in the aging human lung
KC Meyer, W Ershler, NS Rosenthal, XG Lu and K Peterson
Department of Medicine, University of Wisconsin Medical School, Madison 53792-3240, USA.
Aging has been associated with diminished lung function and increased
susceptibility to lung infection. To determine whether changes suggestive
of immune dysregulation and inflammation appear in the lungs of clinically
normal individuals as a function of advancing age, we performed
bronchoalveolar lavage (BAL) on discontinuous age groups (20- 36, 45-55,
and 65-78 yr old) of clinically normal volunteer subjects. We measured
immunoglobulin (IgG, IgA, IgM), albumin, interleukin-6 (IL- 6), and
interleukin-10 concentrations in BAL fluid. Bronchoalveolar cell profiles,
cell surface antigen expression, and superoxide anion production were also
measured. A significant increase in total cell concentration, neutrophils,
and BAL immunoglobulin content was observed in the oldest age group
compared with the youngest age group. Mean lymphocyte subset (CD4+/CD8+)
ratios were significantly increased in blood (2.6 +/- 0.4 versus 1.6 +/-
0.1; p<0.03) and to a greater degree in BAL (4.8 +/- 1.0 versus 1.9 +/-
0.2; p<0.01) for the oldest versus youngest age groups. Similarly,
BAL-derived cells displayed significantly increased phorbol myristate
acetate-stimulated release of superoxide anion (8.8 +/- 1.3 versus 4.5 +/-
0.7 nmol/5 x 10 5 cells/h; p<0.01) for the oldest versus youngest
subject group, and mean BAL IL-6 concentrations were significantly elevated
in the oldest age group (0.86 +/- 0.13 ng/ml) compared with the youngest
age group (0.53 +/- 0.03 ng/ml; p<0.01). Our observations suggest that
altered inflammatory cell profiles and low-grade inflammation exist in the
lower respiratory tracts of many asymptomatic, clinically normal volunteers
of advanced age.
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Copyright © 1996 American Thoracic Society
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