Am. J. Respir. Crit. Care Med., Vol 150, No. 1, Jul 1994, 135-142.
Compartmentalized immune response reflects clinical severity of beryllium disease
LS Newman, C Bobka, B Schumacher, E Daniloff, B Zhen, MM Mroz and TE King Jr
Department of Medicine, National Jewish Center for Immunology and Respiratory Medicine, Denver, Colorado.
Although beryllium disease has been associated with a bronchoalveolar
lavage (BAL) lymphocytosis and T cell-mediated immune response, we do not
know if either the BAL cellular profile or the compartmentalized pulmonary
response to the antigen reflect the severity of the disease. We studied 110
subjects divided into three groups of subjects: beryllium disease patients
(n = 55), beryllium-sensitized patients without disease (n = 8), and
control subjects (n = 47). Evaluation included completion of a respiratory
symptom questionnaire, clinical examination, chest radiograph, spirometry,
body plethysmographic lung volumes, and diffusing capacity (DLCO). In the
patient groups, we performed maximal exercise testing with an indwelling
arterial line. In addition, we examined BAL and performed blood and BAL
beryllium lymphocyte transformation tests (BeLT) as measures of the
beryllium- specific T cell-mediated response in these two compartments. In
beryllium disease patients we correlated the BAL cellular constituents with
clinical parameters indicative of disease severity. Beryllium disease
patients exhibited elevated numbers of white cells and lymphocytes in BAL
compared with both other groups; however, this lymphocytic alveolitis was
significantly obscured in smokers. The BAL cellular constituents correlated
with BAL BeLT but not with the blood BeLT. BAL cellular constituents also
correlated with the radiographic profusion of small opacities, FEV1/FVC,
DLCO, maximal achievable work load, VO2max, and measures of gas exchange at
rest and at maximum exercise. We conclude that the lymphocyte-predominant
pulmonary inflammatory response in beryllium disease is related to the
magnitude of the localized response to antigen and that BAL cellularity,
differential cell count, and BeLT reflect beryllium disease clinical
severity.(ABSTRACT TRUNCATED AT 250 WORDS)
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Copyright © 1994 American Thoracic Society
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