L. Beijer et al., MONOCYTE RESPONSIVENESS AND A T-CELL SUBTYPE PREDICT THE EFFECTS INDUCED BY COTTON DUST EXPOSURE, American journal of respiratory and critical care medicine, 152(4), 1995, pp. 1215-1220
Citations number
36
Categorie Soggetti
Emergency Medicine & Critical Care","Respiratory System
The aim of the study was to evaluate whether peripheral cellular param
eters could predict susceptibility to decreased lung function and asso
ciated symptoms, in response to a single exposure to cotton dust. Prev
iously nonexposed subjects (n = 42) inhaled an aerosol of cotton dust
in a model cardroom during a period of 5 h. The subjects were examined
before the exposure for FEV(1), procoagulant activity (PCA) in blood
mononuclear cells (BMNC), and serum IgE antibodies against a pool of i
nhalant antigens. Blood lymphocytes were typed into the helper/inducer
(CD4+) and cytotoxic/suppressor (CD8+)T cells in combination with sur
face markers subdividing these populations. A questionnaire was used t
o identify atopic and nonatopic subjects. Immediately after exposure,
the subjects were tested for FEV(1) and PCA, and symptoms were recorde
d with a questionnaire. The dust exposure induced a decrease in FEV(1)
that was larger for the atopic group, but did not change the PCA in B
MNC. The decrease in FEV(1) was positively related to the preexposure
PCA in both atopics and nonatopics. Symptoms from the airways after th
e exposure were reported to the same extent in the atopic and nonatopi
c group, and the subject group reporting chest tightness had a larger
preexposure PCA. The atopic group had a larger proportion of blood CD8
+ T lymphocytes negative for the monoclonal antibody anti-S6f1 (CD8+S6
F1-), and in this group the decrease in FEV(1) was significantly relat
ed to the proportion of this cell type. Also, in the atopic group, the
proportion of CD8+S6F1- cells correlated positively with the preexpos
ure PCA, and a negative correlation was found for this cell and serum
levels of IgE. The findings suggest that functional changes induced by
an inflammatory response in the airways are related to cell reactivit
y and function in both atopic and nonatopic subjects.