Am. J. Respir. Crit. Care Med., Vol 155, No. 3, Mar 1997, 858-863.
Phenotypic analysis of alveolar macrophages and monocytes in allergic airway inflammation. I. Evidence for activation of alveolar macrophages, but not peripheral blood monocytes, in subjects with allergic rhinitis and asthma
MY Viksman, MC Liu, CA Bickel, RP Schleimer and BS Bochner
Department of Medicine, Johns Hopkins University School of Medicine, Johns Hopkins Asthma and Allergy Center, Baltimore, Maryland 21224- 6801, USA.
Macrophages and monocytes play important proinflammatory roles in allergic
inflammation. We hypothesized that these cells would express an activated
phenotype in allergic disease of the airways. We therefore compared the
expression of 17 activation markers on the surface of alveolar macrophages
(AM) and peripheral blood monocytes (PBM) in 13 subjects with asymptomatic
allergic asthma (AA), nine subjects with asymptomatic allergic rhinitis
(AR), and 11 nonallergic (N). AM were obtained by BAL, and PBM were
simultaneously obtained by phlebotomy; both were analyzed for expression of
surface markers using a new two- color flow cytometry method that
essentially eliminates background autofluorescence. The proportions of AM
in BAL fluid from AA, AR, and N subjects were 84 +/- 2, 85 +/- 4, and 91
+/- 1%, respectively; viability always exceeded 92%. Expression of eight
markers (CD16, CD18, CD32, CD44, CD71, HLA Class I, HLA DR, and HLA DQ) was
significantly (p < 0.05) higher on AM of AA than on N; expression of six
markers (CD11a, CD16, CD18, CD71, HLA Class I, and HLA DR) was higher on AM
of AR than on N, with differences in CD44 levels approaching statistical
significance (p = 0.07). Expression of one marker, CD44, was significantly
higher on AM of AA than on those of AR, with differences in HLA Class I
levels approaching statistical significance (p = 0.07). In contrast, no
significant differences were found among the three groups in the expression
in eight other markers (CD11b, CD14, CD23, CD29, CD33, CD35, CD63, and
CD64). Finally, similar analysis of PBM from these same subjects failed to
find any difference between the three groups in any of the 17 activation
markers studied. These data suggest that AM are activated in allergic
respiratory diseases, and that levels of HLA Class I and CD44 on AM are
altered during allergic inflammation in the upper and lower airways.
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Copyright © 1997 American Thoracic Society
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