TY - JOUR
T1 - Association between airway hyperreactivity and bronchial macrophage dysfunction in individuals with mild asthma
AU - Alexis, Neil E.
AU - Soukup, Joleen
AU - Nierkens, Stefan
AU - Becker, Susanne
PY - 2001/2
Y1 - 2001/2
N2 - Little is known about the functional capabilities of bronchial macrophages (BMs) and their relationship to airway disease such as asthma. We hypothesize that BMs from asthmatics may be modulated in their function compared with similar cells from healthy individuals. BMs obtained by induced sputum from mild asthmatics (n = 20) and healthy individuals (n = 20) were analyzed using flow cytometry for CD16, CD64, CD11b, CD14, and human leukocyte antigen-DR expression, phagocytosis of IgG opsonized yeast, and oxidant production. Asthma status was assessed by lung function [percent predicted forced vital capacity and forced expiratory volume in 1 s (FEV1)], percent sputum eosinophils, and nonspecific airway responsiveness [provocative concentration that produces a 20% fall in FEV1 (PC20,FEV1)]. Asthmatics with >5% airway eosinophils (AEo+) had decreased BM CD64 expression and phagocytosis compared with asthmatics with <5% eosinophils (AEo-). Among asthmatics, a significant correlation was found between CD64 expression and BM phagocytosis (R = 0.7, P < 0.009). Phagocytosis was also correlated with PC20,FEV1 (R = 0.6, P < 0.007), lung function (%predicted FEV1, R = 0.7, P < 0.002) and percent eosinophils (R = -0.6, P < 0.01). In conclusion, BM from asthmatics are functionally modulated, possibly by Th2 cytokines involved in asthma pathology.
AB - Little is known about the functional capabilities of bronchial macrophages (BMs) and their relationship to airway disease such as asthma. We hypothesize that BMs from asthmatics may be modulated in their function compared with similar cells from healthy individuals. BMs obtained by induced sputum from mild asthmatics (n = 20) and healthy individuals (n = 20) were analyzed using flow cytometry for CD16, CD64, CD11b, CD14, and human leukocyte antigen-DR expression, phagocytosis of IgG opsonized yeast, and oxidant production. Asthma status was assessed by lung function [percent predicted forced vital capacity and forced expiratory volume in 1 s (FEV1)], percent sputum eosinophils, and nonspecific airway responsiveness [provocative concentration that produces a 20% fall in FEV1 (PC20,FEV1)]. Asthmatics with >5% airway eosinophils (AEo+) had decreased BM CD64 expression and phagocytosis compared with asthmatics with <5% eosinophils (AEo-). Among asthmatics, a significant correlation was found between CD64 expression and BM phagocytosis (R = 0.7, P < 0.009). Phagocytosis was also correlated with PC20,FEV1 (R = 0.6, P < 0.007), lung function (%predicted FEV1, R = 0.7, P < 0.002) and percent eosinophils (R = -0.6, P < 0.01). In conclusion, BM from asthmatics are functionally modulated, possibly by Th2 cytokines involved in asthma pathology.
KW - Asthma
KW - Bronchial macrophages
KW - CD11b
KW - CD64
KW - Flow cytometry analysis of surface receptors
KW - Induced sputum
KW - Phagocytosis
UR - http://www.scopus.com/inward/record.url?scp=0035018868&partnerID=8YFLogxK
U2 - 10.1152/ajplung.2001.280.2.l369
DO - 10.1152/ajplung.2001.280.2.l369
M3 - Article
C2 - 11159017
AN - SCOPUS:0035018868
SN - 1040-0605
VL - 280
SP - L369-L375
JO - American Journal of Physiology - Lung Cellular and Molecular Physiology
JF - American Journal of Physiology - Lung Cellular and Molecular Physiology
IS - 2 24-2
ER -