TY - JOUR
T1 - Evidence for systemic rather than pulmonary effects of interleukin-5 administration in asthma
AU - Van Rensen, E. L.J.
AU - Stirling, R. G.
AU - Scheerens, J.
AU - Staples, K.
AU - Sterk, P. J.
AU - Barnes, P. J.
AU - Chung, K. F.
PY - 2001/12/10
Y1 - 2001/12/10
N2 - Background - Interleukin 5 (IL-5) has an important role in mobilisation of eosinophils from the bone marrow and in their subsequent terminal differentiation. A study was undertaken to determine whether inhaled and intravenous IL-5 could induce pulmonary eosinophilia and bronchial hyperresponsiveness (BHR) independently of these effects. Methods - Nine mild asthmatics received inhaled (15 μg) or intravenous (2 μg) IL-5 or placebo in random order in a double blind, crossover study. Blood samples were taken before and at 0.5, 1, 2, 3, 4, 5, 24, and 72 hours following IL-5 or placebo, and bronchial responsiveness (PC20 methacholine) and eosinophil counts in induced sputum were determined. Results - Serum IL-5 levels were markedly increased 30 minutes after intravenous IL-5 (p=0.002), and sputum IL-5 levels increased 4 and 24 hours after inhaled IL-5 (p<0.05). Serum eotaxin was raised 24 hours after intravenous IL-5 but not after inhaled IL-5 or placebo. Blood eosinophils were markedly reduced 0.5-2 hours after intravenous IL-5 (p<0.05), followed by an increase at 3, 4, 5, and 72 hours (p<0.05). Sputum eosinophils rose significantly in all three groups at 24 hours but there were no differences between the groups. Bronchial responsiveness was not affected by IL-5. Conclusion - The effects of IL-5 appear to be mainly in the circulation, inducing peripheral mobilisation of eosinophils to the circulation without any effect on eosinophil mobilisation in the lungs or on bronchial responsiveness.
AB - Background - Interleukin 5 (IL-5) has an important role in mobilisation of eosinophils from the bone marrow and in their subsequent terminal differentiation. A study was undertaken to determine whether inhaled and intravenous IL-5 could induce pulmonary eosinophilia and bronchial hyperresponsiveness (BHR) independently of these effects. Methods - Nine mild asthmatics received inhaled (15 μg) or intravenous (2 μg) IL-5 or placebo in random order in a double blind, crossover study. Blood samples were taken before and at 0.5, 1, 2, 3, 4, 5, 24, and 72 hours following IL-5 or placebo, and bronchial responsiveness (PC20 methacholine) and eosinophil counts in induced sputum were determined. Results - Serum IL-5 levels were markedly increased 30 minutes after intravenous IL-5 (p=0.002), and sputum IL-5 levels increased 4 and 24 hours after inhaled IL-5 (p<0.05). Serum eotaxin was raised 24 hours after intravenous IL-5 but not after inhaled IL-5 or placebo. Blood eosinophils were markedly reduced 0.5-2 hours after intravenous IL-5 (p<0.05), followed by an increase at 3, 4, 5, and 72 hours (p<0.05). Sputum eosinophils rose significantly in all three groups at 24 hours but there were no differences between the groups. Bronchial responsiveness was not affected by IL-5. Conclusion - The effects of IL-5 appear to be mainly in the circulation, inducing peripheral mobilisation of eosinophils to the circulation without any effect on eosinophil mobilisation in the lungs or on bronchial responsiveness.
KW - Asthma
KW - Bronchial responsiveness
KW - Eosinophil
KW - Interleukin 5
UR - http://www.scopus.com/inward/record.url?scp=0035184832&partnerID=8YFLogxK
U2 - 10.1136/thorax.56.12.935
DO - 10.1136/thorax.56.12.935
M3 - Article
C2 - 11713356
AN - SCOPUS:0035184832
SN - 0040-6376
VL - 56
SP - 935
EP - 940
JO - Thorax
JF - Thorax
IS - 12
ER -