Mj. Leckie et al., Effects of an interleukin-5 blocking monoclonal antibody on eosinophils, airway hyper-responsiveness, and the late asthmatic response, LANCET, 356(9248), 2000, pp. 2144-2148
Citations number
34
Categorie Soggetti
General & Internal Medicine","Medical Research General Topics
Background Interleukin-5 (IL-5) is essential for the formation of eosinophi
ls, which are thought to have a major role in the pathogenesis of asthma an
d other allergic diseases. We aimed to assess the effects of monoclonal ant
ibody to IL-5 on blood and sputum eosinophils, airway hyperresponsiveness,
and the late asthmatic reaction to inhaled allergen in patients with mild a
sthma.
Methods We did a double-blind randomised placebo-controlled trial, in which
a single intravenous infusion of humanised (IgG-kappa) monoclonal antibody
to IL-5 (SB-240563) was given at doses of 2 .5 mg/kg (n=8) or 10 .0 mg/kg
(n=8). The effects of treatment on responses to inhaled allergen challenge,
sputum eosinophils, and airway hyper-responsiveness to histamine were meas
ured at weeks 1 and 4 with monitoring of blood eosinophil counts for up to
16 weeks.
Findings Monoclonal antibody against IL-5 towered the mean blood eosinophil
count at day 29 from 0 . 25x10(9)/L (95% Cl 0 . 16-0 . 34) in the placebo
group to 0 . 04x10(9)/L (0 . 00-0 . 07) in the 10 mg/kg group (p<0<bullet>0
001), and prevented the blood eosinophilia that follows allergen challenge.
After inhaled allergen challenge, 9 days after treatment, the percentage s
putum eosinophils were 12 .2% in the placebo group and lowered to 0 .9% (-1
.2 to 3 .0; p=0 . 0076) in the 10 mg/kg group, and this effect persisted a
t day 30 after the dose. There was no significant effect of monoclonal anti
body to IL-5 on the late asthmatic response or on airway hyperresponsivenes
s to histamine.
Interpretation A single dose of monoclonal antibody to IL-5 decreased blood
eosinophils for up to 16 weeks and sputum eosinophils at 4 weeks, which ha
s considerable therapeutic potential for asthma and allergy. However, our f
indings question the role of eosinophils in mediating the late asthmatic re
sponse and causing airway hyper-responsiveness.