The effects of a monoclonal antibody directed against tumor necrosis factor-α in asthma

EM Erin, BR Leaker, GC Nicholson, AJ Tan… - American journal of …, 2006 - atsjournals.org
EM Erin, BR Leaker, GC Nicholson, AJ Tan, LM Green, H Neighbour, AS Zacharasiewicz…
American journal of respiratory and critical care medicine, 2006atsjournals.org
Rationale: Neutralization of tumor necrosis factor-α (TNF-α) is an effective antiinflammatory
therapy for several chronic inflammatory diseases. Methods and Objectives: We undertook a
double-blind, placebo-controlled, parallel-group design study in 38 patients with moderate
asthma treated with inhaled corticosteroids but symptomatic during a run-in phase.
Infliximab (5 mg/kg) or placebo was administered by intravenous infusion at Weeks 0, 2, and
6. We assessed clinical response by monitoring lung function, symptoms, and inhaled β2 …
Rationale: Neutralization of tumor necrosis factor-α (TNF-α) is an effective antiinflammatory therapy for several chronic inflammatory diseases.
Methods and Objectives: We undertook a double-blind, placebo-controlled, parallel-group design study in 38 patients with moderate asthma treated with inhaled corticosteroids but symptomatic during a run-in phase. Infliximab (5 mg/kg) or placebo was administered by intravenous infusion at Weeks 0, 2, and 6. We assessed clinical response by monitoring lung function, symptoms, and inhaled β2-agonist usage using hand-held electronic devices.
Results: The primary endpoint, change in morning PEF at Days 50–56 compared with the last 7 d of the run-in, was not significantly different on treatment. However, infliximab was associated with a decrease in mean diurnal variation of PEF at Week 8 (p = 0.02; 95% confidence interval [CI], −8.1 to −0.72). Furthermore, there was a decrease in the number of patients with exacerbations of asthma (p = 0.01; 95% CI, 4.4 to 52.7) and an increased probability of freedom from exacerbation with time (p = 0.03) in patients on infliximab (n = 14) compared with placebo (n = 18). In addition, infliximab decreased levels of TNF-α (p = 0.01) and other cytokines in sputum supernatants. There were no serious adverse events related to the study agent.
Conclusions: Treatment with infliximab was well tolerated and caused a decrease in the number of patients with exacerbations in symptomatic moderate asthma. The promising preliminary findings underscore the need to evaluate therapy directed against TNF-α in larger trials enrolling patients with more severe asthma.
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