Safety of anti‐immunoglobulin E therapy with omalizumab in allergic patients at risk of geohelminth infection
Open Access
- 23 January 2007
- journal article
- research article
- Published by Wiley in Clinical and Experimental Allergy
- Vol. 37 (2) , 197-207
- https://doi.org/10.1111/j.1365-2222.2007.02650.x
Abstract
Although the role of immunoglobulin E (IgE) in immunity against helminth parasites is unclear, there is concern that therapeutic antibodies that neutralize IgE (anti-IgE) may be unsafe in subjects at risk of helminth infection. We conducted an exploratory study to investigate the safety of omalizumab (anti-IgE) in subjects with allergic asthma and/or perennial allergic rhinitis at high risk of intestinal helminth infection. The primary safety outcome was risk of infections with intestinal helminths during anti-IgE therapy. A randomized, double-blind, placebo-controlled trial was conducted in 137 subjects (12-30 years) at high risk of geohelminth infection. All subjects received pre-study anthelmintic treatment, followed by 52 weeks' treatment with omalizumab or placebo. Of the omalizumab subjects 50% (34/68) experienced at least one intestinal geohelminth infection compared with 41% (28/69) of placebo subjects [odds ratio (OR) 1.47, 95% confidence interval (CI) 0.74-2.95, one-sided P=0.14; OR (adjusted for study visit, baseline infection status, gender and age) 2.2 (0.94-5.15); one-sided P=0.035], providing some evidence for a potential increased incidence of geohelminth infection in subjects receiving omalizumab. Omalizumab therapy was well tolerated, and did not appear to be associated with increased morbidity attributable to intestinal helminths as assessed by clinical and laboratory adverse events, maximal helminth infection intensities and additional anthelmintic requirements. Time to first infection (OR 1.30, 95% CI 0.79-2.15, one-sided P=0.15) was similar between treatment groups. Infection severity and response to anthelmintics appeared to be unaffected by omalizumab therapy. In this exploratory study of allergic subjects at high risk of helminth infections, omalizumab therapy appeared to be safe and well tolerated, but may be associated with a modest increase in the incidence of geohelminth infection.Keywords
This publication has 26 references indexed in Scilit:
- Interleukin‐4‐ and interleukin‐13‐mediated host protection against intestinal nematode parasitesImmunological Reviews, 2004
- Focus: Soil-transmitted helminthiasisNature Reviews Microbiology, 2004
- Strongyloides stercoralisin the Immunocompromised PopulationClinical Microbiology Reviews, 2004
- Evaluation of long-term safety of the anti-IgE antibody, omalizumab, in children with allergic asthmaAnnals of Allergy, Asthma & Immunology, 2003
- Omalizumab is effective in the long-term control of severe allergic asthmaAnnals of Allergy, Asthma & Immunology, 2003
- Omalizumab, anti-IgE recombinant humanized monoclonal antibody, for the treatment of severe allergic asthmaJournal of Allergy and Clinical Immunology, 2001
- AnthelminticsDrugs, 1997
- IgE, allergies and helminth parasites: A new perspective on an old conundrumImmunology & Cell Biology, 1996
- Parasites and allergy: evidence for a ‘cause and effect’ relationshipClinical and Experimental Allergy, 1990