Editorial
Monitoring Allergic Patients on Omalizumab with Free and Total Serum IgE Measurements

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      The Th2 cytokines IL-4 and IL-13 activate class-switch recombination of IgM to produce elevated levels of IgE. Anti-IgE immunotherapy is effective treatment in patients with allergic asthma, though monitoring serum IgE levels in evaluating response to therapy is not routinely recommended [15]. IgE also cannot be used to predict asthma disease severity [16].

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      Finally, omalizumab (therapeutic anti-IgE) differentially influences the accuracy of multiple IgE antibody assays.39 Difficulties in accurately measuring total serum IgE after omalizumab administration remains problematic even with so-called free IgE assay methods.40 Finally, high levels of allergen-specific IgG antibody blocking induced after chronic natural or immunotherapy-induced allergen exposure can block IgE antibody binding to allergosorbents, especially on microchips such as the Immunosorbent Allergen Chip (ISAC) where the allergen density is limited.41,42

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      A Spanish consensus study was published and some criteria have been established to improve AIT prescription in poly-sensitized patients helping allergists to better identify relevant allergens in this kind of patients and to improve selection of AIT in each case.173 The use of the anti-IgE omalizumab to increase the efficacy and safety of AIT has been described in several studies with pollens, Hymenoptera venoms and food174–183 (level of evidence 1a, grade of recommendation A). AIT is administered in two phases: the initial build-up phase, when the dose and concentration of the extract is increased and the maintenance phase with fixed, optimal and maximum dose during intervals of between 4 and 6 weeks.

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    Conflicts of interest: R. G. Hamilton declares no relevant conflicts of interest.

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