Ultra‐short‐course booster is effective in recurrent grass pollen‐induced allergic rhinoconjunctivitis

Background A relevant proportion of allergic rhinoconjunctivitis (ARC) patients experience recurrent symptoms after successfully completing allergen immunotherapy (AIT). This prospective, controlled, noninterventional study used internationally standardized instruments to determine the clinical effe...

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Veröffentlicht in:Allergy (Copenhagen) 2018-01, Vol.73 (1), p.187-195
Hauptverfasser: Pfaar, O., Lang, S., Pieper‐Fürst, U., Astvatsatourov, A., Gerich, F., Klimek, L., Kramer, M. F., Reydelet, Y., Shah‐Hosseini, K., Mösges, R.
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Sprache:eng
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Zusammenfassung:Background A relevant proportion of allergic rhinoconjunctivitis (ARC) patients experience recurrent symptoms after successfully completing allergen immunotherapy (AIT). This prospective, controlled, noninterventional study used internationally standardized instruments to determine the clinical effects of a preseasonal, ultra‐short‐course booster AIT on clinical outcome parameters. Methods This two‐arm study included patients aged ≥12 years with recurrent grass pollen‐induced seasonal AR who had completed a successful course of any grass pollen AIT at least 5 years before enrolment. Overall, 56 patients received one preseasonal short‐course booster AIT using tyrosine‐absorbed grass pollen allergoids containing the adjuvant monophosphoryl lipid A (MPL®); 51 control patients received symptomatic medication. The combined symptom and medication score (CSMS) was recorded in the (peak) grass pollen season. Furthermore, concomitant (antiallergic) medication use, the patients’ state of health, Mini Rhinoconjunctivitis Quality of Life Questionnaire (MiniRQLQ) results and safety/tolerability of the treatment were assessed. Results The CSMS in the peak grass pollen season was significantly lower in the booster AIT group (Δ=38.4%, P
ISSN:0105-4538
1398-9995
DOI:10.1111/all.13240