Short course of grass allergen peptides immunotherapy over 3 weeks reduces seasonal symptoms in allergic rhinoconjunctivitis with/without asthma: a randomized, multicenter, double-blind, placebo-controlled trial

BACKGROUND: Immunotherapy with peptide hydrolysates from Lolium perenne (LPP) is an alternative treatment for seasonal allergic rhinitis with or without asthma. The aim of this study was to assess the clinical efficacy and safety of a cumulative dose of 170 μg LPP administered subcutaneously over 3...

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Hauptverfasser: Mösges, Ralph (VerfasserIn) , Bachert, C. (VerfasserIn) , Panzner, P. (VerfasserIn) , Calderon, M. A. (VerfasserIn) , Haazen, L. (VerfasserIn) , Pirotton, S. (VerfasserIn) , Wathelet, N. (VerfasserIn) , Durham, S. R. (VerfasserIn) , Bonny, M.-A. (VerfasserIn) , Legon, T. (VerfasserIn) , von Frenckell, R. (VerfasserIn) , Pfaar, Oliver (VerfasserIn) , Shamji, M. H. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2018
In: Allergy
Year: 2018, Jahrgang: 73, Heft: 9, Pages: 1842-1850
ISSN:1398-9995
DOI:10.1111/all.13433
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1111/all.13433
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Verfasserangaben:R. Mösges, C. Bachert, P. Panzner, M.A. Calderon, L. Haazen, S. Pirotton, N. Wathelet, S. R. Durham, M.-A. Bonny, T. Legon, R. von Frenckell, O. Pfaar, M.H. Shamji

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520 |a BACKGROUND: Immunotherapy with peptide hydrolysates from Lolium perenne (LPP) is an alternative treatment for seasonal allergic rhinitis with or without asthma. The aim of this study was to assess the clinical efficacy and safety of a cumulative dose of 170 μg LPP administered subcutaneously over 3 weeks. - METHODS: In a randomized, double-blind, placebo-controlled trial, 554 adults with grass pollen rhinoconjunctivitis were randomized (1:2 ratio) to receive 8 subcutaneous injections of placebo or 170 μg LPP administered in increasing doses in 4 visits over 3 weeks. The primary outcome was the combined symptom and medication score (CSMS) measured over the peak pollen season. Reactivity to conjunctival provocation test (CPT) and quality of life (QOL) was assessed as secondary endpoints. - RESULTS: The mean reduction in CSMS in the LPP vs placebo group was -15.5% (P = .041) during the peak period and -17.9% (P = .029) over the entire pollen season. LPP-treated group had a reduced reactivity to CPT (P < .001) and, during the pollen season, a lower rhinoconjunctivitis QOL global score (P = .005) compared with placebo group. Mostly mild and WAO grade 1 early systemic reaction (ESR) were observed ≤30 minutes in 10.5% of LPP-treated patients, whereas 3 patients with a medical history of asthma (<1%) experienced a serious ESR that resolved with rescue medication. - CONCLUSION: Lolium perenne pollen peptides administered over 3 weeks before the grass pollen season significantly reduced seasonal symptoms and was generally safe and well-tolerated. 
650 4 |a Allergens 
650 4 |a Asthma 
650 4 |a Case-Control Studies 
650 4 |a clinical trial 
650 4 |a Desensitization, Immunologic 
650 4 |a Drug Administration Schedule 
650 4 |a Female 
650 4 |a grass pollen 
650 4 |a Humans 
650 4 |a Lolium perenne 
650 4 |a Male 
650 4 |a peptide immunotherapy 
650 4 |a Peptides 
650 4 |a Poaceae 
650 4 |a Pollen 
650 4 |a Quality of Life 
650 4 |a Rhinitis, Allergic, Seasonal 
650 4 |a Seasons 
650 4 |a subcutaneous immunotherapy 
650 4 |a Treatment Outcome 
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