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Randomized controlled trial of high-dose sublingual immunotherapy to treat seasonal allergic rhinitis

Randomized controlled trial of high-dose sublingual immunotherapy to treat seasonal allergic rhinitis
Randomized controlled trial of high-dose sublingual immunotherapy to treat seasonal allergic rhinitis
Background: Seasonal allergic rhinitis is common and troublesome. Sublingual immunotherapy (SLIT) has been proposed as an alternative to injection immunotherapy and might offer some advantages if it were effective and practical in a community setting.
Objectives: To assess the efficacy and side-effect profile of SLIT in patients with summer hay fever uncontrolled on current standard medication. To assess the feasibility of delivering SLIT in a United Kingdom general practice setting.
Methods: Double-blind, placebo-controlled study in 186 patients with severe summer hay fever identified from 16 United Kingdom general practices. After a baseline year to ensure balanced groups, subjects were randomized, and SLIT was given for 1 or 2 years and compared with placebo. The principal outcome measure was symptoms as recorded on diary cards. Secondary criteria were skin and conjunctival reactivity, allergen-specific IgE and IgG4, and the frequency and severity of adverse effects.
Results: One hundred thirty-six subjects completed the study. After 1 year, no significant differences were found between actively treated subjects and the placebo group. After the second year of therapy, subjects who had received 2 years treatment were 6.8 times more likely to show a reduction in nose running (P < .001) and 2.4 times more likely to have reduced sneezing (P < .05) compared with subjects in the placebo group. Benefits for nasal blockage were found at the peak pollen season and were similar in both actively treated groups.
Conclusion: Sublingual immunotherapy can be given successfully and safely in the community. High-dose SLIT has beneficial effects on nasal symptoms during the peak pollen season in patients with severe seasonal allergic rhinitis. At least 2 years of treatment with SLIT is required to show a benefit.
sublingual immunotherapy, immunotherapy, seasonal allergic rhinitis, grass pollen, hay fever
0091-6749
831-837
Smith, Helen
42562879-cabb-497a-9209-ae8c6530b37d
White, Peter
536aaa93-447f-4103-ba6b-d424b51a5572
Annila, Ilkka
07932622-7eec-4883-9db8-466d13773e70
Poole, Jason
88c69acd-8ff1-4d82-bd3d-8ea1720557e1
Andre, Claude
3cd25db7-473d-406c-a5d3-141966797b08
Frew, Anthony
34641087-1d96-4c8e-9385-0d0dedbf0710
Smith, Helen
42562879-cabb-497a-9209-ae8c6530b37d
White, Peter
536aaa93-447f-4103-ba6b-d424b51a5572
Annila, Ilkka
07932622-7eec-4883-9db8-466d13773e70
Poole, Jason
88c69acd-8ff1-4d82-bd3d-8ea1720557e1
Andre, Claude
3cd25db7-473d-406c-a5d3-141966797b08
Frew, Anthony
34641087-1d96-4c8e-9385-0d0dedbf0710

Smith, Helen, White, Peter, Annila, Ilkka, Poole, Jason, Andre, Claude and Frew, Anthony (2004) Randomized controlled trial of high-dose sublingual immunotherapy to treat seasonal allergic rhinitis. Journal of Allergy and Clinical Immunology, 114 (4), 831-837. (doi:10.1016/j.jaci.2004.06.058).

Record type: Article

Abstract

Background: Seasonal allergic rhinitis is common and troublesome. Sublingual immunotherapy (SLIT) has been proposed as an alternative to injection immunotherapy and might offer some advantages if it were effective and practical in a community setting.
Objectives: To assess the efficacy and side-effect profile of SLIT in patients with summer hay fever uncontrolled on current standard medication. To assess the feasibility of delivering SLIT in a United Kingdom general practice setting.
Methods: Double-blind, placebo-controlled study in 186 patients with severe summer hay fever identified from 16 United Kingdom general practices. After a baseline year to ensure balanced groups, subjects were randomized, and SLIT was given for 1 or 2 years and compared with placebo. The principal outcome measure was symptoms as recorded on diary cards. Secondary criteria were skin and conjunctival reactivity, allergen-specific IgE and IgG4, and the frequency and severity of adverse effects.
Results: One hundred thirty-six subjects completed the study. After 1 year, no significant differences were found between actively treated subjects and the placebo group. After the second year of therapy, subjects who had received 2 years treatment were 6.8 times more likely to show a reduction in nose running (P < .001) and 2.4 times more likely to have reduced sneezing (P < .05) compared with subjects in the placebo group. Benefits for nasal blockage were found at the peak pollen season and were similar in both actively treated groups.
Conclusion: Sublingual immunotherapy can be given successfully and safely in the community. High-dose SLIT has beneficial effects on nasal symptoms during the peak pollen season in patients with severe seasonal allergic rhinitis. At least 2 years of treatment with SLIT is required to show a benefit.

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More information

Submitted date: 17 November 2003
Published date: October 2004
Keywords: sublingual immunotherapy, immunotherapy, seasonal allergic rhinitis, grass pollen, hay fever

Identifiers

Local EPrints ID: 27434
URI: http://eprints.soton.ac.uk/id/eprint/27434
ISSN: 0091-6749
PURE UUID: 812f386b-e8ca-40af-adc7-aa1f26fb05c8

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Date deposited: 26 Apr 2006
Last modified: 15 Mar 2024 07:18

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Contributors

Author: Helen Smith
Author: Peter White
Author: Ilkka Annila
Author: Jason Poole
Author: Claude Andre
Author: Anthony Frew

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