House dust mite sublingual immunotherapy: Results of a US trial

被引:53
作者
Bush, Robert K. [1 ,2 ]
Swenson, Cheri [1 ]
Fahlberg, Beth [1 ]
Evans, Michael D. [3 ]
Esch, Robert [4 ]
Busse, William W. [1 ]
机构
[1] Univ Wisconsin, Sect Allergy Immunol Pulm Crit Care & Sleep Med, Madison, WI USA
[2] William S Middleton VA Hosp, Madison, WI USA
[3] Univ Wisconsin, Dept Biostat & Med Informat, Madison, WI USA
[4] Greer Labs, Res & Dev, Lenoir, NC USA
关键词
Sublingual immunotherapy; immunotherapy; house dust mites; Dermatophagoides farinae; house dust mite allergy; DOUBLE-BLIND; ALLERGIC RHINITIS; SWALLOW IMMUNOTHERAPY; PEDIATRIC-PATIENTS; CLINICAL-TRIALS; GRASS-POLLEN; ASTHMA; EFFICACY; CHILDREN; METAANALYSIS;
D O I
10.1016/j.jaci.2010.11.045
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Few trials of sublingual immunotherapy (SLIT) in the United States have been reported. Objective: This randomized, placebo-controlled feasibility SLIT study compared the safety and physiologic effects of high-versus low-dose Dermatophagoides farinae vaccine. Methods: Thirty-one D farinae-sensitive adults with allergic rhinitis with or without mild intermittent asthma were eligible for randomization to high-dose maintenance vaccine (n = 10, 4200 allergen units [approximately 70 mu g of Der f 1/d]), low-dose maintenance vaccine (n = 10; 60 allergen units [approximately 1 mu g of Der f 1/d]), or placebo (n = 11) over 12 to 18 months. Medication-symptom scores and adverse events were monitored, serum D farinae-specific IgE and IgG4 levels were measured, and bronchial reactivity to D farinae was determined at baseline and 6-month intervals. Results: Of the 31 randomized subjects, 6 withdrew because of non-treatment-ascribed events. Four withdrew because of treatment-ascribed effects: high-dose group, 1 of 10 (gastrointestinal symptoms); low-dose group, 1 of 10 (gastrointestinal symptoms); and placebo group, 2 of 11 (headache and increased nasal symptoms). Thus 21 subjects completed the study: high-dose group, 9; low-dose group, 7; and placebo group, 5. Eleven of the 21 subjects experienced mild-to-moderate gastrointestinal symptoms, throat irritation, or both (high-dose group, 5/9; low-dose group, 4/7; and placebo group, 2/5). No severe systemic reactions were noted. No differences in symptom-medication scores were found. High-dose SLIT increased the bronchial threshold to allergen challenge and increased serum D farinae-specific IgG4 levels, whereas low-dose SLIT and placebo had no significant effect. Conclusions: High-dose D farinae SLIT was generally tolerable, increased serum D farinae-specific IgG4 levels, and improved the bronchial threshold to allergen challenge. Larger US trials are warranted. (J Allergy Clin Immunol 2011;127:974-81.)
引用
收藏
页码:974 / U225
页数:15
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