A randomized, double-blind, placebo-controlled pilot study of sublingual versus oral immunotherapy for the treatment of peanut allergy

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

卷:135

Article

Narisety, Satya D.¹  Frischmeyer-Guerrerio, Pamela A.²  Keet, Corinne A.²  Gorelik, Mark²  Schroeder, John³  Hamilton, Robert G.³  Wood, Robert A.² 

[1] Rutgers State Univ, New Jersey Med Sch, Dept Pediat, Div Allergy Immunol & Infect Dis, Newark, NJ 07102 USA

[2] Johns Hopkins Univ, Sch Med, Dept Pediat, Baltimore, MD 21205 USA

[3] Johns Hopkins Univ, Sch Med, Dept Med, Div Allergy & Immunol, Baltimore, MD 21205 USA

关键词: Peanut allergy;    food allergy;    immunotherapy;    sublingual immunotherapy;    oral immunotherapy;   

DOI  :  10.1016/j.jaci.2014.11.005

来源: Elsevier

【 摘 要 】

Background: Although promising results have emerged regarding oral immunotherapy (OIT) and sublingual immunotherapy (SLIT) for the treatment of peanut allergy (PA), direct comparisons of these approaches are limited. Objective: This study was conducted to compare the safety, efficacy, and mechanistic correlates of peanut OIT and SLIT. Methods: In this double-blind study children with PA were randomized to receive active SLIT/placebo OIT or active OIT/placebo SLIT. Doses were escalated to 3.7 mg/d (SLIT) or 2000 mg/d (OIT), and subjects were rechallenged after 6 and 12 months of maintenance. After unblinding, therapy was modified per protocol to offer an additional 6 months of therapy. Subjects who passed challenges at 12 or 18 months were taken off treatment for 4 weeks and rechallenged. Results: Twenty-one subjects aged 7 to 13 years were randomized. Five discontinued therapy during the blinded phase. Of the remaining 16, all had a greater than 10-fold increase in challenge threshold after 12 months. The increased threshold was significantly greater in the active OIT group (141-vs 22-fold, P = .01). Significant within-group changes in skin test results and peanut-specific IgE and IgG(4) levels were found, with overall greater effects with OIT. Adverse reactions were generally mild but more common with OIT (P < .001), including moderate reactions and doses requiring medication. Four subjects had sustained unresponsiveness at study completion. Conclusion: OIT appeared far more effective than SLIT for the treatment of PA but was also associated with significantly more adverse reactions and early study withdrawal. Sustained unresponsiveness after 4 weeks of avoidance was seen in only a small minority of subjects.

【 授权许可】

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