Oral Mucosal Immunotherapy for Allergic Rhinitis: A Pilot Study

Author:

Reisacher William R.1,Suurna Maria V.1,Rochlin Kate2,Bremberg Maria G.1,Tropper Guy3

Affiliation:

1. Department of Otolaryngology—Head and Neck Surgery, Weill Cornell Medical College, New York, NY

2. Department of Cell Biology, Weill Cornell Medical College, New York, NY

3. Avant Garde Médical, Boucherville, Quebec, Canada Supported by research grants from the New York State Office of Science, Technology and Academic Research, Allovate and the American Academy of Otolaryngic Allergy Foundation. Grantors played no other roles.

Abstract

Background The sublingual mucosa has been used for many years to apply allergenic extracts for the purpose of specific immunotherapy (IT). Although sublingual IT (SLIT) is both safe and efficacious, the density of antigen-presenting cells is higher in other regions of the oral cavity and vestibule, which make them a potentially desirable target for IT. Objective To present the concept of oral mucosal IT (OMIT) and to provide pilot data for this extended application of SLIT. Methods An open-label, 12-month, prospective study was undertaken as a preliminary step before a full-scale clinical investigation. Twenty-four individuals with allergic rhinitis received IT by applying allergenic extracts daily to either the oral vestibule plus oral cavity mucosa by using a glycerin-based toothpaste or to the sublingual mucosa by using 50% glycerin liquid drops. Adverse events, adherence rates, total combined scores, rhinoconjunctivitis quality-of-life questionnaire scores, changes in skin reactivity, and changes in serum antibody levels were measured for each participant. Results No severe adverse events occurred in either group. The adherence rate was 80% for the OMIT group and 62% for the SLIT group (p = 0.61). Decreased total combined scores were demonstrated for both the OMIT group (15.6%) and the SLIT group (223%), although this decrease did not reach statistical significance in either group. Both groups achieved a meaningful clinical improvement of at least 0.5 points on rhinoconjunctivitis quality-of-life questionnaire. A statistically significant rise in specific immunoglobulin G4 (IgG4) was seen in both groups over the first 6 months of treatment. Conclusion OMIT and SLIT demonstrated similar safety profiles and adherence rates. Measurements of clinical efficacy improved for both groups, but only changes in IgG4 achieved statistical significance. These pilot data provide enough evidence to proceed with a full-scale investigation to explore the role of OMIT in the long-term management of allergic rhinitis.

Publisher

SAGE Publications

Subject

Otorhinolaryngology,Immunology and Allergy

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