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Repeated intranasal TLR7 stimulation reduces allergen responsiveness in allergic rhinitis
Authors:Lennart Greiff  Anders Cervin  Cecilia Ahlstr?m-Emanuelsson  Gun Almqvist  Morgan Andersson  Jan Dolata  Leif Eriksson  Edward H?gest?tt  Anders K?llén  Per Norlén  Inga-Lisa Sj?lin  Henrik Widegren
Institution:1.Department of ORL, Head & Neck Surgery, Skane University Hospital, Lund, Sweden;2.Department of ORL, Helsingborg Hospital, Helsingborg, Sweden;3.Research & Development, AstraZeneca, Lund, Sweden;4.Department of Clinical Pharmacology, Skane University Hospital, Lund, Sweden
Abstract:

Background

Interactions between Th1 and Th2 immune responses are of importance to the onset and development of allergic disorders. A Toll-like receptor 7 agonist such as AZD8848 may have potential as a treatment for allergic airway disease by skewing the immune system away from a Th2 profile.

Objective

To evaluate the efficacy and safety of intranasal AZD8848.

Methods

In a placebo-controlled single ascending dose study, AZD8848 (0.3-600 μg) was given intranasally to 48 healthy subjects and 12 patients with allergic rhinitis (NCT00688779). In a placebo-controlled repeat challenge/treatment study, AZD8848 (30 and 60 μg) was given once weekly for five weeks to 74 patients with allergic rhinitis out of season: starting 24 hours after the final dose, daily allergen challenges were given for seven days (NCT00770003). Safety, tolerability, pharmacokinetics, and biomarkers were monitored. During the allergen challenge series, nasal symptoms and lavage fluid levels of tryptase and α2-macroglobulin, reflecting mast cell activity and plasma exudation, were monitored.

Results

AZD8848 produced reversible blood lymphocyte reductions and dose-dependent flu-like symptoms: 30–100 μg produced consistent yet tolerable effects. Plasma interleukin-1 receptor antagonist was elevated after administration of AZD8848, reflecting interferon production secondary to TLR7 stimulation. At repeat challenge/treatment, AZD8848 reduced nasal symptoms recorded ten minutes after allergen challenge up to eight days after the final dose. Tryptase and α2-macroglobulin were also reduced by AZD8848.

Conclusions

Repeated intranasal stimulation of Toll-like receptor 7 by AZD8848 was safe and produced a sustained reduction in the responsiveness to allergen in allergic rhinitis.

Trial registration

NCT00688779 and NCT00770003 as indicated above.
Keywords:Allergy  Immunity  Seasonal  Toll-like receptor 7  Treatment
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