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IL-18 Does not Increase Allergic Airway Disease in Mice When Produced by BCG
Author(s) -
L. Amniai,
Franck Biet,
Philippe Marquillies,
Camille Locht,
Joël Pestel,
AndréBernard Tonnel,
Catherine Duez
Publication year - 2007
Publication title -
journal of biomedicine and biotechnology
Language(s) - English
Resource type - Journals
eISSN - 1110-7251
pISSN - 1110-7243
DOI - 10.1155/2007/67276
Subject(s) - ovalbumin , immunology , medicine , eosinophil , context (archaeology) , intraperitoneal injection , immunization , cytokine , mucus , allergen , allergy , asthma , biology , immune system , pharmacology , paleontology , ecology
Whilst BCG inhibits allergic airway responses in murine models, IL-18 has adversary effects depending on its environment. We therefore constructed a BCG strain producing murine IL-18 (BCG-IL-18) and evaluated its efficiency to prevent an asthma-like reaction in mice.BALB/cByJ mice were sensitized (day (D) 1 and D10) by intraperitoneal injection of ovalbumin (OVA)-alum and primary (D2022) and secondary (D62, 63) challenged with OVA aerosols. BCG or BCG-IL-18 were intraperitonealy administered 1 hour before each immunization (D1 and D10). BCG-IL-18 and BCG were shown to similarly inhibit the development of AHR, mucus production, eosinophil influx, and local Th2 cytokine production in BAL, both after the primary and secondary challenge.These data show that IL-18 did not increase allergic airway responses in the context of the mycobacterial infection, and suggest that BCG-IL-18 and BCG are able to prevent the development of local Th2 responses and therefore inhibit allergen-induced airway responses even after restimulation

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