Hierarchical suppression of asthma-like responses by mucosal tolerance

Mucosal tolerance can be induced by oral or nasal administration of soluble proteins and results in the suppression of cellular and/or humoral immune responses to the specific antigen. To compare the effect of oral or nasal ovalbumin administration before, during or after immunization on the develop...

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Veröffentlicht in:Journal of Allergy and Clinical Immunology 2006-02, Vol.117 (2), p.283-290
Hauptverfasser: Keller, Alexandre C., Mucida, Daniel, Gomes, Eliane, Faquim-Mauro, Eliana, Faria, Ana Maria Caetano, Rodriguez, Dunia, Russo, Momtchilo
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container_end_page 290
container_issue 2
container_start_page 283
container_title Journal of Allergy and Clinical Immunology
container_volume 117
creator Keller, Alexandre C.
Mucida, Daniel
Gomes, Eliane
Faquim-Mauro, Eliana
Faria, Ana Maria Caetano
Rodriguez, Dunia
Russo, Momtchilo
description Mucosal tolerance can be induced by oral or nasal administration of soluble proteins and results in the suppression of cellular and/or humoral immune responses to the specific antigen. To compare the effect of oral or nasal ovalbumin administration before, during or after immunization on the development of cellular and humoral immune responses by using a murine asthma model. To induce lung allergic inflammation, animals were immunized twice with ovalbumin/aluminum hydroxide gel and challenged twice with ovalbumin. To induce tolerance, BALB/c mice received ovalbumin by the oral or nasal routes for 3 consecutive days. The ovalbumin administration was initiated before (day –7), during (day 0), or after immunization (day 7). Airway eosinophilia, airway hyperreactivity, mucus hypersecretion, and cytokine production were suppressed when oral or nasal ovalbumin administration was initiated before immunization. Oral but not nasal ovalbumin exposure suppressed ovalbumin-specific nonanaphylactic IgG 1 antibodies, whereas both routes suppressed the production of anaphylactic IgG 1 and IgE antibodies. Mucosal ovalbumin administration at day 0 inhibited all T H2-mediated allergic parameters but not nonanaphylactic IgG 1 antibodies. Finally, ovalbumin exposure 7 days after immunization was still effective in suppressing lung allergy but not ovalbumin-specific anaphylactic IgG 1 and IgE antibodies. We show that the effectiveness of mucosal tolerance depends on route and time and presents a hierarchical pattern of suppression in the following order: lung allergic responses > anaphylactic antibodies > ovalbumin-specific IgG 1.
doi_str_mv 10.1016/j.jaci.2005.10.019
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To compare the effect of oral or nasal ovalbumin administration before, during or after immunization on the development of cellular and humoral immune responses by using a murine asthma model. To induce lung allergic inflammation, animals were immunized twice with ovalbumin/aluminum hydroxide gel and challenged twice with ovalbumin. To induce tolerance, BALB/c mice received ovalbumin by the oral or nasal routes for 3 consecutive days. The ovalbumin administration was initiated before (day –7), during (day 0), or after immunization (day 7). Airway eosinophilia, airway hyperreactivity, mucus hypersecretion, and cytokine production were suppressed when oral or nasal ovalbumin administration was initiated before immunization. Oral but not nasal ovalbumin exposure suppressed ovalbumin-specific nonanaphylactic IgG 1 antibodies, whereas both routes suppressed the production of anaphylactic IgG 1 and IgE antibodies. 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To compare the effect of oral or nasal ovalbumin administration before, during or after immunization on the development of cellular and humoral immune responses by using a murine asthma model. To induce lung allergic inflammation, animals were immunized twice with ovalbumin/aluminum hydroxide gel and challenged twice with ovalbumin. To induce tolerance, BALB/c mice received ovalbumin by the oral or nasal routes for 3 consecutive days. The ovalbumin administration was initiated before (day –7), during (day 0), or after immunization (day 7). Airway eosinophilia, airway hyperreactivity, mucus hypersecretion, and cytokine production were suppressed when oral or nasal ovalbumin administration was initiated before immunization. Oral but not nasal ovalbumin exposure suppressed ovalbumin-specific nonanaphylactic IgG 1 antibodies, whereas both routes suppressed the production of anaphylactic IgG 1 and IgE antibodies. Mucosal ovalbumin administration at day 0 inhibited all T H2-mediated allergic parameters but not nonanaphylactic IgG 1 antibodies. Finally, ovalbumin exposure 7 days after immunization was still effective in suppressing lung allergy but not ovalbumin-specific anaphylactic IgG 1 and IgE antibodies. 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Mucosal ovalbumin administration at day 0 inhibited all T H2-mediated allergic parameters but not nonanaphylactic IgG 1 antibodies. Finally, ovalbumin exposure 7 days after immunization was still effective in suppressing lung allergy but not ovalbumin-specific anaphylactic IgG 1 and IgE antibodies. We show that the effectiveness of mucosal tolerance depends on route and time and presents a hierarchical pattern of suppression in the following order: lung allergic responses &gt; anaphylactic antibodies &gt; ovalbumin-specific IgG 1.</abstract><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>16461128</pmid><doi>10.1016/j.jaci.2005.10.019</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Wiley Journals; Elsevier ScienceDirect Journals Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Wiley Free Content; IngentaConnect Free/Open Access Journals; PubMed Central
subjects Administration, Intranasal
Administration, Oral
AHR
Allergies
anaphylactic antibodies
Anaphylaxis - immunology
Animals
Asthma
Asthma - immunology
Asthma - physiopathology
Asthma - therapy
Biological and medical sciences
Breeding of animals
Bronchial Hyperreactivity - immunology
Bronchoalveolar Lavage Fluid - cytology
Bronchoalveolar Lavage Fluid - immunology
Chemokines
Cytokines
Disease Models, Animal
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Immune system
Immune Tolerance - immunology
Immunization
Immunoglobulin E - blood
Immunoglobulin G - blood
Immunopathology
Lymphocytes
Male
Medical sciences
Mice
Mice, Inbred BALB C
Mucous Membrane - immunology
Ovalbumin - administration & dosage
Pulmonary Eosinophilia - immunology
Rodents
Spleen
Time Factors
Tolerance
title Hierarchical suppression of asthma-like responses by mucosal tolerance
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