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Details

Autor(en) / Beteiligte
Titel
Selective ablation of mast cells or basophils reduces peanut-induced anaphylaxis in mice
Ist Teil von
  • Journal of allergy and clinical immunology, 2013-10, Vol.132 (4), p.881-888.e11
Ort / Verlag
New York, NY: Mosby, Inc
Erscheinungsjahr
2013
Link zum Volltext
Quelle
Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
Beschreibungen/Notizen
  • Background Studies with c- kit mutant mast cell (MC)–deficient mice and antibody-mediated depletion of basophils suggest that both MCs and basophils can contribute to peanut-induced anaphylaxis (PIA). However, interpretation of data obtained by using such approaches is complicated because c- kit mutant mice have several phenotypic abnormalities in addition to MC deficiency and because basophil-depleting antibodies can also react with MCs. Objective We analyzed (1) the changes in the features of PIA in mice after the selective and inducible ablation of MCs or basophils and (2) the possible importance of effector cells other than MCs and basophils in the PIA response. Methods Wild-type and various mutant mice were orally sensitized with peanut extract and cholera toxin weekly for 4 weeks and challenged intraperitoneally with peanut extract 2 weeks later. Results Peanut-challenged, MC-deficient Kit W-sh/W-sh mice had reduced immediate hypothermia, as well as a late-phase decrease in body temperature that was abrogated by antibody-mediated depletion of neutrophils. Diphtheria toxin–mediated selective depletion of MCs or basophils in Mcpt5-Cre ; iDTR and Mcpt8 DTR mice, respectively, and treatment of wild-type mice with the basophil-depleting antibody Ba103 significantly reduced peanut-induced hypothermia. Non–c- kit mutant MC- and basophil-deficient Cpa3-Cre;Mcl-1 fl/fl mice had reduced but still significant responses to peanut. Conclusion Inducible and selective ablation of MCs or basophils in non–c- kit mutant mice can significantly reduce PIA, but partial responses to peanut can still be observed in the virtual absence of both cell types. The neutrophilia in Kit W-sh/W-sh mice might influence the responses of these mice in this PIA model.
Sprache
Englisch
Identifikatoren
ISSN: 0091-6749, 1097-6825
eISSN: 1097-6825
DOI: 10.1016/j.jaci.2013.06.008
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3794715
Format
Schlagworte
Allergies, allergy, Allergy and Immunology, anaphylaxis, Anaphylaxis - etiology, Anaphylaxis - immunology, Anaphylaxis - metabolism, Anaphylaxis/etiology/immunology/metabolism, Animals, Antibodies - immunology, Antibodies - metabolism, Antibodies/immunology/metabolism, Arachis - immunology, Arachis hypogaea, Arachis hypogaea/immunology, basophils, Basophils - immunology, Basophils - metabolism, Basophils/immunology/metabolism, Biological and medical sciences, BMCMC, Bone marrow–derived cultured mast cell, Carboxypeptidase A3, Connective tissue–type mast cells, Cpa3, CTMC, Diphtheria toxin, Diphtheria Toxin - immunology, Diphtheria toxin receptor, DTR, Flow cytometry, Food, Food allergies, Fundamental and applied biological sciences. Psychology, Fundamental immunology, Immunopathology, Kit(W-sh/W-sh), KitW-sh/W-sh, Laboratories, Life sciences, Mast cell, Mast cell protease, mast cell protease 5, mast cells, Mast Cells - immunology, Mast Cells - metabolism, Mast Cells/immunology/metabolism, Mcpt, Medical sciences, Mice, Mice, Inbred C57BL, MMC, Mucosal mast cell, Mutation, neutrophils, PAF, Passive systemic anaphylaxis, Peanut, Peanut Hypersensitivity - complications, Peanut Hypersensitivity - immunology, Peanut Hypersensitivity - metabolism, Peanut Hypersensitivity/complications/immunology/metabolism, Peanut-induced anaphylaxis, PIA, Plasma, Platelet-activating factor, Proto-Oncogene Proteins c-kit - immunology, Proto-Oncogene Proteins c-kit - metabolism, Proto-Oncogene Proteins c-kit/immunology/metabolism, PSA, Rodents, Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis, Sciences du vivant, Wild-type

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