Type-I-hypersensitivity to 15 kDa, 28 kDa and 54 kDa proteins in vitellogenin specific to Gadus chalcogrammus roe

  • Hanaoka Keiko
    Department of Dermatology, Institute of Biomedical & Health Sciences, Hiroshima University
  • Takahagi Shunsuke
    Department of Dermatology, Institute of Biomedical & Health Sciences, Hiroshima University
  • Ishii Kaori
    Department of Dermatology, Institute of Biomedical & Health Sciences, Hiroshima University
  • Nakano Miyako
    Unit of Biotechnology, Graduate School of Integrated Sciences for Life, Hiroshima University
  • Chinuki Yuko
    Department of Dermatology, Shimane University Faculty of Medicine
  • Tanaka Akio
    Department of Dermatology, Institute of Biomedical & Health Sciences, Hiroshima University
  • Yanase Yuhki
    Department of Dermatology, Institute of Biomedical & Health Sciences, Hiroshima University
  • Hide Michihiro
    Department of Dermatology, Institute of Biomedical & Health Sciences, Hiroshima University

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  • Type-I-hypersensitivity to 15 kDa, 28 kDa and 54 kDa proteins in vitellogenin specific to <i>Gadus chalcogrammus</i> roe

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<p>Background: Fish roe allergy is a common health problem in countries where sea food is a major part of the diet, such as Japan. β′-component (β′-c) in fish roe has been identified as a major antigen for patients who show hypersensitivity to various fish roes. However, little is known about causative antigens for patients reactive to fish roe of specific species.</p><p>Methods: Serum and basophils were obtained from patients who had reactivity to roes of Gadus chalcogrammus (GC) and/or other fish species. GC roe specific antigens were analyzed by immunoblotting, histamine release assay (HRA) and mass spectrometry. Recombinant-fragments of vitellogenin (Vg) were obtained by the Escherichia coli expression system.</p><p>Results: Serum IgE of a patient with specific reactions to GC roe bound to 15, 28, 40 and 70 kDa-proteins in GC roe extract. Mass spectrometry analysis revealed that proteins in these bands contained fragments corresponding to Vg. Immunoblotting of Vg immunoprecipitated by rabbit anti-Vg antiserum from the extract revealed 15, 28 and 54 kDa fragments bound by the patient's IgE. These bindings were inhibited by the pretreatment of recombinant phosvitin (rPv) and β′-c (rβ′-c). Fractions obtained by native gel electrophoresis containing 15, 28 and 54 kDa proteins, but not the other fractions, induced significant histamine release from the patient's basophils. Sera of the other patients with GC roe specific-IgE showed IgE binding to rPv and/or rβ′-c.</p><p>Conclusions: The 15, 28 and 54 kDa-fragments of Vg which include structures of Pv and β′-c, could be antigens for GC roe specific type-I-hypersensitivity.</p>

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