Demonstration of two distinct antigenic determinants on hepatitis B e antigen by monoclonal antibodies.

  • M Imai
    Immunology Division, Jichi Medical School; the Hepatitis Division, the Tokyo Metropolitan Institute of Medical Science, University of Tokyo ,
  • M Nomura
    Immunology Division, Jichi Medical School; the Hepatitis Division, the Tokyo Metropolitan Institute of Medical Science, University of Tokyo ,
  • T Gotanda
    Immunology Division, Jichi Medical School; the Hepatitis Division, the Tokyo Metropolitan Institute of Medical Science, University of Tokyo ,
  • T Sano
    Immunology Division, Jichi Medical School; the Hepatitis Division, the Tokyo Metropolitan Institute of Medical Science, University of Tokyo ,
  • K Tachibana
    Immunology Division, Jichi Medical School; the Hepatitis Division, the Tokyo Metropolitan Institute of Medical Science, University of Tokyo ,
  • H Miyamoto
    Immunology Division, Jichi Medical School; the Hepatitis Division, the Tokyo Metropolitan Institute of Medical Science, University of Tokyo ,
  • K Takahashi
    Immunology Division, Jichi Medical School; the Hepatitis Division, the Tokyo Metropolitan Institute of Medical Science, University of Tokyo ,
  • S Toyama
    Immunology Division, Jichi Medical School; the Hepatitis Division, the Tokyo Metropolitan Institute of Medical Science, University of Tokyo ,
  • Y Miyakawa
    Immunology Division, Jichi Medical School; the Hepatitis Division, the Tokyo Metropolitan Institute of Medical Science, University of Tokyo ,
  • M Mayumi
    Immunology Division, Jichi Medical School; the Hepatitis Division, the Tokyo Metropolitan Institute of Medical Science, University of Tokyo ,

書誌事項

公開日
1982-01-01
権利情報
  • https://academic.oup.com/pages/standard-publication-reuse-rights
DOI
  • 10.4049/jimmunol.128.1.69
公開者
Oxford University Press (OUP)

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説明

<jats:title>Abstract</jats:title> <jats:p>Mice were immunized against hepatitis B e antigen (HBeAg) isolated from sera of asymptomatic carriers of hepatitis B virus. Their spleen cells were fused with mouse myeloma (NS-1) cells, and 5 clones of hybridoma cells secreting antibody against HBeAg (anti-HBe) were isolated. For the production of anti-HBe in large scale, cells were cultivated both in vitro and in the peritoneal cavity of ascitic mice. Although monoclonal antibodies produced by these clones showed a strong reactivity of anti-HBe in hemagglutination tests, individual monoclonal anti-HBe did not reveal any precipitin line in immunodiffusion. When 2 of the 5 monoclonal antibodies were mixed together, however, some combinations showed a precipitin line against HBeAg, whereas others did not. Utilizing solid-phase radioimmunoassay involving a number of combinations of monoclonal antibodies used for solid-phase and radiolabeling, the 5 antibodies were classified into 2 groups. Three of the anti-HBe antibodies were found to be directed to 1 determinant of HBeAg (determinant a); the remaining 2 to the other determinant (determinant b). Determinants a and b were detected on HBeAg in the serum, as well as on the polypeptide of 19,000 daltons (P19) derived from the nucleocapsid of hepatitis B virus. Monoclonal anti-HBe antibodies with different specificities may provide useful tools in delineating the antigenic structure of HBeAg and also in evaluating immune responses of the host directed to its subdeterminants.</jats:p>

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