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Research Article Free access | 10.1172/JCI114266

Production of human monoclonal anti-basement membrane zone (BMZ) antibodies from a patient with bullous pemphigoid (BP) by Epstein-Barr virus transformation. Analyses of the heterogeneity of anti-BMZ antibodies in BP sera using them.

T Sugi, T Hashimoto, T Hibi, and T Nishikawa

Department of Dermatology, Keio University School of Medicine, Tokyo, Japan.

Find articles by Sugi, T. in: PubMed | Google Scholar

Department of Dermatology, Keio University School of Medicine, Tokyo, Japan.

Find articles by Hashimoto, T. in: PubMed | Google Scholar

Department of Dermatology, Keio University School of Medicine, Tokyo, Japan.

Find articles by Hibi, T. in: PubMed | Google Scholar

Department of Dermatology, Keio University School of Medicine, Tokyo, Japan.

Find articles by Nishikawa, T. in: PubMed | Google Scholar

Published October 1, 1989 - More info

Published in Volume 84, Issue 4 on October 1, 1989
J Clin Invest. 1989;84(4):1050–1055. https://doi.org/10.1172/JCI114266.
© 1989 The American Society for Clinical Investigation
Published October 1, 1989 - Version history
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Abstract

We established three lymphoblastoid cell lines from a bullous pemphigoid (BP) patient's peripheral blood by means of EBV transformation, which produced human monoclonal anti-basement membrane zone (BMZ) IgG antibodies. A blocking immunofluorescence test using these MAbs, designated 5A, 5E, and 10D, revealed that 5A and 5E recognized the same or a closely associated epitope, but the epitope for 10D was completely different, 18 of 30 BP sera blocked the reactivity of 10D MAb and 17 sera blocked 5E, while 9 sera did not block the staining of either antibody. Immunoblot analysis demonstrated that both 5A and 5E MAbs reacted exclusively with a protein band of approximately 230 kD in normal human epidermal extracts. However, 10D did not show any protein band. 22 of 30 BP sera strongly reacted with the same 230-kD protein, while none of control sera showed such reactivity. These results clearly demonstrated the heterogeneity of anti-BMZ antibodies in terms of epitopes. These MAbs should be useful in future investigations concerning not only the immunopathology but also the biochemial and molecular analyses of the BP antigen.

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