Abstract
Serum from patients with type I diabetes mellitus contains antibodies which react with all islet cells on sections of human pancreas1, normal rat islet cell surface antigens2, antigens expressed by islet cell tumours3, β-cell-specific surface antigens4 and A cells of sections of human pancreas5. Due in part to the low titre of anti-islet antibodies, the biochemistry of the relevant islet cell antigens is poorly understood6. Our laboratory has begun to develop and define a series of murine monoclonal anti-islet antibodies7–9. In addition, we have begun to explore the possibility of producing human hybridomas secreting monoclonal anti-islet antibodies by fusing lymphocytes from patients having type I diabetes mellitus with human myeloma cell lines. We describe here the isolation of human hybridomas that secrete human monoclonal anti-islet antibody. The availability of hybridoma clones secreting autoantibody should result in a better understanding of the mechanisms resulting in the expression of human autoantibodies.
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Eisenbarth, G., Linnenbach, A., Jackson, R. et al. Human hybridomas secreting anti-islet autoantibodies. Nature 300, 264–267 (1982). https://doi.org/10.1038/300264a0
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DOI: https://doi.org/10.1038/300264a0
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