Literature DB >> 1289988

Human monoclonal IgM antibodies from foetal B-cell hybridomas directed against a surface antigen on human tumour cells.

J Bohn1, O Josimovic-Alasevic, U Settmacher, S T Kiessig, A Lukowsky, H D Volk, T Diamantstein, R Von Baehr, S Jahn.   

Abstract

In order to assess the existence of B lymphocytes capable of producing anti-tumour antibodies in non-tumour-bearing individuals, human lymphocytes derived from foetuses and adults were fused with the heteromyeloma cell line CB-F7. By indirect immunofluorescence, 29 out of 4,472 IgM-producing hybridomas (from 8 foetuses and 8 adults) were shown to produce antibodies which bind to colon carcinoma lines Colo205 and SW620, Raji lymphoma cells and small cell carcinoma of the lung. In vitro growth of tumour cells recognized by these antibodies was inhibited. The antibodies also mediated complement-dependent cytotoxicity. All antibodies tested recognized a cell surface molecule of 55 kDa. Southern blot hybridization analysis of hybridoma DNA with a human JH probe showed that the hybridomas were derived from clonally unrelated B cells. These results demonstrate that human foetal and adult B cells from non-tumour-bearing individuals are able to produce IgM antibodies recognizing defined cell surface molecules expressed on some tumour cells.

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Year:  1992        PMID: 1289988     DOI: 10.1016/0923-2494(92)80111-w

Source DB:  PubMed          Journal:  Res Immunol        ISSN: 0923-2494


  1 in total

1.  Tumour cell binding by a human monoclonal IgM antibody from the spleen of a non-tumour-associated patient is due to somatic mutations in the VH gene.

Authors:  J Bohn; B Niemann; D Roggenbuck; W Döcke; S Jahn
Journal:  Clin Exp Immunol       Date:  1995-03       Impact factor: 4.330

  1 in total

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