The potential of hybrid antibodies secreted by hybrid-hybridomas in tumour therapy.

Using a simple method for the selection of hybrid cell growth from the cell fusion of pairs of existing hybridoma cell lines, 2 different hybrid-hybridoma cell lines were produced. Both hybrid-hybridomas secreted bi-specific antibody with similar specificity for human CD3 and for mouse Thy-l but in...

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Principais autores: Clark, M, Gilliland, L, Waldmann, H
Formato: Journal article
Idioma:English
Publicado em: 1988
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author Clark, M
Gilliland, L
Waldmann, H
author_facet Clark, M
Gilliland, L
Waldmann, H
author_sort Clark, M
collection OXFORD
description Using a simple method for the selection of hybrid cell growth from the cell fusion of pairs of existing hybridoma cell lines, 2 different hybrid-hybridoma cell lines were produced. Both hybrid-hybridomas secreted bi-specific antibody with similar specificity for human CD3 and for mouse Thy-l but in one case the parental antibody isotypes were both IgG2b and in the other case the CD3 antibody was IgG2b and the anti-Thy-l antibody was IgG2c. In a model in vitro system both bi-specific antibodies were able to elicit potent cell killing of a Thy-l expressing mouse tumour cell line by human effector cell blasts. The cell blasts were generated from resting peripheral blood mononuclear cells using a mitogenic monoclonal antibody (MAb) (YTH361). The parental anti-Thy-l IgG2b but not the IgG2c antibody was also able to mediate cell killing by ADCC. This ADCC killing was inhibited by a MAb to the CD16 Fc receptor but the killing elicited by the bi-specific antibodies was not. Both mechanisms of tumour cell killing may be of great potential in human tumour therapy with MAbs.
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spelling oxford-uuid:fd51337a-a9be-4b92-a55c-4540e43296922022-03-27T13:27:59ZThe potential of hybrid antibodies secreted by hybrid-hybridomas in tumour therapy.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:fd51337a-a9be-4b92-a55c-4540e4329692EnglishSymplectic Elements at Oxford1988Clark, MGilliland, LWaldmann, HUsing a simple method for the selection of hybrid cell growth from the cell fusion of pairs of existing hybridoma cell lines, 2 different hybrid-hybridoma cell lines were produced. Both hybrid-hybridomas secreted bi-specific antibody with similar specificity for human CD3 and for mouse Thy-l but in one case the parental antibody isotypes were both IgG2b and in the other case the CD3 antibody was IgG2b and the anti-Thy-l antibody was IgG2c. In a model in vitro system both bi-specific antibodies were able to elicit potent cell killing of a Thy-l expressing mouse tumour cell line by human effector cell blasts. The cell blasts were generated from resting peripheral blood mononuclear cells using a mitogenic monoclonal antibody (MAb) (YTH361). The parental anti-Thy-l IgG2b but not the IgG2c antibody was also able to mediate cell killing by ADCC. This ADCC killing was inhibited by a MAb to the CD16 Fc receptor but the killing elicited by the bi-specific antibodies was not. Both mechanisms of tumour cell killing may be of great potential in human tumour therapy with MAbs.
spellingShingle Clark, M
Gilliland, L
Waldmann, H
The potential of hybrid antibodies secreted by hybrid-hybridomas in tumour therapy.
title The potential of hybrid antibodies secreted by hybrid-hybridomas in tumour therapy.
title_full The potential of hybrid antibodies secreted by hybrid-hybridomas in tumour therapy.
title_fullStr The potential of hybrid antibodies secreted by hybrid-hybridomas in tumour therapy.
title_full_unstemmed The potential of hybrid antibodies secreted by hybrid-hybridomas in tumour therapy.
title_short The potential of hybrid antibodies secreted by hybrid-hybridomas in tumour therapy.
title_sort potential of hybrid antibodies secreted by hybrid hybridomas in tumour therapy
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