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Article type: Research Article
Authors: Steenbakkers, Peter G. A.a; | Van Wezenbeek, Peter M.G.F.a | van Zanten, Jacobab | Thet, T. Hauwb
Affiliations: [a] Department of Immunology, Organon International b.v., Oss, The Netherlands | [b] Department of Clinical Immunology, University Hospital, Groningen, The Netherlands
Note: [] Address reprint requests to Dr. Peter G. A. Steenbakkers, Department of Immunology, Organon International, P.O.B. 20, 5340 BH Oss, The Netherlands.
Abstract: Human anti-cytomegalovirus (CMV) specific B cells were enriched to a purity of up to 38% on CMV-coated dishes and subsequently clonally expanded in the presence of human T cell supernatant and irradiated murine thymoma helper cells. The expanded cells were immortalized by a mini-electrofusion with K6H6B5 myeloma cells. Twenty-two anti-CMV positive B cell clones could be obtained from as little as 1.5 ml donor blood. The majority of these clones produced anti-CMV antibodies of the 19G class. Ten anti-CMV positive B cell clones were submitted to separate mini-electrofusions yielding stable, human anti-CMV IgG-producing hybridomas in six out of ten fusions. These antibodies recognized different proteins of the CMV virus, as deduced from the immunofluorescence staining pattern on infected human fibroblasts.
Keywords: selection, antigen-specific B cells, human monoclonal antibody, CMV B cell clone, mini-electrofusion
DOI: 10.3233/HAB-1993-4402
Journal: Human Antibodies, vol. 4, no. 4, pp. 166-173, 1993
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