| Literature DB >> 7542600 |
M A Poul1, M Cerutti, H Chaabihi, M Ticchioni, F X Deramoudt, A Bernard, G Devauchelle, M Kaczorek, M P Lefranc.
Abstract
Plasmid cassette-transfer vectors pBHuC chi and pBHuC gamma l have been designed which enable the construction of recombinant baculoviruses directing the co-expression of complete immunoglobulin in insect cells. We describe the application of these vectors for the expression of a human/mouse chimeric monoclonal antibody of potential immunosuppressive clinical value derived from a mouse anti-human CD29 monoclonal antibody (Mu-K20). The chimeric K20 light and heavy chains produced in sf9 insect cells were correctly processed and assembled into a normal immunoglobulin which is secreted into the culture medium of infected cells. The chimeric mAb Ch-K20-sf9 reproduces in vitro the functional properties of the parental mouse K20, including affinity and inhibition of lymphocyte proliferation. These results demonstrate that the baculovirus/insect cell expression system is suitable for the expression of fully active monoclonal antibodies of therapeutic value. Our generic cassette approach makes this system a very flexible and convenient one for the rapid production of either chimeric, humanized or human mAb with heavy and light chains of any isotype.Entities:
Mesh:
Substances:
Year: 1995 PMID: 7542600 DOI: 10.1002/eji.1830250731
Source DB: PubMed Journal: Eur J Immunol ISSN: 0014-2980 Impact factor: 5.532