| Literature DB >> 15105446 |
Ludger Grosse-Hovest1, Sigrid Müller, Rosa Minoia, Eckhard Wolf, Valeri Zakhartchenko, Hendrik Wenigerkind, Caroline Lassnig, Urban Besenfelder, Mathias Müller, Simon D Lytton, Gundram Jung, Gottfried Brem.
Abstract
Complex recombinant antibody fragments for modulation of immune function such as tumor cell destruction have emerged at a rapid pace and diverse anticancer strategies are being developed to benefit patients. Despite improvements in molecule design and expression systems, the quantity and stability, e.g., of single-chain antibodies produced in cell culture, is often insufficient for treatment of human disease, and the costs of scale-up, labor, and fermentation facilities are prohibitive. The ability to yield mg/ml levels of recombinant antibodies and the scale-up flexibility make transgenic production in plants and livestock an attractive alternative to mammalian cell culture as a source of large quantities of biotherapeutics. Here, we report on the efficient production of a bispecific single-chain antibody in the serum of transgenic rabbits and a herd of nine cloned, transgenic cattle. The bispecific protein, designated r28M, is directed to a melanoma-associated proteoglycan and the human CD28 molecule on T cells. Purified from the serum of transgenic animals, the protein is stable and fully active in mediating target cell-restricted T cell stimulation and tumor cell killing.Entities:
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Year: 2004 PMID: 15105446 PMCID: PMC406432 DOI: 10.1073/pnas.0308487101
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205