Cloned transgenic farm animals produce a bispecific antibody for T cell-mediated tumor cell killing.

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.

[1]  M. Little,et al.  Effect of domain order on the activity of bacterially produced bispecific single-chain Fv antibodies. , 2003, Journal of molecular biology.

[2]  H. Rammensee,et al.  A recombinant bispecific single‐chain antibody induces targeted, supra‐agonistic CD28‐stimulation and tumor cell killing , 2003, European journal of immunology.

[3]  L. Houdebine Antibody manufacture in transgenic animals and comparisons with other systems , 2002, Current Opinion in Biotechnology.

[4]  B. Osborne,et al.  Cloned transchromosomic calves producing human immunoglobulin , 2002, Nature Biotechnology.

[5]  Alan Dove,et al.  Uncorking the biomanufacturing bottleneck , 2002, Nature Biotechnology.

[6]  Trisha Gura,et al.  Therapeutic antibodies: Magic bullets hit the target , 2002, Nature.

[7]  P. Christou,et al.  Plantibodies: applications, advantages and bottlenecks. , 2002, Current opinion in biotechnology.

[8]  J. Lakritz,et al.  Serum immunoglobulin G concentrations in calves fed fresh colostrum or a colostrum supplement. , 2002, Journal of veterinary internal medicine.

[9]  R. Wanke,et al.  Nuclear transfer in cattle with non‐transfected and transfected fetal or cloned transgenic fetal and postnatal fibroblasts , 2001, Molecular reproduction and development.

[10]  J. Larrick,et al.  Production of secretory IgA antibodies in plants. , 2001, Biomolecular engineering.

[11]  R. Clark Fibrin sealant in wound repair: a systematic survey of the literature , 2000, Expert opinion on investigational drugs.

[12]  A. Spriel,et al.  Immunotherapeutic perspective for bispecific antibodies. , 2000 .

[13]  M. Little,et al.  Of mice and men: hybridoma and recombinant antibodies. , 2000, Immunology today.

[14]  A. Schnieke,et al.  Production of gene-targeted sheep by nuclear transfer from cultured somatic cells , 2000, Nature.

[15]  B. Dörken,et al.  A recombinant bispecific single-chain antibody, CD19 x CD3, induces rapid and high lymphoma-directed cytotoxicity by unstimulated T lymphocytes. , 2000, Blood.

[16]  H. Meade,et al.  Transgenic milk as a method for the production of recombinant antibodies , 1999, Journal of Immunological Methods.

[17]  R. Merion Current use of polyclonal antilymphocyte antibody preparations. , 1999, Transplantation proceedings.

[18]  J. Castilla,et al.  Engineering passive immunity in transgenic mice secreting virus-neutralizing antibodies in milk , 1998, Nature Biotechnology.

[19]  I Wilmut,et al.  Human factor IX transgenic sheep produced by transfer of nuclei from transfected fetal fibroblasts. , 1997, Science.

[20]  I. Wilmut,et al.  "Viable Offspring Derived from Fetal and Adult Mammalian Cells" (1997), by Ian Wilmut et al. , 2014 .

[21]  I. Wilmut,et al.  Sheep cloned by nuclear transfer from a cultured cell line , 1996, Nature.

[22]  T. Lehner,et al.  Generation and assembly of secretory antibodies in plants , 1995, Science.

[23]  D. Segal,et al.  Retargeting of CTL by an efficiently refolded bispecific single-chain Fv dimer produced in bacteria. , 1995, Journal of immunology.

[24]  J. Kass,et al.  Regulatory regions 3' of the immunoglobulin heavy chain intronic enhancer differentially affect expression of a heavy chain transgene in resting and activated B cells. , 1995, Journal of immunology.

[25]  D. Kranz,et al.  Efficient tumor cell lysis mediated by a bispecific single chain antibody expressed in Escherichia coli. , 1994, Journal of immunology.

[26]  E. Voss,et al.  Construction, expression, and activity of a bivalent bispecific single-chain antibody. , 1994, The Journal of biological chemistry.

[27]  G. Brem,et al.  Laparoscopic embryo transfer in rabbits. , 1993, Journal of reproduction and fertility.

[28]  H. Gram,et al.  High‐level expression of a human immunoglobulin γ1 transgene depends on switch region sequences , 1992, European journal of immunology.

[29]  R. Palmiter,et al.  Expression of mouse IgA by transgenic mice, pigs and sheep , 1991, European journal of immunology.

[30]  H. Lenz,et al.  Genes encoding a mouse monoclonal antibody are expressed in transgenic mice, rabbits and pigs. , 1991, Gene.

[31]  L. Björck,et al.  Protein L: an immunoglobulin light chain-binding bacterial protein. Characterization of binding and physicochemical properties. , 1989, The Journal of biological chemistry.

[32]  E. Winnacker,et al.  Production of transgenic mice, rabbits and pigs by microinjection into pronuclei , 1985 .

[33]  J. Ledbetter,et al.  Antibodies to Tp67 and Tp44 augment and sustain proliferative responses of activated T cells. , 1985, Journal of immunology.

[34]  R. Palmiter,et al.  Production of transgenic rabbits, sheep and pigs by microinjection , 1985, Nature.

[35]  R. Reisfeld,et al.  Monoclonal antibody-directed effector cells selectively lyse human melanoma cells in vitro and in vivo. , 1983, Proceedings of the National Academy of Sciences of the United States of America.