Using a multistep polymerase chain reaction method, we have produced a construct in which a cDNA sequence encoding the extracellular domain of the human 55-kD tumor necrosis factor (TNF) receptor is attached to a sequence encoding the Fc portion and hinge region of a mouse IgG1 heavy chain through an oligomer encoding a thrombin-sensitive peptide linker. This construct was placed downstream from a cytomegalovirus promoter sequence, and expressed in Chinese hamster ovary cells. A secreted protein, capable of binding TNF and inactivating it, was produced by the transfected cells. Molecular characterization revealed that this soluble version of the TNF receptor was dimeric. Moreover, the protein could be quantitatively cleaved by treatment with thrombin. However, the monovalent extracellular domain prepared in this way has a greatly reduced TNF inhibitory activity compared with that of the bivalent inhibitor. Perhaps because of its high affinity for TNF, the chimeric protein is far more effective as a TNF inhibitor than are neutralizing monoclonal antibodies. This molecule may prove very useful as a reagent for the antagonism and assay of TNF and lymphotoxin from diverse species in health and disease, and as a means of deciphering the exact mechanism through which TNF interacts with the 55-kD receptor.
Article|
December 01 1991
A tumor necrosis factor (TNF) receptor-IgG heavy chain chimeric protein as a bivalent antagonist of TNF activity.
K Peppel,
K Peppel
Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, Texas 75235.
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D Crawford,
D Crawford
Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, Texas 75235.
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B Beutler
B Beutler
Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, Texas 75235.
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K Peppel
Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, Texas 75235.
D Crawford
Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, Texas 75235.
B Beutler
Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, Texas 75235.
Online ISSN: 1540-9538
Print ISSN: 0022-1007
J Exp Med (1991) 174 (6): 1483–1489.
Citation
K Peppel, D Crawford, B Beutler; A tumor necrosis factor (TNF) receptor-IgG heavy chain chimeric protein as a bivalent antagonist of TNF activity.. J Exp Med 1 December 1991; 174 (6): 1483–1489. doi: https://doi.org/10.1084/jem.174.6.1483
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