AI Article Synopsis

  • A new humanized single chain antibody, named humMR1, has been developed to specifically target the EGFRvIII receptor, which is commonly found in various human cancers.
  • The humMR1 antibody was created by modifying the CDR loops of a murine antibody (MR1) to fit human frameworks, and it includes mutations to prevent interaction with the regular EGFR.
  • Tests, including MTT assays and ELISA, showed that humMR1 is highly specific for EGFRvIII and can inhibit the growth of cells overexpressing this receptor by 78.5%.

Article Abstract

Production of an efficient humanized single chain antibody is reported here to specifically target EGFRvIII, a truncated receptor expressed in a wide variety of human cancers. CDR loops of MR1, a phage display-derived murine single chain antibody developed against this mutant receptor, were grafted on human frameworks that had been selected based on similarity to MR1 in terms of two distinct parameters, variable domain protein sequence and CDR canonical structures. Moreover, two point mutations were introduced in CDR-H2 and CDR-H3 loops of the humanized antibody to destroy its cross-reactivity to wild-type EGFR. The resultant antibody, referred to as humMR1, was found by MTT assay, ELISA and western blot techniques to be highly specific for EGFRvIII. The affinity of this antibody for EGFRvIII-specific 14-amino acid synthetic peptide and HC2 cells were measured to be 1.87 × 10(10) and 2.17 × 10(10)/M respectively. This humanized antibody leads to 78.5% inhibition in proliferation of EGFRvIII-overexpressing cells.

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Source
http://dx.doi.org/10.1016/j.intimp.2013.12.006DOI Listing

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