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      Generation, affinity maturation, and characterization of a human anti-human NKG2D monoclonal antibody with dual antagonistic and agonistic activity.

      Journal of Molecular Biology

      Amino Acid Sequence, Antibodies, Immobilized, Antibodies, Monoclonal, biosynthesis, immunology, Antibody Affinity, Antibody Specificity, Cell Death, Cell Degranulation, Cell Line, Enzyme-Linked Immunosorbent Assay, Genetic Vectors, Humans, Immunoglobulin Fab Fragments, chemistry, Immunoglobulin G, Immunoglobulin Variable Region, Killer Cells, Natural, cytology, Surface Plasmon Resonance, physiology, Ligands, Molecular Sequence Data, NK Cell Lectin-Like Receptor Subfamily K, Peptide Library, Protein Structure, Tertiary, Sequence Alignment

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          Abstract

          In humans, NKG2D is an activating receptor on natural killer (NK) cells and a costimulatory receptor on certain T cells and plays a central role in mediating immune responses in autoimmune diseases, infectious diseases, and cancer. Monoclonal antibodies that antagonize or agonize immune responses mediated by human NKG2D are considered to be of broad and potent therapeutic utility. Nonetheless, monoclonal antibodies to NKG2D that are suitable for clinical investigations have not been published yet. Here, we describe the generation, affinity maturation, and characterization of a fully human monoclonal antibody to human NKG2D. Using phage display technology based on a newly generated naïve human Fab library in phage display vector pC3C followed by a tandem chain shuffling process designed for minimal deviation from natural human antibody sequences, we selected a human Fab, designated KYK-2.0, with high specificity and affinity to human NKG2D. KYK-2.0 Fab blocked the binding of the natural human NKG2D ligands MICA, MICB, and ULBP2 as potently as a commercially available mouse anti-human NKG2D monoclonal antibody in immunoglobulin G (IgG) format. Conversion of KYK-2.0 Fab to IgG1 resulted in subnanomolar avidity for human NKG2D. KYK-2.0 IgG1 was found to selectively recognize defined subpopulations of human lymphocytes known to express NKG2D, that is, the majority of human CD8+, CD16+, and CD56+ cells as well as a small fraction of human CD4+ cells. In solution, KYK-2.0 IgG1 interfered with the cytolytic activity of ex vivo expanded human NK cells. By contrast, immobilized KYK-2.0 IgG1 was found to strongly induce human NK cell activation. The dual antagonistic and agonistic activity promises a wide range of therapeutic applications for KYK-2.0 IgG1 and its derivatives.

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          Author and article information

          Journal
          18809410
          2659651
          10.1016/j.jmb.2008.09.008

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