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Rapid selection of cell subpopulation-specific human monoclonal antibodies from a synthetic phage antibody library.
Author(s) -
John de Kruif,
Leon W.M.M. Terstappen,
Edwin Boel,
Ton Logtenberg
Publication year - 1995
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.92.9.3938
Subject(s) - phage display , antibody , monoclonal antibody , biology , microbiology and biotechnology , flow cytometry , antigen , peptide library , population , immunoglobulin light chain , epitope , virology , immunology , gene , peptide sequence , genetics , demography , sociology
Peripheral blood leukocytes incubated with a semisynthetic phage antibody library and fluorochrome-labeled CD3 and CD20 antibodies were used to isolate human single-chain Fv antibodies specific for subsets of blood leukocytes by flow cytometry. Isolated phage antibodies showed exclusive binding to the subpopulation used for selection or displayed additional binding to a restricted population of other cells in the mixture. At least two phage antibodies appeared to display hitherto-unknown staining patterns of B-lineage cells. This approach provides a subtractive procedure to rapidly obtain human antibodies against known and novel surface antigens in their native configuration, expressed on phenotypically defined subpopulations of cells. This approach does not depend on immunization procedures or the necessity to repeatedly construct phage antibody libraries.

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