Antigen-Specific Monoclonal Antibodies Isolated from B Cells Expressing Constitutively Active STAT5
Author(s) -
Ferenc A. Scheeren,
Caroline M. M. van Geelen,
Etsuko Yasuda,
Hergen Spits,
Tim Beaumont
Publication year - 2011
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0017189
Subject(s) - monoclonal antibody , antigen , biology , antibody , microbiology and biotechnology , stat protein , virology , signal transduction , immunology , stat3
Background Fully human monoclonal antibodies directed against specific pathogens have a high therapeutic potential, but are difficult to generate. Methodology/Principal Findings Memory B cells were immortalized by expressing an inducible active mutant of the transcription factor Signal Transducer and Activator of Transcription 5 (STAT5). Active STAT5 inhibits the differentiation of B cells while increasing their replicative life span. We obtained cloned B cell lines, which produced antibodies in the presence of interleukin 21 after turning off STAT5. We used this method to obtain monoclonal antibodies against the model antigen tetanus toxin. Conclusions/Significance Here we describe a novel and relatively simple method of immortalizing antigen-specific human B cells for isolation of human monoclonal antibodies. These results show that STAT5 overexpression can be employed to isolate antigen specific antibodies from human memory B cells.
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