FIELD: biotechnology.
SUBSTANCE: invention relates to a method for producing a therapeutic agent for humans involving immunization of a genetically modified mouse with an antigen of interest. At the same time, the specified mouse contains the following in the endogenous TCR locus α: replacement of endogenous TCR V segment α at least one rearranged TCR V segmentα human, and replacement of the endogenous segment of TCR Jα at least one unrearranged human TCR segment Jα, and/or the following in the endogenous TCRβ locus: replacement of an endogenous TCR Vβ segment with at least one unrearranged human TCR Vβ segment, replacement of an endogenous TCR Dβ segment with at least one unrearranged human TCR Dβ segment, and replacement of an endogenous TCR Jβ segment with at least one unrearranged human TCR Jβ segment.
EFFECT: invention is effective for obtaining a therapeutic agent for humans containing a TCR variable domain.
18 cl, 19 dwg, 4 tbl, 10 ex
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Authors
Dates
2023-06-01—Published
2012-10-26—Filed