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    • 4. 发明授权
    • Therapeutically useful molecules
    • 治疗有用的分子
    • US07951783B2
    • 2011-05-31
    • US10581773
    • 2004-12-06
    • Hans J. StaussLiquan GaoShao-An Xue
    • Hans J. StaussLiquan GaoShao-An Xue
    • A61K48/00
    • C07K14/7051A61K35/17C12N5/0636C12N7/00C12N15/86C12N2740/10043
    • A T cell receptor molecule (TCR) containing an alpha chain portion and a beta chain portion wherein the alpha chain portion contains three complementarity determining regions (CDRs): CDR1α: SSYSPS CDR2α: YTSAATL CDR3α: VVSPF-SGGGADGLT or comprising or consisting of SPFSGGGADGLT and the beta chain portion contains three complementarity determining regions (CDRs): CDR1β: DFQATT CDR2β: SNEGSKA CDR3β: comprising SARDGGEG or comprising or consisting of RDGGEGSETQY, or wherein up to three amino acid residues in one or more CDRs are replaced by another amino acid residue. The invention also includes polynucleotides encoding the TCR molecules, and host cells containing the said polynucleotides. Patient derived T cells may have the polynucleotides encoding the TCR molecules introduced therein, and the engineered T cells may be introduced into the patient in order to combat a WT1-expressing malignancy.
    • 含有α链部分和β链部分的AT细胞受体分子(TCR),其中α链部分含有三个互补决定区(CDR):CDR1α:SSYSPSCDR2α:YTSAATLCDR3α:VVSPF-SGGGADGLT或由SPFSGGGADGLT和 β链部分包含三个互补决定区(CDR):CDR1和bgr::DFQATT CDR2&bgr;:SNEGSKA CDR3&bgr::包含SARDGGEG或包含或由RDGGEGSETQY组成,或其中一个或多个CDR中的多达三个氨基酸残基被另一个氨基 酸残渣。 本发明还包括编码TCR分子的多核苷酸和含有所述多核苷酸的宿主细胞。 患者衍生的T细胞可以具有编码其中引入的TCR分子的多核苷酸,并且可以将经工程化的T细胞引入患者体内,以抵抗表达WT1的恶性肿瘤。
    • 5. 发明申请
    • Therapeutically useful molecules
    • 治疗有用的分子
    • US20070191496A1
    • 2007-08-16
    • US10581773
    • 2004-12-06
    • Hans StaussLiquan GaoShao-An Xue
    • Hans StaussLiquan GaoShao-An Xue
    • C11D3/48
    • C07K14/7051A61K35/17C12N5/0636C12N7/00C12N15/86C12N2740/10043
    • A T cell receptor molecule (TCR) containing an alpha chain portion and a beta chain portion wherein the alpha chain portion contains three complementarity determining regions (CDRs): CDR1α: SSYSPS CDR2α: YTSAATL CDR3α: VVSPF-SGGGADGLT or comprising or consisting of SPFSGGGADGLT and the beta chain portion contains three complementarity determining regions (CDRs): CDR1β: DFQATT CDR2β: SNEGSKA CDR3β: comprising SARDGGEG or comprising or consisting of RDGGEGSETQY, or wherein up to three amino acid residues in one or more CDRs are replaced by another amino acid residue. The invention also includes polynucleotides encoding the TCR molecules, and host cells containing the said polynucleotides. Patient derived T cells may have the polynucleotides encoding the TCR molecules introduced therein, and the engineered T cells may be introduced into the patient in order to combat a WT1-expressing malignancy.
    • 含有α链部分和β链部分的AT细胞受体分子(TCR),其中α链部分含有三个互补决定区(CDR):CDR1alpha:SSYSPS CDR2alpha:YTSAATL CDR3alpha:VVSPF-SGGGADGLT或包含或由SPFSGGGADGLT组成, β链部分包含三个互补决定区(CDR):CDR1beta:DFQATT CDR2beta:SNEGSKA CDR3beta:包含SARDGGEG或包含或由RDGGEGSETQY组成,或其中一个或多个CDR中的多达三个氨基酸残基被另一个氨基酸残基替代。 本发明还包括编码TCR分子的多核苷酸和含有所述多核苷酸的宿主细胞。 患者衍生的T细胞可以具有编码其中引入的TCR分子的多核苷酸,并且可以将经工程化的T细胞引入患者体内,以抵抗表达WT1的恶性肿瘤。