METHOD OF PREDICTING RESPONSIVENESS OF B CELL LINEAGE MALIGNANCIES TO ACTIVE IMMUNOTHERAPY
    1.
    发明申请
    METHOD OF PREDICTING RESPONSIVENESS OF B CELL LINEAGE MALIGNANCIES TO ACTIVE IMMUNOTHERAPY 审中-公开
    将B细胞系恶性疾病的反应性预测为活性免疫球蛋白的方法

    公开(公告)号:WO2012096975A3

    公开(公告)日:2014-04-24

    申请号:PCT/US2012020802

    申请日:2012-01-10

    Abstract: Predictive biomarkers identify those patients suffering from immunoglobulin positive (lg+) B lineage malignancies that are responsive to active immunotherapy, where the active immunotherapy comprises vaccination with a tumor-specific idiotype-immunogen. It is shown herein that patient responsiveness to the idiotype-immunogen is dependent upon the sequence of the immunogen, where an immunogen having a low number of tyrosine residues in the CDR1 (herein termed CDR1 -Y10) regions of one or both of the immunogen heavy and light chains is predictive of a positive anti-tumor response, while a high number of CDR1 tyrosine residues (herein termed CDR1 -Yhi) is predictive of a low anti tumor response.

    Abstract translation: 预测性生物标志物识别患有对主动免疫治疗有反应的免疫球蛋白阳性(IgG)B系恶性肿瘤的患者,其中主动免疫治疗包括用肿瘤特异性独特型免疫原接种疫苗。 这里显示了患者对独特型免疫原的反应性取决于免疫原的序列,其中免疫原重量的一个或两个的CDR1(这里称为CDR1-Y10)区域中具有低数量酪氨酸残基的免疫原 轻链可预测阳性的抗肿瘤反应,而大量的CDR1酪氨酸残基(这里称为CDR1-Yhi)预示着低的抗肿瘤反应。

    METHOD OF PREDICTING RESPONSIVENESS OF B CELL LINEAGE MALIGNANCIES TO ACTIVE IMMUNOTHERAPY
    9.
    发明申请
    METHOD OF PREDICTING RESPONSIVENESS OF B CELL LINEAGE MALIGNANCIES TO ACTIVE IMMUNOTHERAPY 审中-公开
    将B细胞系恶性疾病的反应性预测为活性免疫球蛋白的方法

    公开(公告)号:WO2012096975A2

    公开(公告)日:2012-07-19

    申请号:PCT/US2012/020802

    申请日:2012-01-10

    Abstract: Predictive biomarkers identify those patients suffering from immunoglobulin positive (lg + ) B lineage malignancies that are responsive to active immunotherapy, where the active immunotherapy comprises vaccination with a tumor-specific idiotype-immunogen. It is shown herein that patient responsiveness to the idiotype-immunogen is dependent upon the sequence of the immunogen, where an immunogen having a low number of tyrosine residues in the CDR1 (herein termed CDR1 -Y 10 ) regions of one or both of the immunogen heavy and light chains is predictive of a positive anti-tumor response, while a high number of CDR1 tyrosine residues (herein termed CDR1 -Y hi ) is predictive of a low anti tumor response.

    Abstract translation: 预测性生物标志物识别患有对主动免疫治疗有反应的免疫球蛋白阳性(IgG)B系恶性肿瘤的患者,其中主动免疫治疗包括用肿瘤特异性独特型免疫原接种疫苗。 这里显示了患者对独特型免疫原的反应性取决于免疫原的序列,其中免疫原重量的一个或两个的CDR1(这里称为CDR1-Y10)区域中具有低数量酪氨酸残基的免疫原 轻链可预测阳性的抗肿瘤反应,而大量的CDR1酪氨酸残基(这里称为CDR1-Yhi)预示着低的抗肿瘤反应。

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