首页> 外国专利> Multiple signaling pathways induced by hexavalent, monospecific and bispecific antibodies for enhanced toxicity to B-cell lymphomas and other diseases

Multiple signaling pathways induced by hexavalent, monospecific and bispecific antibodies for enhanced toxicity to B-cell lymphomas and other diseases

机译:六价,单特异性和双特异性抗体诱导的多种信号通路,可增强对B细胞淋巴瘤和其他疾病的毒性

摘要

Disclosed herein are compositions and methods of use comprising hexavalent DNL complexes. Preferably, the complexes comprise anti-CD20 and/or anti-CD22 antibodies or fragments thereof. More preferably, the anti-CD20 antibody is veltuzumab and the anti-CD22 antibody is epratuzumab. Administration of the subject hexavalent DNL complexes induces apoptosis and cell death of target cells in diseases such as B-cell lymphomas or leukemias, autoimmune disease or immune dysfunction disease. In most preferred embodiments, the DNL complexes increase levels of phosphorylated p38 and PTEN, decrease levels of phosphorylated Lyn, Akt, ERK, IKKα/β and IκBα, increase expression of RKIP and Bax and decrease expression of Mcl-1, Bcl-xL, Bcl-2, and phospho-BAD in target cells. The subject DNL complexes show EC50 values for inhibiting tumor cell growth in the low nanomolar or even sub-nanomolar concentration range.
机译:本文公开了包含六价DNL复合物的组合物和使用方法。优选地,复合物包含抗CD20和/或抗CD22抗体或其片段。更优选地,抗CD20抗体是维妥珠单抗,抗CD22抗体是埃普珠单抗。在诸如B细胞淋巴瘤或白血病,自身免疫疾病或免疫功能障碍疾病之类的疾病中,施用主题六价DNL复合物可诱导靶细胞凋亡和细胞死亡。在最优选的实施方案中,DNL复合物增加磷酸化的p38和PTEN的水平,降低磷酸化的Lyn,Akt,ERK,IKKα/β和IκBα的水平,增加RKIP和Bax的表达并降低Mcl-1,Bcl-xL的表达, Bcl-2和磷酸BAD在靶细胞中。主题DNL配合物显示出在低纳摩尔浓度甚至亚纳摩尔浓度范围内抑制肿瘤细胞生长的EC 50 值。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号