首页> 外国专利> MULTIMERIC COMPLEXES WITH IMPROVED IN VIVO STABILITY, PHARMACOKINETICS AND EFFICACY

MULTIMERIC COMPLEXES WITH IMPROVED IN VIVO STABILITY, PHARMACOKINETICS AND EFFICACY

机译:体内,稳定性,药代动力学和功效得到改善的多元复合物

摘要

The present invention concerns multimeric complexes based on antibody fusion proteins comprising an AD moiety attached to the C-terminal end of each antibody light chain. The complexes further comprise effector moities attached to DDD moieties. Two copies of the DDD moiety form a dimer that binds to the AD moiety. The complexes may be trimers, pentamers, hexamers or other multimers. The effector moieties may be selected from a second antibody or antigen-binding fragment thereof, a cytokine, an interferon, a toxin, an antigen, a xenoantigen, a hapten, a protamine, a hormone, an enzyme, a ligand-binding protein, a pro-apoptotic agent and an anti-angiogenic agent. Surprisingly, attachment of the AD moiety to the C-terminal end of the antibody light chain results in improved pharmacokinetics and in vivo stability and efficacy, compared to homologous complexes wherein the AD moiety is attached to the antibody heavy chain.
机译:本发明涉及基于抗体融合蛋白的多聚体复合物,所述抗体融合蛋白包含附着于每个抗体轻链的C末端的AD部分。所述复合物还包含与DDD部分连接的效应子部分。 DDD部分的两个副本形成与AD部分结合的二聚体。络合物可以是三聚体,五聚体,六聚体或其他多聚体。效应物部分可以选自第二抗体或其抗原结合片段,细胞因子,干扰素,毒素,抗原,异种抗原,半抗原,鱼精蛋白,激素,酶,配体结合蛋白,促凋亡剂和抗血管生成剂。令人惊讶地,与其中AD部分连接至抗体重链的同源复合物相比,AD部分连接至抗体轻链的C末端导致改善的药代动力学以及体内稳定性和功效。

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