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Therapeutic antigen binding molecules having FcRn binding domains that promote antigen clearance

机译:具有促进抗原清除的FcRn结合域的治疗性抗原结合分子

摘要

The present invention provides: a modified FcRn-binding domain having an enhanced affinity for the Fc Receptor neonatal (FcRn) at neutral pH; an antigen-binding molecule comprising said FcRn-binding domain, which has low immunogenicity, high stability and form only a few aggregates; a modified antigen-binding molecule having an increased FcRn-binding activity at neutral or acidic pH without an increased binding activity at neutral pH for a pre-existing anti-drug antibody; use of the antigen-binding molecules for improving antigen-binding molecule-mediated antigen uptake into cells; use of the antigen-binding molecules for reducing the plasma concentration of a specific antigen; use of the modified FcRn-binding domain for increasing the total number of antigens to which a single antigen-binding molecule can bind before its degradation; use of the modified FcRn-binding domain for improving pharmacokinetics of an antigen-binding molecule; methods for decreasing the binding activity for a pre-existing anti-drug antibody; and methods for producing said antigen-binding molecules.
机译:本发明提供:在中性pH下对Fc受体新生儿(FcRn)具有增强的亲和力的修饰的FcRn结合结构域;包含所述FcRn结合结构域的抗原结合分子,其免疫原性低,稳定性高并且仅形成少数聚集体;一种修饰的抗原结合分子,其在中性或酸性pH下具有增加的FcRn结合活性,而在中性pH下对已有的抗药物抗体没有增加的结合活性;抗原结合分子用于改善抗原结合分子介导的抗原摄取到细胞中的用途;抗原结合分子用于降低特定抗原的血浆浓度的用途;修饰的FcRn结合结构域用于增加单个抗原结合分子在其降解之前可以结合的抗原总数的用途;修饰的FcRn结合结构域用于改善抗原结合分子的药代动力学的用途;降低预先存在的抗药物抗体结合活性的方法;和产生所述抗原结合分子的方法。

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