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NKp46 特异性单域抗体可方便地工程化为各种有效的 NK 细胞衔接器形式。

NKp46-specific single domain antibodies enable facile engineering of various potent NK cell engager formats.

机构信息

Protein Engineering and Antibody Technologies, Merck Healthcare KGaA, Darmstadt, Germany.

Institute for Organic Chemistry and Biochemistry, Technical University of Darmstadt, Darmstadt, Germany.

出版信息

Protein Sci. 2023 Mar;32(3):e4593. doi: 10.1002/pro.4593.

Abstract

Herein, we describe the generation of potent NK cell engagers (NKCEs) based on single domain antibodies (sdAbs) specific for NKp46 harboring the humanized Fab version of Cetuximab for tumor targeting. After immunization of camelids, a plethora of different VHH domains were retrieved by yeast surface display. Upon reformatting into Fc effector-silenced NKCEs targeting NKp46 and EGFR in a strictly monovalent fashion, the resulting bispecific antibodies elicited potent NK cell-mediated killing of EGFR-overexpressing tumor cells with potencies (EC killing) in the picomolar range. This was further augmented via co-engagement of Fcγ receptor IIIa (FcγRIIIa). Importantly, NKp46-specific sdAbs enabled the construction of various NKCE formats with different geometries and valencies which displayed favorable biophysical and biochemical properties without further optimization. By this means, killing capacities were further improved significantly. Hence, NKp46-specific sdAbs are versatile building blocks for the construction of different NKCE formats.

摘要

在这里,我们描述了基于针对 NKp46 的单域抗体 (sdAb) 的强效自然杀伤细胞衔接器 (NKCE) 的产生,这些 sdAb 携带用于肿瘤靶向的人源化 Fab 版本的西妥昔单抗。在对骆驼进行免疫后,通过酵母表面展示回收了大量不同的 VHH 结构域。在重新构建成以严格单价方式靶向 NKp46 和 EGFR 的 Fc 效应沉默 NKCE 后,所得的双特异性抗体以皮摩尔级的效力(EC 杀伤)引发了过表达 EGFR 的肿瘤细胞的强烈 NK 细胞介导的杀伤。通过共结合 Fcγ 受体 IIIa (FcγRIIIa) 进一步增强了这种作用。重要的是,NKp46 特异性 sdAb 使具有不同几何形状和价态的各种 NKCE 形式的构建成为可能,这些形式具有有利的生物物理和生化特性,无需进一步优化。通过这种方式,杀伤能力得到了显著提高。因此,NKp46 特异性 sdAb 是构建不同 NKCE 形式的多功能构建块。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9f6/9951198/d38e83adaf97/PRO-32-e4593-g002.jpg

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