Université de Paris-Saclay, CEA, INRAE, Département Médicaments et Technologies pour la Santé, SIMoS, Gif-sur-Yvette, France.
Deeptope SAS, Orsay, France.
Front Immunol. 2023 Jul 28;14:1197919. doi: 10.3389/fimmu.2023.1197919. eCollection 2023.
Removal of CD4 T cell epitopes from therapeutic antibody sequences is expected to mitigate their potential immunogenicity, but its application is complicated by the location of their T cell epitopes, which mainly overlap with complementarity-determining regions. We therefore evaluated the flexibility of antibody sequences to reduce the predicted affinity of corresponding peptides for HLA II molecules and to maintain antibody binding to its target in order to guide antibody engineering for mitigation of predicted immunogenicity. Permissive substitutions to reduce affinity of peptides for HLA II molecules were identified by establishing a heatmap of HLA class II binding using T-cell epitope prediction tools, while permissive substitutions preserving binding to the target were identified by means of deep mutational scanning and yeast surface display. Combinatorial libraries were then designed to identify active clones. Applied to adalimumab, an anti-TNFα human antibody, this approach identified 200 mutants with a lower HLA binding score than adalimumab. Three mutants were produced as full-length antibodies and showed a higher affinity for TNFα and neutralization ability than adalimumab. This study also sheds light on the permissiveness of antibody sequences with regard to functionality and predicted T cell epitope content.
从治疗性抗体序列中去除 CD4 T 细胞表位有望减轻其潜在的免疫原性,但由于 T 细胞表位的位置主要与互补决定区重叠,其应用变得复杂。因此,我们评估了抗体序列的灵活性,以降低相应肽段与 HLA II 分子的预测亲和力,并保持抗体与其靶标的结合,从而指导抗体工程以减轻预测的免疫原性。通过使用 T 细胞表位预测工具建立 HLA Ⅱ类结合的热图,确定了降低肽段与 HLA II 分子亲和力的允许取代,而通过深度突变扫描和酵母表面展示确定了保留与靶标结合的允许取代。然后设计组合文库以鉴定活性克隆。将该方法应用于抗 TNFα 人源抗体阿达木单抗,鉴定出 200 个 HLA 结合评分低于阿达木单抗的突变体。生成了三个全长抗体突变体,与阿达木单抗相比,它们对 TNFα 的亲和力更高,中和能力更强。这项研究还揭示了抗体序列在功能和预测的 T 细胞表位含量方面的允许性。