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一种用于生物治疗药物免疫原性风险评估的实时成像方法,以量化树突状细胞内化情况。

A real-time imaging approach to quantify dendritic cell internalization for immunogenicity risk assessment of biotherapeutics.

作者信息

Yin Zhaojun, Tran Peter, Guerrero Joyce, Low Justin, Xie Qing, Peng Kun

机构信息

Department BioAnalytical Sciences, Genentech, Inc., South San Francisco, CA, United States.

出版信息

Front Immunol. 2025 Sep 12;16:1632302. doi: 10.3389/fimmu.2025.1632302. eCollection 2025.

Abstract

The presence of treatment-emergent anti-drug antibodies (ADAs) can pose challenges during biotherapeutic development by compromising drug safety and efficacy. Early assessment of immunogenicity risk is essential to mitigate these risks. Dendritic cells (DCs) are crucial for priming CD4 T cells and necessary for effective antibody production. Therefore, DC internalization has been investigated as a predictive tool for evaluating the immunogenicity risk of biotherapeutics. Previously reported flow cytometry-based DC internalization assays, including our own, have faced several limitations. These limitations included low throughput due to a restricted DC supply from healthy donors, restriction to Fc-containing antibody-based biotherapeutics, and offering only endpoint data. To address these limitations, we explored both direct and indirect labeling approaches using the IncuCyte® real-time imaging platform. Our findings revealed that indirect labeling approach with the commonly used Fab anti-Fc reagents was unsuitable for DC internalization assays due to significant assay background noises and assay bias when evaluating biotherapeutics of different frameworks. In contrast, using direct labeling with Biotracker Orange demonstrated improved predictability, required fewer DCs, and was suitable for high-throughput screening. Additionally, this approach facilitates constant monitoring of the internalization process, offering a comprehensive understanding of cell morphology changes and internalization kinetics. Using a panel of 25 test therapeutic antibodies with known clinical ADA results, the IncuCyte®-based direct labeling assay demonstrated significant improvements in predicting the immunogenicity risk of the tested molecules. The assay demonstrated a high correlation between internalization and clinical immunogenicity risk, outperforming our previous flow cytometry-based results. Overall, the IncuCyte®-based direct labeling assay using Biotracker Orange represents a significant advancement compared to our previous flow cytometry assay. This new technique is a valuable addition to our immunogenicity risk assessment toolbox, and will ultimately lead to more informed decision-making in the early development of biotherapeutics.

摘要

治疗中出现的抗药物抗体(ADA)的存在可能会在生物治疗药物开发过程中对药物安全性和疗效产生影响,从而带来挑战。对免疫原性风险进行早期评估对于降低这些风险至关重要。树突状细胞(DC)对于启动CD4 T细胞至关重要,是有效产生抗体所必需的。因此,DC内化已被研究作为评估生物治疗药物免疫原性风险的一种预测工具。先前报道的基于流式细胞术的DC内化检测方法,包括我们自己的方法,都面临一些局限性。这些局限性包括由于健康供体的DC供应受限导致通量低、仅限于基于含Fc抗体的生物治疗药物以及仅提供终点数据。为了解决这些局限性,我们使用IncuCyte®实时成像平台探索了直接和间接标记方法。我们的研究结果表明,使用常用的Fab抗Fc试剂的间接标记方法不适用于DC内化检测,因为在评估不同框架的生物治疗药物时存在显著的检测背景噪声和检测偏差。相比之下,使用Biotracker Orange进行直接标记显示出更好的可预测性,所需的DC数量更少,并且适用于高通量筛选。此外,这种方法有助于对内化过程进行持续监测,从而全面了解细胞形态变化和内化动力学。使用一组25种具有已知临床ADA结果的测试治疗性抗体,基于IncuCyte®的直接标记检测在预测测试分子的免疫原性风险方面有显著改进。该检测显示内化与临床免疫原性风险之间具有高度相关性,优于我们之前基于流式细胞术的结果。总体而言,与我们之前的流式细胞术检测相比,使用Biotracker Orange的基于IncuCyte®的直接标记检测是一个重大进步。这项新技术是我们免疫原性风险评估工具箱中的一项有价值的补充,并最终将在生物治疗药物的早期开发中带来更明智的决策。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ca3/12463596/513224b74e21/fimmu-16-1632302-g001.jpg

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