PO.CL05.01 · 临床研究

CAR检测试剂——引领CAR T分析技术的进步

CAR Detection Reagents - Pioneering advances in CAR T analytics

海报缩略图:CAR检测试剂——引领CAR T分析技术的进步
编号 3718 展板 20 时间 4/20 02:00–05:00 区域 Section 40 主讲 Stephan Wilmes, Dr Rer Nat
分会场 Adoptive Cell Therapy 1
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作者与单位 Authors & Affiliations

Stephan Wilmes, Desiré Missing, Anja Brauchle, Nadine Borgelt, Johanna Müllers, Monika Winkels, Larissa Möckel, Michaela Niemöller, Dagmar Häußler-Kuballa, Franziska Antonia Bertram, Olga Goldbach, Dominik Poschen, Astrid Imann, Silvia Rüberg, Anijutta Appelshoffer, Fabio El Yassouri, Marsilius Mues, Volker Nölle, Andreas Bosio, Christian Dose, Anne Richter

Miltenyi Biotec B.V. & Co. KG, Bergisch Gladbach, Germany

摘要 Abstract

中文摘要
嵌合抗原受体(CAR)T细胞疗法已经变革了癌症治疗,为血液系统B细胞恶性肿瘤(包括白血病、淋巴瘤和多发性骨髓瘤)患者提供了靶向且有效的治疗选择。其在靶向并清除癌细胞方面的精准性,使其成为细胞免疫治疗中一种有前景的方法。准确检测CAR的表达对于研究、临床前应用、临床生产及患者免疫监测至关重要。为满足这些需求,我们开发了针对CAR工程化T细胞和NK细胞流式细胞分析优化的CAR检测试剂,确保卓越的质量和特异性。我们基于重组抗原的CAR检测试剂模拟CAR与肿瘤细胞的相互作用,靶向关键的细胞表面抗原,如CD19、BCMA、CD22、MSLN、CD123、B7-H3、HER2和CD33。我们还制备了针对CD19 FMC63和GD2 14G2a CAR的抗CAR抗体,以及针对商业化CAR T细胞产品中常用的G4S接头和Whitlow接头的接头特异性抗体。所有这些试剂均采用经工程化改造的人IgG1 Fc区,以防止与Fcgamma受体结合,确保无背景分析。它们提供多种偶联物形式(如荧光染料、生物素),在panel设计中具有卓越的性能和灵活性。我们的流式细胞分析证实,在原代CAR T/NK细胞和模型细胞系上,染色明亮且特异、背景低,这对于产品生产和患者监测中可靠的CAR T细胞计数至关重要。CAR检测试剂也适用于磁激活细胞分选(MACS)。在过继细胞转移后的免疫监测中,从血液或PBMC中快速分离CAR T细胞可能至关重要,因为这些样本中的CAR T细胞数量可能极低,低于检测限。磁富集显著提高了分析灵敏度,确保对CAR T细胞持久性的长期监测,这对于评估治疗疗效和患者应答至关重要。此外,MACS纯化的CAR T细胞可以进行深度表型分析和功能测定。在组织样本中检测CAR T细胞对于了解其在体内的分布和活性至关重要。这一能力使研究人员和临床医生能够评估肿瘤部位的CAR T细胞浸润和治疗效果,为治疗有效性和耐药机制提供见解。利用荧光显微镜,我们展示了使用FMC63靶向抗CD19 CAR抗体,在经治疗小鼠的新鲜冷冻和PFA固定组织样本中对CD19 FMC63 CAR T细胞进行精确检测和计数。这一方法增进了我们对CAR T细胞体内动态的理解。总之,这些用途广泛的CAR检测试剂是推进CAR T细胞研究和临床治疗的宝贵工具。本摘要的完善使用了AI工具。
查看英文原文 English abstract
Chimeric Antigen Receptor (CAR) T cell therapies have transformed cancer treatment, offering targeted and effective options for patients with hematologic B-cell malignancies, including leukemias, lymphomas and multiple myeloma. Their precision in targeting and eliminating cancer cells has positioned them as a promising approach in cellular immunotherapy. Accurate detection of CAR expression is essential for research, pre-clinical applications, clinical manufacturing, and patient immunomonitoring. To address these needs, we developed CAR Detection Reagents optimized for flow cytometric analysis of CAR-engineered T and NK cells, ensuring exceptional quality and specificity. Our recombinant antigen-based CAR Detection Reagents mimic CAR interactions with tumor cells, targeting key cell surface antigens such as CD19, BCMA, CD22, MSLN, CD123, B7-H3, HER2, and CD33. We also created anti-CAR antibodies for CD19 FMC63 and GD2 14G2a CARs, along with linker-specific antibodies for G4S- and Whitlow-linkers, commonly used in commercial CAR T cell products. All these reagents feature an engineered human IgG1 Fc region to prevent Fcgamma receptor binding, ensuring background-free analysis. Available in various conjugates (e.g., fluorophores, biotin), they offer superior performance and flexibility in panel design. Our flow cytometric analysis demonstrated bright and specific staining with low background on primary CAR T/NK cells and model cell lines, crucial for reliable CAR T cell enumeration in product manufacturing and patient monitoring. CAR Detection Reagents are also applicable for magnetic activated cell sorting (MACS). In immunomonitoring post-adoptive cell transfer, rapid isolation of CAR T cells from blood or PBMCs can be critical, as CAR T cells in these samples can be present in very low numbers falling below the detection limit. Magnetic enrichment substantially enhances analytical sensitivity, ensuring long-term monitoring of CAR T cell persistence, vital for assessing treatment efficacy and patient response. Furthermore, MACS-purified CAR T cells can undergo deep phenotyping and functional assays. Detecting CAR T cells in tissue samples is essential for understanding their distribution and activity within the body. This capability allows researchers and clinicians to assess CAR T cell infiltration and therapeutic impact at tumor sites, offering insights into treatment effectiveness and resistance mechanisms. Using fluorescence microscopy, we demonstrate precise detection and enumeration of CD19 FMC63 CAR T cells with a FMC63-targeting anti-CD19 CAR antibody in fresh-frozen and PFA-fixed tissue samples from treated mice. This approach enhances our understanding of CAR T cell dynamics in vivo . In summary, these versatile CAR Detection Reagents are invaluable tools for advancing CAR T cell research and clinical therapies. AI tools were used to improve this abstract.
利益披露 Disclosure
S. Wilmes, Miltenyi Biotec B.V. & Co. KG Employment. D. Missing, Miltenyi Biotec B.V. & Co. KG Employment. A. Brauchle, Miltenyi Biotec B.V. & Co. KG Employment. N. Borgelt, Miltenyi Biotec B.V. & Co. KG Employment. J. Müllers, Miltenyi Biotec B.V. & Co. KG Employment. M. Winkels, Miltenyi Biotec B.V. & Co. KG Employment. L. Möckel, Miltenyi Biotec B.V. & Co. KG Employment. M. Niemöller, Miltenyi Biotec B.V. & Co. KG Employment. D. Häußler-Kuballa, Miltenyi Biotec B.V. & Co. KG Employment. F. A. Bertram, Miltenyi Biotec B.V. & Co. KG Employment. O. Goldbach, Miltenyi Biotec B.V. & Co. KG Employment. D. Poschen, Miltenyi Biotec B.V. & Co. KG Employment. A. Imann, Miltenyi Biotec B.V. & Co. KG Employment. S. Rüberg, Miltenyi Biotec B.V. & Co. KG Employment. A. Appelshoffer, Miltenyi Biotec B.V. & Co. KG Employment. F. El Yassouri, Miltenyi Biotec B.V. & Co. KG Employment. M. Mues, Miltenyi Biotec B.V. & Co. KG Employment. V. Nölle, Miltenyi Biotec B.V. & Co. KG Employment. A. Bosio, Miltenyi Biotec B.V. & Co. KG Employment. C. Dose, Miltenyi Biotec B.V. & Co. KG Employment. A. Richter, Miltenyi Biotec B.V. & Co. KG Employment.

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