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检测针对 CAR-T 细胞的抗药物抗体的流式细胞术方法建立

英文原题:Development of a flow cytometry method to measure antidrug antibodies against CAR T cells.

查看英文原题

Development of a flow cytometry method to measure antidrug antibodies against CAR T cells.

PubMed 2026/04/11(内容时间) Immunohorizons

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中文摘要

嵌合抗原受体(CAR)T细胞疗法基于对患者自身T细胞受体的基因修饰。由此产生的CAR-T 细胞细胞毒性反应被重新导向针对特定的肿瘤抗原。这种创新的免疫疗法已成功用于治疗血液系统恶性肿瘤,并且也正在被开发为实体瘤的治疗方法。CAR-T 细胞可导致与宿主中不期望的免疫应答相关的免疫相关不良结局,范围从急性事件到随时间持续的事件,例如抗药物抗体(ADA)的产生,这可能影响CAR-T 细胞一旦施用于患者后的疗效和持续性。作为对药物治疗的应答而产生的ADA并非CAR-T 细胞所独有,其产生的证据早已被认可。虽然传统类型的分析旨在通过免疫测定方法测量ADA的存在,但当治疗剂是细胞时,使用流式细胞术方法已成为检测和定量针对CAR-T 细胞产品以及任何其他细胞疗法的ADA的显而易见的选择。

在此,我们展示了一种流式细胞术方法开发的结果,该方法使用CAR-T 细胞测量ADA,并通过一种测定法以剂量依赖性方式检测ADA样分子与CAR-T 细胞的结合。该方法允许对ADA进行定量,并确定临床样本中潜在ADA测量所需的测定值。

展开英文摘要原文

Chimeric antigen receptor (CAR) T cell therapies are based on the genetic modification of the T cell receptor of a patient's own T cells. The resulting CAR T cells cytotoxic response is redirected against a specific tumor antigen. This innovative immunotherapy has been used successfully to treat blood malignancies, and it is also being developed as treatment for solid tumors. CAR T cells can lead to immune related adverse outcomes associated with an unwanted immune response in the host, ranging from acute events to those sustained with time, such as antidrug antibody (ADA) development, which can impact the efficacy and persistence of the CAR T cells once administered to the patient.

The development of ADAs as response to a drug treatment is not exclusive to CAR T cells, and evidence of their production has been long acknowledged. While traditional types of analysis aim to measure the presence of ADAs by immunoassay methods, with the therapeutic agent being cells, the use of a flow cytometry approach has become the obvious choice for detection and quantification of ADAs against CAR T cells products, as well as any other cell therapies.

Here, we present the results of the development of a flow cytometry method to measure ADAs using CAR T cells with an assay to detect the binding of an ADA-like molecule to the CAR T cells in a dose-dependent manner. This method allowed for quantification of ADAs and determination of the assay values needed for potential ADA measurement in clinical samples.

论文信息

作者
Day G、Sánchez-Martín FJ、Seavers L、Cadwallader K、Morgado-García S
单位
Immunology and Immunotoxicology Department, Labcorp, Huntingdon, United Kingdom.United Kingdom
期刊
ImmunoHorizons2026 Apr 11
原文标识
PubMed 42033387 · DOI 10.1093/immhor/vlag011