通过靶向肿瘤相关巨噬细胞的嵌合受体工程化溶瘤病毒重振内源性抗肿瘤免疫
Rejuvenating endogenous antitumor immunity via a chimeric receptor-engineered oncolytic virus targeting tumor-associated macrophages.
我们的研究结果定义了一个精准溶瘤平台,该平台能够解除 TAM 介导的免疫抑制,同时增强适应性免疫,为癌症免疫治疗提供了一条有前景的转化途径。
英文原题:ELISPOT as a Functional for Biomarker Study in Cancer Immunotherapy: Applications and Future Directions.
ELISPOT as a Functional for Biomarker Study in Cancer Immunotherapy: Applications and Future Directions.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
本系统综述对 78 项研究进行了结构化定性综合,这些研究探讨了 ELISPOT 在癌症免疫治疗中的应用,包括癌症疫苗、溶瘤病毒、细胞疗法、免疫检查点抑制剂和生物标志物开发。
酶联免疫斑点(ELISPOT)试验是一种高灵敏度且广泛使用的技术,用于评估癌症研究中的抗原特异性细胞免疫应答。通过在单细胞水平上定量细胞因子分泌,特别是干扰素γ(IFN-γ),ELISPOT提供了T细胞活性的功能性读数,在临床前和临床环境中均有应用。本系统综述对78项研究进行了结构化定性综合,这些研究探讨了ELISPOT在癌症免疫治疗中的应用,包括癌症疫苗、溶瘤病毒、细胞疗法、免疫检查点抑制剂和生物标志物开发。研究按照PRISMA指南从PubMed、Scopus和Embase中筛选,重点关注具有转化相关性的临床和临床前研究。证据表明,ELISPOT被广泛用于验证肿瘤相关抗原和新抗原,监测癌症免疫治疗(包括免疫检查点阻断、癌症疫苗和过继细胞疗法)过程中的抗原特异性T细胞应答,以及表征抗原特异性T细胞功能。然而,仅有有限的一部分研究建立了ELISPOT应答与临床有意义结局之间的直接关联。此外,试验方案和报告标准的显著差异限制了跨研究的可比性和可重复性。总体而言,ELISPOT仍然是癌症研究中免疫监测的有价值工具。但其作为临床验证生物标志物的实施需要进一步的标准化、前瞻性验证以及与互补分析方法的整合。
The Enzyme-Linked ImmunoSpot (ELISPOT) assay is a highly sensitive and widely used technique for assessing antigen-specific cellular immune responses in cancer research. By enabling the quantification of cytokine secretion at the single-cell level, particularly interferon gamma (IFN-γ), ELISPOT provides a functional readout of T cell activity with applications in both preclinical and clinical settings. This systematic review presents a structured qualitative synthesis of 78 studies investigating the use of ELISPOT in cancer immunotherapy, including cancer vaccines, oncolytic viruses, cellular therapies, immune checkpoint inhibitors, and biomarker development. Studies were selected following PRISMA guidelines from PubMed, Scopus, and Embase, focusing on both clinical and preclinical research with translational relevance. The evidence indicates that ELISPOT is widely used to validate tumor-associated antigens and neoantigens, monitor antigen-specific T cell responses during cancer immunotherapy, including immune checkpoint blockade, cancer vaccines, and adoptive cell therapies, and characterize antigen-specific T cell function. However, only a limited subset of studies establishes direct associations between ELISPOT responses and clinically meaningful outcomes. In addition, substantial variability in assay protocols and reporting criteria limits cross-study comparability and reproducibility. Overall, ELISPOT remains a valuable tool for immune monitoring in cancer research. Still, its implementation as a clinically validated biomarker requires further standardization, prospective validation, and integration with complementary analytical approaches.
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