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溶瘤疫苗接种后肿瘤抗原特异性T细胞反应的检测

Detection of Tumor Antigen-Specific T-Cell Responses After Oncolytic Vaccination.

作者信息

Pol Jonathan G, Bridle Byram W, Lichty Brian D

机构信息

Gustave Roussy Comprehensive Cancer Institute, Villejuif, France.

INSERM, U1138, Paris, France.

出版信息

Methods Mol Biol. 2020;2058:191-211. doi: 10.1007/978-1-4939-9794-7_12.

Abstract

Oncolytic vaccines, which consist of recombinant oncolytic viruses (OV) encoding tumor-associated antigens (TAAs), have demonstrated potent antitumor efficacy in preclinical models and are currently evaluated in phase I/II clinical trials. On one hand, oncolysis of OV-infected malignant entities reinstates cancer immunosurveillance. On the other hand, overexpression of TAAs in infected cells further stimulates the adaptive arm of antitumor immunity. Particularly, the presence of tumor-specific CD8 T lymphocytes within the tumor microenvironment, as well as in the periphery, has demonstrated prognostic value for cancer treatments. These effector CD8 T cells can be detected through their production of the prototypical Tc1 cytokine: IFN-γ. The quantitative and qualitative assessment of this immune cell subset remains critical in the development process of efficient cancer vaccines, including oncolytic vaccines. The present chapter will describe a single-cell immunological assay, namely the intracellular cytokine staining (ICS), that allows the enumeration of IFN-γ-producing TAA-specific CD8 T cells in various tissues (tumor, blood, lymphoid organs) following oncolytic vaccination.

摘要

溶瘤疫苗由编码肿瘤相关抗原(TAA)的重组溶瘤病毒(OV)组成,已在临床前模型中显示出强大的抗肿瘤功效,目前正在进行I/II期临床试验评估。一方面,被OV感染的恶性实体的溶瘤作用恢复了癌症免疫监视。另一方面,感染细胞中TAA的过表达进一步刺激了抗肿瘤免疫的适应性分支。特别是,肿瘤微环境以及外周中肿瘤特异性CD8 T淋巴细胞的存在已证明对癌症治疗具有预后价值。这些效应性CD8 T细胞可通过其产生典型的Tc1细胞因子:IFN-γ来检测。在包括溶瘤疫苗在内的高效癌症疫苗的开发过程中,对这一免疫细胞亚群进行定量和定性评估仍然至关重要。本章将描述一种单细胞免疫测定方法,即细胞内细胞因子染色(ICS),该方法可在溶瘤疫苗接种后对各种组织(肿瘤、血液、淋巴器官)中产生IFN-γ的TAA特异性CD8 T细胞进行计数。

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