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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:A Toolkit for Profiling the Immune Landscape of Pediatric Central Nervous System Malignancies.
A Toolkit for Profiling the Immune Landscape of Pediatric Central Nervous System Malignancies.
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儿童中枢神经系统(CNS)恶性肿瘤的预后仍然很差,原因是治疗选择有限,导致高死亡率和长期并发症。免疫疗法,包括检查点抑制、癌症疫苗、工程化T细胞疗法和溶瘤病毒,在一些血液系统恶性肿瘤和实体瘤中已显示出有希望的结果,并正在各种高级别CNS恶性肿瘤的临床试验中进行研究。
然而,对于儿童病例,肿瘤免疫微环境(TIME)在CNS恶性肿瘤中的作用大多未知。为了成功实施免疫疗法并最终预测哪些患者会从这些治疗中获益,对诊断时及整个治疗过程中的TIME进行深入表征至关重要。在这篇综述中,我们概述了CNS恶性肿瘤免疫分析的技术,并详细说明了如何将这些技术用于不同的组织类型和研究。这些技术包括用于定量和表型分析浸润免疫细胞的免疫组织化学和流式细胞术、用于描述相关免疫通路的bulk和单细胞转录组学,以及功能测定。
最后,我们旨在描述评估癌症治疗涉及的其他免疫系统区室的潜在益处,例如脑脊液和血液,以及此类液体活检在设计免疫监测研究时如何提供信息。理解和统一评估儿童CNS恶性肿瘤的TIME和免疫景观,对于最终将免疫疗法整合到临床实践中至关重要。
The prognosis of pediatric central nervous system (CNS) malignancies remains dismal due to limited treatment options, resulting in high mortality rates and long-term morbidities. Immunotherapies, including checkpoint inhibition, cancer vaccines, engineered T cell therapies, and oncolytic viruses, have promising results in some hematological and solid malignancies, and are being investigated in clinical trials for various high-grade CNS malignancies.
However, the role of the tumor immune microenvironment (TIME) in CNS malignancies is mostly unknown for pediatric cases. In order to successfully implement immunotherapies and to eventually predict which patients would benefit from such treatments, in-depth characterization of the TIME at diagnosis and throughout treatment is essential.
In this review, we provide an overview of techniques for immune profiling of CNS malignancies, and detail how they can be utilized for different tissue types and studies. These techniques include immunohistochemistry and flow cytometry for quantifying and phenotyping the infiltrating immune cells, bulk and single-cell transcriptomics for describing the implicated immunological pathways, as well as functional assays.
Finally, we aim to describe the potential benefits of evaluating other compartments of the immune system implicated by cancer therapies, such as cerebrospinal fluid and blood, and how such liquid biopsies are informative when designing immune monitoring studies. Understanding and uniformly evaluating the TIME and immune landscape of pediatric CNS malignancies will be essential to eventually integrate immunotherapy into clinical practice.
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