PROTAC 工程化蛋白/DNA 纳米抗原是癌症免疫治疗中树突状细胞疫苗的有效增强剂
PROTAC-Engineered Protein/DNA Nanoantigen is a Potent Booster for Dendritic Cell Vaccines in Cancer Immunotherapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Dendritic Cell Therapy in Immuno-Oncology: A Potentially Key Component of Anti-Cancer Immunotherapies.
Dendritic Cell Therapy in Immuno-Oncology: A Potentially Key Component of Anti-Cancer Immunotherapies.
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树突状细胞(DCs)是一个异质性群体,以抗原提呈和免疫调节著称,在启动针对病原体和肿瘤细胞的T细胞应答中发挥关键作用。尽管其具有推定的治疗价值,但外周血中DCs的稀少限制了其直到最近才在治疗应用中的直接使用。
然而,DCs可在体外从循环单核细胞中生成这一发现,推动了DCs在临床应用中的广泛研究。尽管如此,尽管已有大量临床试验,DCs进入日常临床肿瘤学实践仍被延迟。在这篇叙述性综述中,我们提供了该领域的最新总结,涵盖DCs用于过继性细胞免疫治疗概念的理论和实践方面,以及这些细胞在临床肿瘤学实践中已完成或正在进行的临床试验。为了更好地理解该领域的当前进展,我们纳入了截至当时已发表可评估数据的临床试验报告。根据我们的文献调查,基于DCs的过继性细胞治疗是一种安全的治疗干预,具有有价值的临床潜力。
然而,其广泛实施可能因若干因素而被延迟,这些因素使对临床试验结果的有意义评估变得复杂。这些因素包括临床前试验概念种类繁多、患者队列难以处理且异质性大,以及所应用的干预技术多样。由于这些因素可能阻碍基于DCs的应用以更广泛形式在免疫治疗中的常规实施,因此一个紧迫的近期未来方向似乎是基于DCs方法的标准化。
Dendritic cells (DCs) are a heterogeneous population known for antigen presentation and immune modulation, playing a key role in priming a T cell response against pathogens and tumor cells. Despite their putative therapeutic value, their scarcity in peripheral blood limited their direct use in therapeutic applications until recently. The discovery that DCs can be generated from circulating monocytes ex vivo, however, gave a boost of extensive research in the use of DCs in clinical applications. Still, despite the numerous clinical trials, the introduction of DCs in the everyday clinical oncology practice is delayed. In this narrative review, we provide an updated summary of the field covering the theoretical and practical aspects of the concept of the use of DCs in adoptive cellular immunotherapy and the completed or ongoing clinical trials for the use of these species in clinical oncology practice.
To better understand the current developments of the field, we included those clinical trial reports that published evaluable data to date. Based on our literature survey, DC-based adoptive cellular therapy is a safe therapeutic intervention with valuable clinical potential. Its widespread implementation, however, is likely delayed due to a number of factors that make meaningful evaluation of clinical trial results complicated.
These include the great variety of preclinical trial concepts, difficult and heterogenous patient cohorts, and the diversity of intervention techniques applied. Since these factors might hinder the routine implementation of DC-based applications in the more widespread forms of immunotherapy, one of the urgent short-term future directions seems to be the standardization of the DC-based methodologies.
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