Murgaski Aleksandar, Bardet Pauline M R, Arnouk Sana M, Clappaert Emile J, Laoui Damya
Myeloid Cell Immunology Lab, VIB Center for Inflammation Research, 1050 Brussels, Belgium.
Lab of Cellular and Molecular Immunology, Vrije Universiteit Brussel, 1050 Brussels, Belgium.
Cancers (Basel). 2019 May 14;11(5):670. doi: 10.3390/cancers11050670.
Recent advances in cancer immunotherapy have mainly focused on re-activating T-cell responses against cancer cells. However, both priming and activation of effector T-cell responses against cancer-specific antigens require cross-talk with dendritic cells (DCs), which are responsible for the capturing, processing and presentation of tumour-(neo)antigens to T cells. DCs consequently constitute an essential target in efforts to generate therapeutic immunity against cancer. This review will discuss recent research that is unlocking the cancer-fighting potential of tumour-infiltrating DCs. First, the complexity of DCs in the tumour microenvironment regarding the different subsets and the difficulty of translating mouse data into equivalent human data will be briefly touched upon. Mainly, possible solutions to problems currently faced in DC-based cancer treatments will be discussed, including their infiltration into tumours, activation strategies, and antigen delivery methods. In this way, we hope to put together a broad picture of potential synergistic therapies that could be implemented to harness the full capacity of tumour-infiltrating DCs to stimulate anti-tumour immune responses in patients.
癌症免疫疗法的最新进展主要集中在重新激活针对癌细胞的T细胞反应。然而,效应T细胞针对癌症特异性抗原的致敏和激活都需要与树突状细胞(DC)进行相互作用,树突状细胞负责捕获、处理肿瘤(新)抗原并将其呈递给T细胞。因此,DC构成了产生抗癌治疗性免疫努力中的一个重要靶点。本综述将讨论最近揭示肿瘤浸润性DC抗癌潜力的研究。首先,将简要提及肿瘤微环境中DC在不同亚群方面的复杂性以及将小鼠数据转化为等效人类数据的困难。主要将讨论基于DC的癌症治疗目前面临的问题的可能解决方案,包括它们向肿瘤的浸润、激活策略和抗原递送方法。通过这种方式,我们希望勾勒出一幅潜在协同疗法的广阔图景,这些疗法可以被实施以充分利用肿瘤浸润性DC刺激患者抗肿瘤免疫反应的全部能力。