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Tumour-derived exosomes as antigen delivery carriers in dendritic cell-based immunotherapy for malignant mesothelioma

机译:肿瘤来源的外来体在基于树突细胞的恶性间皮瘤免疫治疗中作为抗原传递载体

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摘要

BackgroundIn 2001, it was postulated that tumour-derived exosomes could be a potent source of tumour-associated antigens (TAA). Since then, much knowledge is gained on their role in tumorigenesis but only very recently tumour-derived exosomes were used in dendritic cell (DC)-based immunotherapy. For this, DCs were cultured ex-vivo and loaded with exosomes derived from immunogenic tumours such as melanoma or glioma and re-administrated to induce anti-tumour responses in primary and metastatic tumour mouse models. In contrast, malignant mesothelioma (MM) is a non-immunogenic tumour and because only a few mesothelioma-specific TAA are known to date, we investigated whether mesothelioma-derived exosomes could be used as antigen source in DC-based immunotherapy.
机译:背景2001年,有人推测肿瘤来源的外来体可能是肿瘤相关抗原(TAA)的有效来源。从那时起,人们就它们在肿瘤发生中的作用获得了许多知识,但是直到最近,基于肿瘤的外泌体才被用于基于树突细胞(DC)的免疫治疗中。为此,将DCs离体培养并装载源自免疫原性肿瘤(例如黑素瘤或神经胶质瘤)的外泌体,并重新给药以在原发性和转移性肿瘤小鼠模型中诱导抗肿瘤反应。相比之下,恶性间皮瘤(MM)是一种非免疫原性肿瘤,并且由于迄今仅已知少数间皮瘤特异性TAA,因此我们调查了间皮瘤衍生的外来体是否可以用作基于DC的免疫治疗的抗原来源。

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