促炎异体树突状细胞促进旁观者免疫细胞的激活,间接激活抗原特异性t细胞

G. Fotaki, Chuan Jin, I. Kerzeli, Mohanraj Ramachandran, A. Karlsson-Parra, Di Yu, M. Essand
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引用次数: 0

摘要

体外修饰的自体患者源性树突状细胞(dc)可呈递肿瘤相关抗原,常被用作癌症疫苗。然而,除了在患者基础上生产树突状细胞的严格后勤外,越来越多的证据表明,这种树突状细胞迁移能力差,实际上在体内不直接与幼稚t细胞相互作用。相反,它是旁观者宿主dc从凋亡疫苗dc中获取物质,随后启动抗肿瘤t细胞反应。我们研究了利用同种异体促炎dc (allodc)作为免疫增强剂的可能性,它可能影响旁观者免疫细胞的激活并促进抗原特异性t细胞反应。我们已经证实了用成熟鸡尾酒结合感染增强腺病毒成熟的树突状细胞的炎症状态。这种促炎异源细胞在体外表达共刺激和激活分子,分泌Th-1型细胞因子。T细胞和NK细胞与这些同种异体dc共培养后上调活化标记物,并创造了一个免疫刺激环境,该环境被发现可以促进抗原负载dc的成熟,并通过交叉呈递促进抗原特异性T细胞的激活。我们的发现在小鼠模型中作为一种治疗策略进行了成功的评估。我们建议,将促炎同种异体细胞与Ad5M联合使用作为可能的抗原递送载体,可能是一种具有成本效益的诱导抗肿瘤免疫反应的策略。引文格式:Grammatiki Fotaki, Chuan Jin, Iliana Kyriaki Kerzeli, Mohanraj Ramachandran, Alex Karlsson-Parra, Di Yu, Magnus Essand。促炎异体树突状细胞促进旁观者免疫细胞的激活并间接许可抗原特异性t细胞[摘要]。第四届CRI-CIMT-EATI-AACR国际癌症免疫治疗会议:将科学转化为生存;2018年9月30日至10月3日;纽约,纽约。费城(PA): AACR;癌症免疫学杂志,2019;7(2增刊):摘要nr B110。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract B110: Proinflammatory allogeneic dendritic cells promote activation of bystander immune cells and indirectly license antigen-specific T-cells
Autologous patient-derived dendritic cells (DCs) modified ex vivo to present tumor-associated antigens have frequently been utilized as cancer vaccines. However, apart from the stringent logistics in producing DCs on a patient basis, accumulating evidences indicate that such DCs are poor in migration and in fact do not directly interact with naive T-cells in vivo. Instead, it is the bystander host-DCs taking up material from apoptotic vaccine DCs and subsequently initiate antitumor T-cell responses. We examine the possibility of harnessing allogeneic pro-inflammatory DCs (alloDCs) as immune enhancers which may affect the activation of bystander immune cells and promote antigen-specific T-cell responses. We have verified the inflammatory state of DCs matured with a maturation cocktail in combination with an infection-enhanced adenovirus. Such proinflammatory alloDCs expressed co-stimulatory and activation molecules and secreted Th-1 type cytokines in vitro. T and NK cells up-regulated activation markers after co-culture with such alloDCs and created an immunostimulatory environment which was found to promote maturation of antigen-loaded DCs and the subsequent activation of antigen-specific T-cells by cross-presentation. Our findings were evaluated as a therapeutic strategy in murine models with success. We are proposing that vaccination with proinflammatory alloDCs in combination with the use of Ad5M as possible antigen delivery vehicle can be a cost-effective strategy to induce antitumor immune responses. Citation Format: Grammatiki Fotaki, Chuan Jin, Iliana Kyriaki Kerzeli, Mohanraj Ramachandran, Alex Karlsson-Parra, Di Yu, Magnus Essand. Proinflammatory allogeneic dendritic cells promote activation of bystander immune cells and indirectly license antigen-specific T-cells [abstract]. In: Proceedings of the Fourth CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; Sept 30-Oct 3, 2018; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2019;7(2 Suppl):Abstract nr B110.
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