A120:反应性和非反应性同基因小鼠肿瘤模型的瘤内树突状细胞动力学

Huizhong Xiong, S. Mittman, Ryan Rodriguez, M. Moskalenko, P. Sanchez, Yagai Yang, R. Cubas
{"title":"A120:反应性和非反应性同基因小鼠肿瘤模型的瘤内树突状细胞动力学","authors":"Huizhong Xiong, S. Mittman, Ryan Rodriguez, M. Moskalenko, P. Sanchez, Yagai Yang, R. Cubas","doi":"10.1158/2326-6074.CRICIMTEATIAACR18-A120","DOIUrl":null,"url":null,"abstract":"Conventional dendritic cells (cDC) play a vital role in T-cell-mediated antitumor immunity by transporting and cross-presenting tumor antigens to CD8 T-cells in draining lymph nodes (dLN) and tumor tissue. DC maturation and antigen uptake takes place in the tumor, which can be heavily affected by the suppressive tumor microenvironment. Intratumoral DCs are a scarce population and their phenotypes and functions have not been fully understood. Here we thoroughly characterized cDC phenotypes and dynamics in a variety of commonly used syngeneic murine tumor models, both at baseline and following anti-PD-L1 (aPDL1) treatment to investigate the correlation and potential contribution of DCs to response. Surprisingly, we observed a lower density of intratumoral DCs in responsive tumor models when compared to nonresponsive ones and their abundance was further reduced by aPDL1 treatment in an IFNg-dependent manner. Their PDL1 expression levels, albeit lower than tumor macrophages, were positively correlated with response. These results demonstrate an inverse correlation between intratumoral DCs and aPDL1-mediated antitumor immunity across different syngeneic murine tumor models, and ongoing studies are exploring the fates of these intratumoral DCs with a focus on their causal relation with the efficacy of immunotherapy. Citation Format: Huizhong Xiong, Stephanie Mittman, Ryan Rodriguez, Marina Moskalenko, Patricia Pacheco Sanchez, Yagai Yang, Rafael Cubas. Intratumoral dendritic cell dynamics in responsive and nonresponsive syngeneic murine tumor models [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 A120.","PeriodicalId":22141,"journal":{"name":"Tackling the Tumor Microenvironment: Beyond T-cells","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2019-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Abstract A120: Intratumoral dendritic cell dynamics in responsive and nonresponsive syngeneic murine tumor models\",\"authors\":\"Huizhong Xiong, S. Mittman, Ryan Rodriguez, M. Moskalenko, P. Sanchez, Yagai Yang, R. Cubas\",\"doi\":\"10.1158/2326-6074.CRICIMTEATIAACR18-A120\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Conventional dendritic cells (cDC) play a vital role in T-cell-mediated antitumor immunity by transporting and cross-presenting tumor antigens to CD8 T-cells in draining lymph nodes (dLN) and tumor tissue. DC maturation and antigen uptake takes place in the tumor, which can be heavily affected by the suppressive tumor microenvironment. Intratumoral DCs are a scarce population and their phenotypes and functions have not been fully understood. Here we thoroughly characterized cDC phenotypes and dynamics in a variety of commonly used syngeneic murine tumor models, both at baseline and following anti-PD-L1 (aPDL1) treatment to investigate the correlation and potential contribution of DCs to response. Surprisingly, we observed a lower density of intratumoral DCs in responsive tumor models when compared to nonresponsive ones and their abundance was further reduced by aPDL1 treatment in an IFNg-dependent manner. Their PDL1 expression levels, albeit lower than tumor macrophages, were positively correlated with response. These results demonstrate an inverse correlation between intratumoral DCs and aPDL1-mediated antitumor immunity across different syngeneic murine tumor models, and ongoing studies are exploring the fates of these intratumoral DCs with a focus on their causal relation with the efficacy of immunotherapy. Citation Format: Huizhong Xiong, Stephanie Mittman, Ryan Rodriguez, Marina Moskalenko, Patricia Pacheco Sanchez, Yagai Yang, Rafael Cubas. Intratumoral dendritic cell dynamics in responsive and nonresponsive syngeneic murine tumor models [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 A120.\",\"PeriodicalId\":22141,\"journal\":{\"name\":\"Tackling the Tumor Microenvironment: Beyond T-cells\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Tackling the Tumor Microenvironment: Beyond T-cells\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1158/2326-6074.CRICIMTEATIAACR18-A120\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tackling the Tumor Microenvironment: Beyond T-cells","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1158/2326-6074.CRICIMTEATIAACR18-A120","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

传统树突状细胞(cDC)在t细胞介导的抗肿瘤免疫中发挥重要作用,通过将肿瘤抗原转运并交叉呈递到引流淋巴结(dLN)和肿瘤组织中的CD8 t细胞。DC成熟和抗原摄取发生在肿瘤中,这可能受到肿瘤微环境的严重影响。瘤内dc是一种罕见的种群,其表型和功能尚未完全了解。在这里,我们在各种常用的同基因小鼠肿瘤模型中,在基线和抗pd - l1 (aPDL1)治疗后,全面表征了cDC表型和动力学,以研究DCs与反应的相关性和潜在贡献。令人惊讶的是,与无反应的肿瘤模型相比,我们观察到应答性肿瘤模型中瘤内dc的密度较低,并且它们的丰度通过依赖ifng的方式通过aPDL1治疗进一步降低。它们的PDL1表达水平虽然低于肿瘤巨噬细胞,但与反应呈正相关。这些结果表明,在不同的同基因小鼠肿瘤模型中,肿瘤内dc与apdl1介导的抗肿瘤免疫之间存在负相关,并且正在进行的研究正在探索这些肿瘤内dc的命运,重点是它们与免疫治疗效果的因果关系。引文格式:熊慧忠,Stephanie Mittman, Ryan Rodriguez, Marina Moskalenko, Patricia Pacheco Sanchez, Yagai Yang, Rafael Cubas。反应性和非反应性同基因小鼠肿瘤模型的瘤内树突状细胞动力学[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 A120。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Abstract A120: Intratumoral dendritic cell dynamics in responsive and nonresponsive syngeneic murine tumor models
Conventional dendritic cells (cDC) play a vital role in T-cell-mediated antitumor immunity by transporting and cross-presenting tumor antigens to CD8 T-cells in draining lymph nodes (dLN) and tumor tissue. DC maturation and antigen uptake takes place in the tumor, which can be heavily affected by the suppressive tumor microenvironment. Intratumoral DCs are a scarce population and their phenotypes and functions have not been fully understood. Here we thoroughly characterized cDC phenotypes and dynamics in a variety of commonly used syngeneic murine tumor models, both at baseline and following anti-PD-L1 (aPDL1) treatment to investigate the correlation and potential contribution of DCs to response. Surprisingly, we observed a lower density of intratumoral DCs in responsive tumor models when compared to nonresponsive ones and their abundance was further reduced by aPDL1 treatment in an IFNg-dependent manner. Their PDL1 expression levels, albeit lower than tumor macrophages, were positively correlated with response. These results demonstrate an inverse correlation between intratumoral DCs and aPDL1-mediated antitumor immunity across different syngeneic murine tumor models, and ongoing studies are exploring the fates of these intratumoral DCs with a focus on their causal relation with the efficacy of immunotherapy. Citation Format: Huizhong Xiong, Stephanie Mittman, Ryan Rodriguez, Marina Moskalenko, Patricia Pacheco Sanchez, Yagai Yang, Rafael Cubas. Intratumoral dendritic cell dynamics in responsive and nonresponsive syngeneic murine tumor models [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 A120.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
The Tumor Microenvironment: Methods and Protocols Abstract A113: Harnessing lymphoid organ neogenesis as a novel prognostic biomarker and therapeutic target Abstract A072: Calreticulin exposures by malignant blasts correlate with robust anticancer immunity and improved clinical outcome in AML patients Abstract A092: TAM receptors targeting unleashes antileukemic immunity and enables checkpoint blockade leading to eradication of leukemic cells Abstract A070: Virotherapy eradicates established melanoma by reprogramming the tumor microenvironment and engaging the adaptive immunity
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1