B201:巨噬细胞死亡途径的探索与开发:以结核分枝杆菌感染为模型

Ryan Zander, David M. Schauder, G. Xin, C. Nguyen, Xiaopeng Wu, W. Cui
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摘要

巨噬细胞可以影响肿瘤的发展及其对治疗的反应。然而,我们对巨噬细胞的激活和存活是如何被调节的以及如何被治疗性地调节缺乏充分的了解。为了解决这些问题,我们转向了可能影响这些过程演变的宿主-病原体相互作用:结核分枝杆菌(Mtb)感染,这是感染导致死亡的主要原因。一旦被巨噬细胞内化,结核分枝杆菌抵抗巨噬细胞的杀伤并在巨噬细胞内复制。最终,结核分枝杆菌感染导致巨噬细胞死亡,使病原体传播到其他细胞。为了探索结核分枝杆菌如何诱导巨噬细胞死亡以及巨噬细胞死亡如何影响宿主对结核分枝杆菌的防御,我们在RAW264.7巨噬细胞中进行了全基因组CRISPR-Cas9隐性遗传筛选。我们发现I型干扰素信号通路成分的缺失,包括IFN-α/β受体(IFNAR),延迟了mmb诱导的细胞死亡。已知结核分枝杆菌感染诱导巨噬细胞产生I型干扰素。我们的发现将I型干扰素信号通路与mmb诱导的巨噬细胞死亡直接联系起来。我们目前正在研究I型ifn诱导细菌刺激的巨噬细胞死亡的机制。与此同时,我们正在测试这一途径的阻断剂作为针对结核病的宿主定向治疗,并在mtb感染的小鼠中发现了抗ifnar1单抗的显著保护作用,无论该单抗是在感染之前还是之后给药。进一步探索抗ifnar单抗的保护作用可能会指向一种基于抗体的宿主定向治疗。感谢:我们感谢华盛顿大学R. Schreiber教授为获得抗ifnar单抗提供了便利。引文格式:Ryan Zander, David Schauder,辛刚,Christine Nguyen,吴晓鹏,崔卫国。巨噬细胞死亡途径的探索与开发:以结核分枝杆菌感染为模型[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 B201。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract B201: Exploration and exploitation of macrophage death pathways: Infection by Mycobacterium tuberculosis as a model
Macrophages can impact the development of tumors and their responses to therapy. However, we lack a full understanding of how macrophage activation and survival are regulated and might be therapeutically modulated. To address these questions, we turned to a host-pathogen interaction that is likely to have impacted the evolution of these processes: infection by Mycobacterium tuberculosis (Mtb), the leading cause of death from infection. Once internalized by macrophages, Mtb resists killing by macrophages and replicates within them. Ultimately, Mtb infection results in death of macrophages, allowing dissemination of the pathogen to other cells. To explore how Mtb induces macrophage cell death and how macrophage cell death might impact host defense against Mtb, we performed a genome-wide CRISPR-Cas9 recessive genetic screen in RAW264.7 macrophages. We discovered that the absence of components of the type I interferon signaling pathway, including the IFN-α/β receptor (IFNAR), delays Mtb-induced cell death. It is known that Mtb infection induces macrophages to produce type I interferon. Our finding directly links type I interferon signaling pathway and Mtb-induced macrophage death. We are currently working on the mechanism of the type I IFN-induced death of bacterially-stimulated macrophages. Meanwhile, we are testing blockers of this pathway as host-directed therapy against TB and have seen striking protective effects of anti-IFNAR1 mAb in Mtb-infected mice, whether the mAb is administered before or after infection. Further exploration of the protective effect of anti-IFNAR mAb could point to an antibody-based, host-directed therapy. Acknowledgment: We thank Prof. R. Schreiber, Washington University, for facilitating access to anti-IFNAR mAb. Citation Format: Ryan Zander, David Schauder, Gang Xin, Christine Nguyen, Xiaopeng Wu, Weiguo Cui. Exploration and exploitation of macrophage death pathways: Infection by Mycobacterium tuberculosis as a model [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 B201.
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