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协调细胞邻里关系在结直肠癌侵袭前沿调控抗肿瘤免疫。

Coordinated Cellular Neighborhoods Orchestrate Antitumoral Immunity at the Colorectal Cancer Invasive Front.

机构信息

Department of Microbiology & Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA; Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.

Department of Microbiology & Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA; Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA; Department of Bioengineering, Stanford University School of Medicine, Stanford, CA 94305, USA.

出版信息

Cell. 2020 Sep 3;182(5):1341-1359.e19. doi: 10.1016/j.cell.2020.07.005. Epub 2020 Aug 6.

Abstract

Antitumoral immunity requires organized, spatially nuanced interactions between components of the immune tumor microenvironment (iTME). Understanding this coordinated behavior in effective versus ineffective tumor control will advance immunotherapies. We re-engineered co-detection by indexing (CODEX) for paraffin-embedded tissue microarrays, enabling simultaneous profiling of 140 tissue regions from 35 advanced-stage colorectal cancer (CRC) patients with 56 protein markers. We identified nine conserved, distinct cellular neighborhoods (CNs)-a collection of components characteristic of the CRC iTME. Enrichment of PD-1CD4 T cells only within a granulocyte CN positively correlated with survival in a high-risk patient subset. Coupling of tumor and immune CNs, fragmentation of T cell and macrophage CNs, and disruption of inter-CN communication was associated with inferior outcomes. This study provides a framework for interrogating how complex biological processes, such as antitumoral immunity, occur through concerted actions of cells and spatial domains.

摘要

抗肿瘤免疫需要免疫肿瘤微环境(iTME)的各个组成部分进行有组织、空间细微的相互作用。了解在有效和无效肿瘤控制中这种协调行为将推进免疫疗法的发展。我们通过索引对石蜡包埋组织微阵列的共检测(CODEX)进行了重新设计,使我们能够同时对 35 名晚期结直肠癌(CRC)患者的 140 个组织区域进行 56 种蛋白质标志物的分析。我们确定了九个保守的、不同的细胞邻里(CNs)——一组CRC iTME 的特征成分。只有在粒细胞 CN 中 PD-1CD4 T 细胞的富集与高危患者亚组的生存呈正相关。肿瘤和免疫 CNs 的偶联、T 细胞和巨噬细胞 CNs 的碎片化以及 CN 之间的通讯中断与较差的结果相关。这项研究为研究抗肿瘤免疫等复杂的生物学过程如何通过细胞和空间域的协同作用发生提供了一个框架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5241/7479520/0d5e881c1752/fx1.jpg

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