绘制遗传景观,建立有利于抗pd -1反应的肿瘤免疫微环境。

IF 7.5 1区 生物学 Q1 CELL BIOLOGY
Daniel A Skelly, John P Graham, Mingshan Cheng, Mayuko Furuta, Andrew Walter, Thomas A Stoklasek, Hongyuan Yang, Timothy M Stearns, Olivier Poirion, Ji-Gang Zhang, Jessica D S Grassmann, Diane Luo, William F Flynn, Elise T Courtois, Chih-Hao Chang, David V Serreze, Francesca Menghi, Laura G Reinholdt, Edison T Liu
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引用次数: 0

摘要

鉴定调节免疫检查点抑制剂(ICI)功效的宿主遗传因素在实验上具有挑战性。我们的方法,利用协作交叉小鼠遗传资源,固定肿瘤基因组配置,同时改变宿主遗传。我们发现,在四种不同的小鼠肿瘤模型中,抗pd -1 (aPD1)免疫治疗的反应具有显著的遗传性(H2: 0.18-0.40)。对于MC38结直肠癌系统,我们绘制了四个具有显著上位相互作用的重要ICI应答数量性状位点(qtl)。这些qtl中定义应答基因的差异表达基因在抗原加工和呈递、同种异体移植物排斥和移植物抗宿主病等过程中高度富集(均p < 1 × 10-10)。功能阻断两个主要候选免疫靶点GM-CSF和IL-2RB,完全消除MC38对aPD1治疗的转录应答。因此,我们的体内实验平台是发现宿主遗传因素建立肿瘤免疫微环境有利于ICI反应的有力途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mapping the genetic landscape establishing a tumor immune microenvironment favorable for anti-PD-1 response.

Identifying host genetic factors modulating immune checkpoint inhibitor (ICI) efficacy is experimentally challenging. Our approach, utilizing the Collaborative Cross mouse genetic resource, fixes the tumor genomic configuration while varying host genetics. We find that response to anti-PD-1 (aPD1) immunotherapy is significantly heritable in four distinct murine tumor models (H2: 0.18-0.40). For the MC38 colorectal carcinoma system, we map four significant ICI response quantitative trait loci (QTLs) with significant epistatic interactions. The differentially expressed genes within these QTLs that define responder genetics are highly enriched for processes involving antigen processing and presentation, allograft rejection, and graft vs. host disease (all p < 1 × 10-10). Functional blockade of two top candidate immune targets, GM-CSF and IL-2RB, completely abrogates the MC38 transcriptional response to aPD1 therapy. Thus, our in vivo experimental platform is a powerful approach for discovery of host genetic factors that establish the tumor immune microenvironment propitious for ICI response.

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来源期刊
Cell reports
Cell reports CELL BIOLOGY-
CiteScore
13.80
自引率
1.10%
发文量
1305
审稿时长
77 days
期刊介绍: Cell Reports publishes high-quality research across the life sciences and focuses on new biological insight as its primary criterion for publication. The journal offers three primary article types: Reports, which are shorter single-point articles, research articles, which are longer and provide deeper mechanistic insights, and resources, which highlight significant technical advances or major informational datasets that contribute to biological advances. Reviews covering recent literature in emerging and active fields are also accepted. The Cell Reports Portfolio includes gold open-access journals that cover life, medical, and physical sciences, and its mission is to make cutting-edge research and methodologies available to a wide readership. The journal's professional in-house editors work closely with authors, reviewers, and the scientific advisory board, which consists of current and future leaders in their respective fields. The advisory board guides the scope, content, and quality of the journal, but editorial decisions are independently made by the in-house scientific editors of Cell Reports.
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