Shahamatdar Sahar, He Meng Xiao, Reyna Matthew A, Gusev Alexander, AlDubayan Saud H, Van Allen Eliezer M, Ramachandran Sohini
Center for Computational Molecular Biology, Brown University, Providence, RI 02912, USA; Department of Ecology and Evolutionary Biology, Brown University, Providence, RI 02912, USA.
Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA; Harvard Graduate Program in Biophysics, Boston, MA 02115, USA.
Cell Rep. 2020 Mar 3;30(9):2900-2908.e4. doi: 10.1016/j.celrep.2020.02.039.
The immune composition of the tumor microenvironment influences response and resistance to immunotherapies. While numerous studies have identified somatic correlates of immune infiltration, germline features that associate with immune infiltrates in cancers remain incompletely characterized. We analyze seven million autosomal germline variants in the TCGA cohort and test for association with established immune-related phenotypes that describe the tumor immune microenvironment. We identify one SNP associated with the amount of infiltrating follicular helper T cells; 23 candidate genes, some of which are involved in cytokine-mediated signaling and others containing cancer-risk SNPs; and networks with genes that are part of the DNA repair and transcription elongation pathways. In addition, we find a positive association between polygenic risk for rheumatoid arthritis and amount of infiltrating CD8 T cells. Overall, we identify multiple germline genetic features associated with tumor-immune phenotypes and develop a framework for probing inherited features that contribute to differences in immune infiltration.
肿瘤微环境的免疫组成会影响对免疫疗法的反应和抗性。尽管众多研究已确定了免疫浸润的体细胞相关性,但与癌症中免疫浸润相关的种系特征仍未得到充分表征。我们分析了TCGA队列中的700万个常染色体种系变体,并测试其与描述肿瘤免疫微环境的既定免疫相关表型的关联。我们鉴定出一个与浸润性滤泡辅助性T细胞数量相关的单核苷酸多态性(SNP);23个候选基因,其中一些参与细胞因子介导的信号传导,其他一些含有癌症风险SNP;以及与DNA修复和转录延伸途径中的基因组成的网络。此外,我们发现类风湿性关节炎的多基因风险与浸润性CD8 T细胞数量之间存在正相关。总体而言,我们鉴定出多个与肿瘤免疫表型相关的种系遗传特征,并开发了一个框架来探究导致免疫浸润差异的遗传特征。