Wilson Douglas R, Jin Chong, Ibrahim Joseph G, Sun Wei
Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
J Am Stat Assoc. 2020;115(531):1055-1065. doi: 10.1080/01621459.2019.1654874. Epub 2019 Sep 16.
Immunotherapies have attracted lots of research interests recently. The need to understand the underlying mechanisms of immunotherapies and to develop precision immunotherapy regimens has spurred great interest in characterizing immune cell composition within the tumor microenvironment. Several methods have been developed to estimate immune cell composition using gene expression data from bulk tumor samples. However, these methods are not flexible enough to handle aberrant patterns of gene expression data, e.g., inconsistent cell type-specific gene expression between purified reference samples and tumor samples. We propose a novel statistical method for expression deconvolution called ICeD-T (Immune Cell Deconvolution in Tumor tissues). ICeD-T automatically identifies aberrant genes whose expression are inconsistent with the deconvolution model and down-weights their contributions to cell type abundance estimates. We evaluated the performance of ICeD-T versus existing methods in simulation studies and several real data analyses. ICeD-T displayed comparable or superior performance to these competing methods. Applying these methods to assess the relationship between immunotherapy response and immune cell composition, ICeD-T is able to identify significant associations that are missed by its competitors.
免疫疗法最近引起了众多研究兴趣。了解免疫疗法的潜在机制以及制定精准免疫治疗方案的需求,激发了人们对表征肿瘤微环境中免疫细胞组成的浓厚兴趣。已经开发了几种方法,利用来自肿瘤组织样本的基因表达数据来估计免疫细胞组成。然而,这些方法在处理基因表达数据的异常模式方面不够灵活,例如,纯化的参考样本和肿瘤样本之间细胞类型特异性基因表达不一致。我们提出了一种名为ICeD-T(肿瘤组织中的免疫细胞反卷积)的用于表达反卷积的新型统计方法。ICeD-T会自动识别那些表达与反卷积模型不一致的异常基因,并降低它们对细胞类型丰度估计的贡献。我们在模拟研究和多个实际数据分析中评估了ICeD-T与现有方法的性能。ICeD-T表现出与这些竞争方法相当或更优的性能。将这些方法应用于评估免疫治疗反应与免疫细胞组成之间的关系时,ICeD-T能够识别出其竞争对手遗漏的显著关联。