Yuan Jiajia, Zhao Xingwang, Li Yanyan, Yao Qian, Jiang Lei, Feng Xujiao, Shen Lin, Li Yilin, Chen Yang
Department of Gastrointestinal Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital and Institute, Beijing 100142, China.
Department of Pathology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital and Institute, Beijing 100142, China.
Cancers (Basel). 2022 Jul 25;14(15):3608. doi: 10.3390/cancers14153608.
The tumor microenvironment plays a vital role in tumor progression and treatment response. However, the association between immune cell concentrations in primary tumor and blood indexes remains unknown. Thus, we enrolled patients with gastric cancer (GC) in two cohorts. We used multiplexed immunohistochemistry to quantify in situ proteins covering rare cell types at sub-cellular resolution in 80 patients with GC in the first cohort. A high correlation between the LMR (lymphocyte-to-monocyte ratio)/NLR (neutrophil-to-lymphocyte ratio) and tumor immune microenvironment was found. The density of exhausted CD8 T cells including CD8+PD1−TIM3+, CD8+LAG3+PD1+, CD8+LAG3+PD1−, CD8+LAG3+PD1+TIM3− was negatively associated with LMR and positively associated with NLR (p < 0.05). Additionally, the higher density of macrophages in tumor core was associated with a higher platelet-to-lymphocyte ratio and systemic immune-inflammation index. Furthermore, we validated the prognostic value of LMR and NLR in an independent cohort of 357 gastric cancer patients receiving immunotherapy. Higher LMR at baseline was significantly associated with superior immune-related PFS (irPFS) and a trend of superior immune-related OS (irOS). Higher NLR was associated with inferior irOS. In conclusion, blood indexes were associated with immune cells infiltrating in primary tumors of GC. NLR and LMR are associated with the density of exhausted CD8+ T immune cells, which leads to prognostic values of immunotherapy.
肿瘤微环境在肿瘤进展和治疗反应中起着至关重要的作用。然而,原发性肿瘤中免疫细胞浓度与血液指标之间的关联尚不清楚。因此,我们将胃癌(GC)患者纳入两个队列。在第一个队列的80例GC患者中,我们使用多重免疫组化在亚细胞分辨率下对涵盖稀有细胞类型的原位蛋白进行定量。发现淋巴细胞与单核细胞比率(LMR)/中性粒细胞与淋巴细胞比率(NLR)与肿瘤免疫微环境之间存在高度相关性。包括CD8 + PD1−TIM3 +、CD8 + LAG3 + PD1 +、CD8 + LAG3 + PD1−、CD8 + LAG3 + PD1 + TIM3−在内的耗竭CD8 T细胞密度与LMR呈负相关,与NLR呈正相关(p < 0.05)。此外,肿瘤核心中巨噬细胞的较高密度与较高的血小板与淋巴细胞比率和全身免疫炎症指数相关。此外,我们在接受免疫治疗的357例胃癌患者的独立队列中验证了LMR和NLR的预后价值。基线时较高的LMR与优越的免疫相关无进展生存期(irPFS)以及优越的免疫相关总生存期(irOS)趋势显著相关。较高的NLR与较差的irOS相关。总之,血液指标与GC原发性肿瘤中浸润的免疫细胞相关。NLR和LMR与耗竭的CD8 + T免疫细胞密度相关,这导致了免疫治疗的预后价值。