期刊
FRONTIERS IN IMMUNOLOGY
卷 12, 期 -, 页码 -出版社
FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2021.797407
关键词
spinal chordoma; immune checkpoint molecules; quantitative immunofluorescence; HHLA2; PD-L1; tumor infiltrating lymphocytes
类别
资金
- National Natural Science Foundation of China [82003802, 81871821, 82002364]
- Natural Science Foundation of Hunan Province [2019JJ50542, 2021JJ40509]
- Project for Clinical Research of Hunan Provincial Health Commission [20201978, 20201962, 20201956]
- Innovation guidance plan of Hunan Provincial Department of science and technology [2018SK51611]
This study investigated the expression of PD-L1, HHLA2, B7H3, IDO-1, and Galectin-9 in spinal chordoma and their association with tumor infiltrating lymphocytes, clinicopathological characteristics, and patient survival. The results showed that HHLA2 and PD-L1 were commonly expressed in spinal chordoma and their coexpression independently predicted worse local recurrence-free survival and overall survival. In contrast, stromal levels of PD-L1 and Galectin-9 were associated with better prognosis. This study provides insights into the immunosuppressive mechanism in chordoma and may contribute to the development of improved immunotherapy approaches.
BackgroundImmunotherapy only achieves efficacy in some cancer patients, and less is known about other immune checkpoint molecules in chordoma. Here, we aimed to determine the expression of PD-L1, HHLA2, B7H3, IDO-1 and Galectin-9 in spinal chordoma and evaluated their association with tumor infiltrating lymphocytes (TILs), clinicopathological characteristics and survival of patients. MethodsUsing multiplexed quantitative immunofluorescence (QIF), we simultaneously measured the levels of five different immune checkpoint molecules and major TIL subsets in 92 human spinal chordoma samples. ResultsTumor HHLA2 and PD-L1 were positive in 80.0% and 86.0% of cases, respectively. However, B7H3, IDO-1 and Galectin-9 positivity on tumor cells were only seen in 21.0% of cases, despite all showing predominantly stromal expression. Coexpression of these QIF markers in the tumor compartment was scarcely detected except for PD-L1 and HHLA2, which was observed in 69.6% of cases. While tumoral HHLA2 and stromal B7H3 expressions were associated with an aggressive tumor phenotype, suppressive immune response (specifically including elevated PD-1(+) TILs level and decreased CD8(+) TIL density) and poor prognosis, stromal levels of PD-L1 and Galectin-9 predicted the opposite outcomes. Importantly, HHLA2 and PD-L1 coexpression on tumor cells independently predicted both worse local recurrence-free survival and overall survival. ConclusionThese data provide a better understanding of the immunosuppressive mechanism in chordoma and may be useful for the development of combination or novel immunotherapy approaches aiming to improve therapeutic efficacy and survival.
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