期刊
ONCOLOGY
卷 100, 期 8, 页码 419-428出版社
KARGER
DOI: 10.1159/000525239
关键词
Liver cancer; Foxp3; Co-stimulatory receptor; Tumor microenvironment; Immunotherapy; Immune checkpoint
类别
资金
- Ministry of Science and Technology, Taiwan [MOST 108-2314-B-002-073, 1092314-B-002-225, 110-2314-B-002-204-MY3]
- Good Liver Foundation
This study revealed the clinical significance of ICOS-expressing Tregs in hepatocellular carcinoma (HCC). The presence of high-density ICOS+ Tregs in the tumor center and their close proximity to other ICOS+ cells suggested a strong immunosuppressive tumor microenvironment. Furthermore, a high proportion of ICOS+Foxp(3+) cells and shorter distances between ICOS+ Tregs and other ICOS+ cells were associated with poor overall survival, highlighting the potential clinical benefit of depleting ICOS+ Tregs in HCC patients.
Introduction: Inducible co-stimulator (ICOS), an important co-stimulatory receptor on effector T cells (Teffs), may also contribute to tumor growth due to its high expression on regulatory T cells ( Tregs). This study explored the clinical significance of ICOS-expressing Tregs in hepatocellular carcinoma (HCC). Methods: Tumor tissues from HCC patients who received curative hepatectomy were obtained at a referral center. Dual immunohistochemistry was performed to evaluate the expression of ICOS and Foxp3. The cell densities and proximities between stained cells in regions of interest were measured by digital pathology and the associations with clinical outcome were analyzed. Results: A total of 142 patients ( male:female = 112: 30, median age of 61.0 years) were enrolled. Among them, 87 (61.3%) had chronic hepatitis B virus infection and 33 (23.2%) had chronic hepatitis C infection. Low a-fetoprotein level (< 20 ng/mL) and early- stage were significantly associated with improved overall survival (OS). The density of ICOS+Foxp(3+) cells and the ratio of ICOS+Foxp(3+)/total Foxp(3+) cells were significantly higher (p < 0.001) in the tumor center than in the peritumor area. Patients with a high density of ICOS+Foxp(3+) cells or a high ratio of ICOS+Foxp(3+)/total Foxp(3+) cells in the tumor center trended to have a shorter OS. A shorter distance between ICOS+Foxp(3+) cells and ICOS+Foxp(3-) cells (likely Teffs) in the tumor center was significantly associated with a shorter OS (p = 0.030), suggesting active immunosuppression of ICOS+ Tregs on ICOS+ Teffs. Conclusion: An increased abundance of ICOS+ Tregs in the tumor center in comparison to the peritumor area indicates a strong immunosuppressive tumor microenvironment of HCC. A high proportion of ICOS+Foxp(3+) cells and a shorter distance between ICOS+ Tregs and other ICOS+ cells were associated with a poor OS, suggesting that depleting ICOS+ Tregs might provide clinical benefit for patients with HCC.
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