IL18 Receptor Signaling Regulates Tumor-Reactive CD8+ T-cell Exhaustion via Activation of the IL2/STAT5/mTOR Pathway in a Pancreatic Cancer Model

细胞毒性T细胞 癌症研究 生物 CD8型 PI3K/AKT/mTOR通路 T细胞 肿瘤微环境 过继性细胞移植 信号转导 细胞生物学 免疫学 免疫系统 生物化学 体外
作者
Veronika Lutz,Veronique M. Hellmund,Felix S.R. Picard,Hartmann Raifer,Teresa Ruckenbrod,Matthias Klein,Tobias Bopp,Rajkumar Savai,Peter Duewell,Corinna U. Keber,Andreas Weigert,Ho‐Ryun Chung,Malte Buchholz,André Menke,Thomas M. Gress,Magdalena Huber,Christian Bauer
出处
期刊:Cancer immunology research [American Association for Cancer Research]
卷期号:11 (4): 421-434 被引量:48
标识
DOI:10.1158/2326-6066.cir-22-0398
摘要

Abstract Intratumoral cytotoxic CD8+ T cells (CTL) enter a dysfunctional state characterized by expression of coinhibitory receptors, loss of effector function, and changes in the transcriptional landscape. Even though several regulators of T-cell exhaustion have been identified, the molecular mechanisms inducing T-cell exhaustion remain unclear. Here, we show that IL18 receptor (IL18R) signaling induces CD8+ T-cell exhaustion in a murine pancreatic cancer model. Adoptive transfer of Il18r−/− OT-1 CD8+ CTLs resulted in enhanced rejection of subcutaneous tumors expressing ovalbumin (OVA) as a model antigen (PancOVA), compared with wild-type OT-1 CTLs. Transferred intratumoral IL18R-deficient CTLs expressed higher levels of effector cytokines TNF and IFNγ and had reduced expression of coinhibitory receptors (PD-1, TIM-3, 2B4, LAG-3) and the transcription factors Eomes and TOX. Lower expression of coinhibitory receptors and TOX on IL18R-deficient versus IL18R-sufficient CD8+ T cells were confirmed in an orthotopic KPC model. IL18R-induced T-cell exhaustion was regulated by IL2/STAT5 and AKT/mTOR pathways, as demonstrated in an in vitro exhaustion assay. Concordantly, mice deficient in NLRP3, the molecular complex activating IL18, had decreased expression of coinhibitory receptors on intratumoral T cells and similar changes in signaling pathways at the transcriptome level. Thus, molecular pathways promoting T-cell exhaustion indicate an involvement of an NLRP3-expressing tumor microenvironment, which mediates IL18 release. The Cancer Genome Atlas analysis of patients with pancreatic carcinoma showed an association between NLRP3-mediated IL18 signaling and shorter survival. These findings indicate NLRP3-mediated IL18R signaling as a regulator of intratumoral T-cell exhaustion and a possible target for immunotherapy. Watch the interview with Veronika Lutz, PhD, and Christian Bauer, MD, corecipients of the 2025 Cancer Immunology Research Award for Outstanding Journal Article: https://vimeo.com/1100470935 See related Spotlight by Stromnes, p. 400
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