TIGIT modulates sepsis-induced immune dysregulation in mice with preexisting malignancy

• Type of Material: Article
• Authors: Wenxiao Zhang, Emory University; Jerome C Anyalebechi, Emory University; Kimberly M Ramonell, Emory University; Ching-Wen Chen, Emory University; Jianfeng Xie, Emory University; Zhe Liang, Emory University; Deena B Chihade, Emory University; Shunsuke Otani, Emory University; Craig Coopersmith, Emory University; Mandy Ford, Emory University
• Language: English
• Date: 2021-06-08
• Publisher: AMER SOC CLINICAL INVESTIGATION INC
• Publication Version: Final Published Version
• Copyright Statement: © 2021, Zhang et al. This is an open access article published under the terms of the Creative Commons Attribution 4.0 International License.
• License: Creative Commons Attribution 4.0 International
• Final Published Version (URL): http://dx.doi.org/10.1172/jci.insight.139823
• Title of Journal or Parent Work: JCI INSIGHT
• Volume: 6
• Issue: 11
• Grant/Funding Information: This study was supported by grants T32GM095442, R01GM104323, R01AA027396, R01AI149274, R56 AI154895, and R01 GM072808 to CMC and MLF.
• Keywords: REGULATORY T-CELLS; IMPROVES SURVIVAL; Science & Technology; BURDEN; OUTCOMES; SEPTIC SHOCK; Medicine, Research & Experimental; MORTALITY; Research & Experimental Medicine; Life Sciences & Biomedicine; PD-1; APOPTOSIS
• Research Categories: Health Sciences, Medicine and Surgery

Abstract

TIGIT is a recently identified coinhibitory receptor that is upregulated in the setting of cancer and functionally contributes to the impairment of antitumor immunity. However, its role during sepsis is unknown. Because patients with cancer are 10 times more likely to die of sepsis than previously healthy (PH) patients with sepsis, we interrogated the role of TIGIT during sepsis in the context of preexistent malignancy. PH mice or cancer (CA) mice inoculated with lung carcinoma cells were made septic by cecal ligation and puncture (CLP). We found that sepsis induced TIGIT upregulation predominantly on Tregs and NK cells in both PH and CA mice. Anti-TIGIT Ab improved the 7-d survival of CA septic mice but not PH mice after CLP. Treatment of CA septic animals but not PH septic animals with anti-TIGIT mAb significantly reversed sepsis-induced loss of CD4+ T cells, CD8+ T cells, Foxp3+ Treg, and CD19+ B cells in the spleen, which was the result of decreased caspase-3+ apoptotic cells. In sum, we found that anti-TIGIT Ab reversed sepsis-induced T cell apoptosis in CA septic mice and led to a significant survival benefit, suggesting its use as a potential immunotherapy to improve outcomes in septic patients with cancer.