| Literature DB >> 29305140 |
Jihye Kim1, Dong-Yeop Chang2, Hyun Woong Lee3, Hoyoung Lee1, Jong Hoon Kim2, Pil Soo Sung2, Kyung Hwan Kim2, Seon-Hui Hong1, Wonseok Kang2, Jino Lee2, So Youn Shin2, Hee Tae Yu2, Sooseong You2, Yoon Seok Choi2, Insoo Oh2, Dong Ho Lee4, Dong Hyeon Lee5, Min Kyung Jung2, Kyung-Suk Suh6, Shin Hwang7, Won Kim5, Su-Hyung Park8, Hyung Joon Kim9, Eui-Cheol Shin10.
Abstract
Acute hepatitis A (AHA) involves severe CD8+ T cell-mediated liver injury. Here we showed during AHA, CD8+ T cells specific to unrelated viruses became activated. Hepatitis A virus (HAV)-infected cells produced IL-15 that induced T cell receptor (TCR)-independent activation of memory CD8+ T cells. TCR-independent activation of non-HAV-specific CD8+ T cells were detected in patients, as indicated by NKG2D upregulation, a marker of TCR-independent T cell activation by IL-15. CD8+ T cells derived from AHA patients exerted innate-like cytotoxicity triggered by activating receptors NKG2D and NKp30 without TCR engagement. We demonstrated that the severity of liver injury in AHA patients correlated with the activation of HAV-unrelated virus-specific CD8+ T cells and the innate-like cytolytic activity of CD8+ T cells, but not the activation of HAV-specific T cells. Thus, host injury in AHA is associated with innate-like cytotoxicity of bystander-activated CD8+ T cells, a result with implications for acute viral diseases.Entities:
Keywords: CD8(+) T cells; IL-15; NKG2D; bystander activation; host injury; immunopathogenesis; viral hepatitis; virus
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Year: 2018 PMID: 29305140 DOI: 10.1016/j.immuni.2017.11.025
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745