From the, Division of Gastroenterology, (IdM, IgM, BS, VK), Department of Medicine, University of California San Diego, La Jolla, California.
Gastroenterology Section, (TRM), VA Long Beach Healthcare System, Long Beach, California.
Alcohol Clin Exp Res. 2020 May;44(5):1061-1074. doi: 10.1111/acer.14323. Epub 2020 Apr 10.
Liver is enriched in several innate-like unconventional T cells, but their role in alcohol-related liver disease (ALD) is not fully understood. Studies in several acute alcohol feeding models but not in chronic alcoholic steatohepatitis (ASH) model have shown that invariant natural killer T (iNKT) cells play a pathogenic role in ALD. Here, we investigated the activation of iNKT cells in an intragastric (iG) infusion model of chronic ASH as well as the frequency and cytokine phenotype of 3 different unconventional T cells: iNKT, mucosal-associated invariant T (MAIT), and CD8 CD161 Vα7.2 cells in peripheral blood of ALD patients.
Hepatic iNKT cells were investigated using the iG model of chronic ASH that combines feeding of high-cholesterol/high-fat diet (HCFD) with intragastric feeding of ethanol diet (HCFD + iG Alc). Human iNKT, MAIT, and CD8 CD161 Vα7.2 cells were examined by flow cytometry in peripheral blood of patients with severe alcoholic hepatitis (SAH) and chronic alcoholics (ChA) and compared with healthy controls.
In the iG model of chronic ASH, IFNγ iNKT cells accumulate in their livers compared with pair-fed control mice and activated hepatic iNKT cells show high expression of Fas and FasL. Notably, IFNγ iNKT cells are also significantly increased in peripheral blood of ChA patients compared with SAH patients. MAIT cells are significantly reduced in all ALD patients, but CD8 CD161 Vα7.2 cells are increased in SAH patients. Although MAIT and CD8 CD161 Vα7.2 cells displayed a similar cytokine production profile, the production of IFNγ and TNFα is significantly increased in SAH patients, while significant IL-17A production is found in ChA patients.
We found that the 3 unconventional T cells are activated in ALD patients showing interesting differences in their frequency and cytokine production profile between SAH and ChA patients. In the iG murine model of chronic ASH, iNKT cells are also activated secreting proinflammatory cytokines suggesting their involvement in liver disease.
肝脏富含几种固有样非传统 T 细胞,但它们在酒精相关肝病 (ALD) 中的作用尚未完全阐明。在几种急性酒精喂养模型中,但不是在慢性酒精性脂肪性肝炎 (ASH) 模型中,研究表明不变自然杀伤 T (iNKT) 细胞在 ALD 中发挥致病作用。在这里,我们研究了胃内 (iG) 输注慢性 ASH 模型中 iNKT 细胞的激活,以及外周血中 3 种不同非传统 T 细胞(iNKT、黏膜相关不变 T (MAIT) 和 CD8 CD161 Vα7.2 细胞)的频率和细胞因子表型在 ALD 患者中。
使用结合高胆固醇/高脂肪饮食 (HCFD) 与胃内乙醇饮食喂养 (HCFD+iG Alc) 的慢性 ASH iG 模型研究肝内 iNKT 细胞。通过流式细胞术检查严重酒精性肝炎 (SAH) 和慢性酒精中毒 (ChA) 患者外周血中的人类 iNKT、MAIT 和 CD8 CD161 Vα7.2 细胞,并与健康对照进行比较。
在慢性 ASH 的 iG 模型中,与配对喂养的对照小鼠相比,IFNγ iNKT 细胞在肝脏中积聚,并且活化的肝内 iNKT 细胞表现出 Fas 和 FasL 的高表达。值得注意的是,ChA 患者外周血中的 IFNγ iNKT 细胞也显著增加。所有 ALD 患者的 MAIT 细胞均显著减少,但 SAH 患者的 CD8 CD161 Vα7.2 细胞增加。尽管 MAIT 和 CD8 CD161 Vα7.2 细胞显示出相似的细胞因子产生谱,但 SAH 患者的 IFNγ 和 TNFα 产生显著增加,而 ChA 患者则发现显著的 IL-17A 产生。
我们发现,在 ALD 患者中,3 种非传统 T 细胞被激活,SAH 和 ChA 患者之间其频率和细胞因子产生谱存在有趣的差异。在慢性 ASH 的 iG 小鼠模型中,iNKT 细胞也被激活,分泌促炎细胞因子,提示其参与肝病。