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受乙肝相关肝硬化影响的人类肝脏中免疫细胞的单细胞图谱

Single-cell landscape of immune cells in human livers affected by HBV-related cirrhosis.

作者信息

Bai Qingquan, Hong Xiaoting, Lin Han, He Xiao, Li Runyang, Hassan Mohsin, Berger Hilmar, Tacke Frank, Engelmann Cornelius, Hu Tianhui

机构信息

Cancer Research Center, School of Medicine, Xiamen University, Xiamen, China.

National Institute for Data Science in Health and Medicine, Xiamen University, Xiamen, China.

出版信息

JHEP Rep. 2023 Aug 18;5(11):100883. doi: 10.1016/j.jhepr.2023.100883. eCollection 2023 Nov.

Abstract

BACKGROUND & AIMS: HBV infection is one of the leading causes of liver cirrhosis. However, the immune microenvironment in patients with HBV cirrhosis remains elusive.

METHODS

Single-cell RNA sequencing was used to analyse the transcriptomes of 76,210 immune cells in the livers of six healthy individuals and in five patients with HBV cirrhosis.

RESULTS

Patients with HBV cirrhosis have a unique immune ecosystem characterised by an accumulation of macrophage-CD9/IL18, macrophage-C1QA, NK Cell-JUNB, CD4 T cell-IL7R, and a loss of B cell-IGLC1 clusters. Furthermore, our analysis predicted enhanced cell communication between myeloid cells and all immune cells in patients with HBV-related cirrhosis. Pseudo-time analysis of myeloid cells, natural killer (NK) cells, and B cells demonstrated a significant accumulation of mature cells and a depletion of naive cells in HBV cirrhosis. In addition, we observed an increase in antigen processing and presentation capacities in myeloid cells in patients with HBV cirrhosis, whereas NK cell-mediated cytotoxicity was substantially reduced.

CONCLUSIONS

Our results provide valuable insight into the immune landscape of HBV cirrhosis, suggesting that HBV cirrhosis is associated with the accumulation of activated myeloid cells and impaired cytotoxicity in NK cells.

IMPACT AND IMPLICATIONS

The absence of single-cell transcriptome profiling of immune cells in HBV cirrhosis hinders our understanding of the underlying mechanisms driving disease progression. To address this knowledge gap, our study unveils a distinctive immune ecosystem in HBV cirrhosis and represents a crucial advancement in elucidating the impact of the immune milieu on the development of this condition. These findings constitute significant strides towards the identification of more effective therapeutic approaches for HBV cirrhosis and are relevant for healthcare professionals, researchers, and pharmaceutical developers dedicated to combating this disease.

摘要

背景与目的

乙肝病毒(HBV)感染是肝硬化的主要病因之一。然而,HBV肝硬化患者的免疫微环境仍不清楚。

方法

采用单细胞RNA测序分析6名健康个体和5名HBV肝硬化患者肝脏中76210个免疫细胞的转录组。

结果

HBV肝硬化患者具有独特的免疫生态系统,其特征为巨噬细胞-CD9/白细胞介素18、巨噬细胞-C1QA、自然杀伤(NK)细胞-JUNB、CD4 T细胞-白细胞介素7受体聚集,以及B细胞-免疫球蛋白轻链C1簇缺失。此外,我们的分析预测HBV相关性肝硬化患者骨髓细胞与所有免疫细胞之间的细胞通讯增强。对骨髓细胞、NK细胞和B细胞进行的伪时间分析表明,HBV肝硬化中成熟细胞显著聚集,幼稚细胞减少。此外,我们观察到HBV肝硬化患者骨髓细胞的抗原加工和呈递能力增加,而NK细胞介导的细胞毒性显著降低。

结论

我们的结果为HBV肝硬化的免疫格局提供了有价值的见解,表明HBV肝硬化与活化骨髓细胞的积累和NK细胞细胞毒性受损有关。

影响与意义

缺乏对HBV肝硬化免疫细胞的单细胞转录组分析阻碍了我们对驱动疾病进展的潜在机制的理解。为了填补这一知识空白,我们的研究揭示了HBV肝硬化中独特的免疫生态系统,代表了在阐明免疫环境对这种疾病发展的影响方面的关键进展。这些发现为确定更有效的HBV肝硬化治疗方法迈出了重要一步,对致力于对抗这种疾病的医疗专业人员、研究人员和药物开发商具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2bc/10582775/400c64c69d14/ga1.jpg

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