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Evaluation of peripheral blood T-lymphocyte subpopulations features in patients with hepatitis B virus-related acute-on-chronic liver failure based on single-cell sequencing technology / 中华肝脏病杂志
Chinese Journal of Hepatology ; (12): 422-427, 2023.
Article in Chinese | WPRIM | ID: wpr-986146
ABSTRACT

Objective:

T lymphocyte exhaustion is an important component of immune dysfunction. Therefore, exploring peripheral blood-exhausted T lymphocyte features in patients with hepatitis B virus-related acute-on-chronic liver failure may provide potential therapeutic target molecules for ACLF immune dysfunction.

Methods:

Six cases with HBV-ACLF and three healthy controls were selected for T-cell heterogeneity detection using the single-cell RNA sequencing method. In addition, exhausted T lymphocyte subpopulations were screened to analyze their gene expression features, and their developmental trajectories quasi-timing. An independent sample t-test was used to compare the samples between the two groups.

Results:

Peripheral blood T lymphocytes in HBV-ACLF patients had different differentiation trajectories with different features distinct into eight subpopulations. Among them, the CD4(+)TIGIT(+) subsets (P = 0.007) and CD8(+)LAG3(+) (P = 0.010) subsets with highly exhausted genes were significantly higher than those in healthy controls. Quasi-time analysis showed that CD4(+)TIGIT(+) and CD8(+)LAG3(+) subsets appeared in the late stage of T lymphocyte differentiation, suggesting the transition of T lymphocyte from naïve-effector-exhausted during ACLF pathogenesis.

Conclusion:

There is heterogeneity in peripheral blood T lymphocyte differentiation in patients with HBV-ACLF, and the number of exhausted T cells featured by CD4(+)TIGIT(+)T cell and CD8(+)LAG3(+) T cell subsets increases significantly, suggesting that T lymphocyte immune exhaustion is involved in the immune dysfunction of HBV-ACLF, thereby identifying potential effective target molecules for improving ACLF patients' immune function.
Subject(s)

Full text: Available Index: WPRIM (Western Pacific) Main subject: Receptors, Immunologic / Hepatitis B virus / T-Lymphocyte Subsets / Hepatitis B, Chronic / Acute-On-Chronic Liver Failure Limits: Humans Language: Chinese Journal: Chinese Journal of Hepatology Year: 2023 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Receptors, Immunologic / Hepatitis B virus / T-Lymphocyte Subsets / Hepatitis B, Chronic / Acute-On-Chronic Liver Failure Limits: Humans Language: Chinese Journal: Chinese Journal of Hepatology Year: 2023 Type: Article