In chronic hepatitis B virus (HBV)-infected patients, T helper 17 (Th17) cells are significantly elevated. Th17 cells initiate immune‑mediated pathogenesis and have a critical role in the process of HBV‑related liver cirrhosis (HBV‑LC). The mechanisms underlying this process are attributed to Th17‑secreted cytokines, which include interleukin (IL)‑17, IL‑21 and IL‑22; however, a systemic analysis regarding these mechanisms has yet to be conducted. Therefore, the present study aimed to investigate the role of Th17 cells in the pathogenesis of HBV‑LC. All randomized clinical trials, case series, case reports and meta‑analyses that contained the aforementioned keywords were included in the review process. In addition, unpublished information from the Food and Drug Administration was included. The findings indicated that Th17‑secreted cytokines, including IL‑17, IL‑21 and IL‑22, function by activating or silencing hepatic stellate cells, modulating proinflammatory and pro‑ or antifibrogenic effectors, regulating extracellular matrix formation, upregulating chemokine expression, and inducing hepatocellular damage or hepatoprotection during the HBV‑LC process. In addition, Th17 cells and Th17‑secreted cytokines may be considered a potential tool in the diagnosis or treatment of HBV‑LC. The present review summarized the role of Th17 cells in the pathogenesis of HBV‑LC in order to deepen the clinical understanding of the role of Th17 cells and also to support the development of effective therapies for patients with HBV‑LC.

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