Treatment options for chronic hepatitis B (CHB) infection are extremely limited. CXCR5(+) CD8(+) T cell is a novel cell subtype and could possess strong cytotoxic properties in HIV infection. In this study, we investigated the role of CXCR5(+) CD8(+) T cells in CHB patients. Compared to healthy individuals, both CHB patients and hepatitis B virus (HBV)-infected hepatocellular carcinoma patients presented significant upregulation of CXCR5(+) CD8(+) T cells in peripheral blood, in which CXCR5(+) CD8(+) T cells were negatively correlated with the frequency of CXCR5(+) CD4(+) T cells in CHB patients. After PMA+ ionomycin stimulation, CXCR5(+) CD8(+) T cells from CHB patients presented significantly higher transcription level of interferon gamma (IFN-gamma), interleukin 10 (IL-10), and IL-21, as well as higher IL-10 and IL-21 protein secretion, than CXCR5-CD8(+) T cells. Unlike CXCR5(+) CD4(+) T cells, when incubated with naive CD19(+) CD27-B cells, CXCR5(+) CD8(+) T cells alone did not upregulate IgM, IgG, and IgA secretion. However, addition of CXCR5(+) CD8(+) T cells in B cell-CXCR5(+) CD4(+) T cell coculture significantly increased the levels of secreted IgG and IgA, demonstrating that CXCR5(+) CD8(+) T cell could indirectly offer B cell help. Furthermore, high frequencies of CXCR5(+) CD8(+) T cells tended to associate with low HBV DNA load, and the frequency of CXCR5(+) CD8(+) T cells was negatively correlated with alanine aminotransferase (ALT) level. Together, these results suggested that CXCR5(+) CD8(+) T cells were involved in the antiviral immune responses in CHB and could potentially serve as a therapeutic candidate.