Overrepresentation of IL-10-Expressing B Cells Suppresses Cytotoxic CD4(+) T Cell Activity in HBV-Induced Hepatocellular Carcinoma

Hepatocellular carcinoma (HCC) is a common cancer with poor prognosis and low five-year survival rate. A strong and effective CD4(+) T cell-mediated cytotoxicity was associated with better survival and low recurrence rate in HCC, but the regulatory mechanism that controls CD4(+) T cell cytotoxicity in HCC patients is not fully examined. Given that IL-10-expressing B cells could suppress the inflammation of cytotoxic CD8(+) T cells, T helper 1 (Th1) cells and Th17 cells, while promoting regulatory T (Treg) cell differentiation, we examined the role of IL-10-expressing B cells in HBV-related HCC patients. We found that compared to healthy controls, HCC patients exhibited significantly higher frequencies of IL-10-expressing B cells, which were negatively correlated with the frequencies of granzyme A, granzyme B, and perforin expressing CD4(+) T cells. Surface molecule Tim-1 was preferentially expressed on IL-10-expressing B cells. Therefore, we separated total B cells into Tim-1(+) and Tim-1(-) B cells. CD4(+) T cells incubated with Tim-1(+) B cells exhibited significantly reduced levels of granzyme A, granzyme B and perforin expression, compared to the CD4(+) T cells incubated with Tim-1(-) B cells. Antagonizing IL-10 in culture rescued CD4(+) T cell cytotoxicity. Compared to that in peripheral blood, the level of IL-10-expressing B cells were further upregulated in resected tumor, while the level of CD4(+) cytotoxic T cells was downregulated. The negative correlations between IL-10-expressing B cells and CD4(+) cytotoxic T cells were also observed in tumor-infiltrating cells. Together, our data revealed an additional antitumor mechanism mediated by IL-10-expressing B cells.