Percutaneous ablation therapy has been widely accepted as one of the radical treatment methods for small hepatocellular carcinoma (HCC) and the 5-year survival rate is similar to that obtained by resection. 1 The search for new and effective methods to prolong the overall survival and disease-free survival time requires further advances. HCC is a potential target for immunotherapy, as evidenced by an active recruitment of tumor-infiltrating lymphocytes (TIL) that display antitumor cytolytic activity in the presence of interleukin (IL) 2 in ex vivo studies.2 However, TIL in HCC are of dysfunction, few in quantity and do not kill tumor cells, which suggests that immunosuppressive mechanisms prevent T cells from maturing into effective antitumor effectors. The activation of tumor-specific cytotoxic T lymphocytes (CTL) requires three synergistic signals: the presentation of tumor antigen by antigen-presenting cells (APC) to specific T-helper cells; the interaction between costimulatory factors (such as B7.1 and CD28 ligand); Background and Aims: To observe safety and influence on viral load and peripheral T-lymphocyte subsets of combination therapy with percutaneous microwave ablation (PMWa) and adoptive immunotherapy in hepatocellular carcinoma (HCC) with hepatitis B.Results: no adverse effects of grade iii/iV were observed. Viral load was decreased in 57.14% (four of seven) of patients and was undetectable in two (28.6%) patients without antiviral therapy. The percentage of Cd4 + Cd25 high regulatory T lymphocytes decreased significantly and the percentage of Cd8 + Cd28 -effector cells increased significantly 1 month after therapy. However, 6 months after therapy, there was no significant difference.Methods: Ten HCC (d ≤5 cm, fewer than three tumors) patients were treated with radical PMWa and three courses of immunotherapy, which were started with PMWa, 2 weeks post-PMWa and 3 months after PMWa. Peripheral blood mononuclear cells were differentiated into phenotypically confirmed dCs and effector cells. immature dCs, cytokineinduced killer cells (CiK) and cytotoxic T lymphocytes (CTL) were injected into the marginal area of ablated tumors under contrast-enhanced sonographic guidance. under sonographic guidance, tumor lysate-pulsed dC was injected into groin lymph nodes, while dC-CiK and CTL were injected into the abdominal cavity. CiK was infused intravenously.Conclusion: adoptive immunotherapy prescribed soon after PMWa for HCC patients was safe and ameliorated the percentage of peripheral lymphocytes.