Hepatocellular carcinoma (HCC) has a high morbidity and mortality rate worldwide, with limited treatment options. Glypican-3 (GPC3) is a glycosylphosphatidylinositol-anchored glycoprotein that is overexpressed in most HCC tissues but not in normal tissues. GPC3-targeting antibody therapy shows limited response in a clinical trial due to the lack of a tumor-specific cytotoxic T lymphocyte (CTL) response. Here, in C57/B6 mice, we demonstrated that intravenous infusion of GPC3-coupled lymphocytes (LC/GPC3) elicited robust GPC3-specific antibody and CTL responses, which effectively restricted proliferation and lysed cultured-HCC cells. Treatment with LC/GPC3 induced durable tumor regression in HCC-bearing C57/B6 mice. Administration of LC/GPC3 induced elevated levels of the cytotoxic T cell bioactive factors tumor necrosis factor alpha (TNF-α), interferon-γ (IFN-γ), granzyme B, and perforin, and substantially increased the number of infiltrating CD8 T cells in tumor tissues. Moreover, immune responses elicited by LC/GPC3 selectively suppressed GPC3 tumors, but didn't affect the GPC3 tumors in BALB/c mice. Our findings provide the first preclinical evidence that intravenous infusion of the LC/GPC3 complex can induce a strong anti-HCC effect through regulating systemic and local immune responses. These results indicate that the LC/GPC3 complex could be developed as precision therapeutics for HCC patients in the future.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5628867 | PMC |
http://dx.doi.org/10.1016/j.ymthe.2017.08.005 | DOI Listing |
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