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Autologous cytokine-induced killer (CIK) cells are an ex vivo expanded population of immune effector cells, characterized by a dual T-cell and natural killer (NK) cell phenotype (predominantly CD3+CD56+). Developed by Chuan An Biotechnology for the treatment of hepatocellular carcinoma (HCC), these cells are generated by culturing a patient's peripheral blood mononuclear cells with interferon-gamma, anti-CD3 antibodies, and interleukin-2. CIK cells exhibit potent, non-major histocompatibility complex (MHC)-restricted cytotoxic activity against tumor cells, primarily mediated through the NKG2D receptor. In clinical applications, they are often used as an adjuvant therapy following local treatments such as transarterial chemoembolization (TACE), percutaneous ethanol injection therapy (PEIT), or radiofrequency ablation (RFA) to target residual disease and reduce the risk of recurrence.
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