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Autologous cytokine-induced killer (CIK) cells are an ex vivo expanded population of immune effector cells, primarily T lymphocytes, used as a form of adoptive cell immunotherapy. These cells are generated from a patient's own peripheral blood mononuclear cells (PBMCs) through a standardized culture process involving stimulation with interferon-gamma (IFN-γ), interleukin-2 (IL-2), and anti-CD3 monoclonal antibodies. CIK cells are characterized by a CD3+CD56+ phenotype and possess potent, non-MHC-restricted cytolytic activity against a broad range of tumor cells, primarily mediated by the NKG2D receptor. The People's Hospital of Guangxi Zhuang Autonomous Region has evaluated these cells as a maintenance immunotherapy for patients with advanced (Stage IIIb/IV) nonsquamous non-small cell lung cancer (NSCLC) to prolong progression-free survival and improve quality of life following initial chemotherapy.
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