| Literature DB >> 24944796 |
Baskar Subramani1, Chithra Ramanathan Pullai1, Kohila Krishnan1, Sheela Devi Sugadan1, Xuewen Deng2, Terunuma Hiroshi3, Kananathan Ratnavelu3.
Abstract
Immune cell-based therapies using natural killer (NK) cells and cytotoxic T cells are under constant scrutiny, with the aim to design an effective and reduced-toxicity therapy, which will benefit patients via improved quality of life and improved prognosis. Four patients with stage IV colon cancer were administered 1, 3, 5 and 6 effector cell intravenous infusions, respectively. Peripheral blood was collected from the patients and the ex vivo activation and expansion of NK and T cells was performed in Good Manufacturing Practice-certified clean rooms for ~12-15 days. Immunophenotypic analysis of the peripheral blood mononuclear cells (PBMCs) and expanded NK and T cells was conducted using flow cytometry and the patients were followed up. On average, 4.8×107 initial PBMCs and 2.7×109 total expanded cells were obtained. The intravenous infusions of the expanded cells were not accompanied by adverse reactions. Improved prognosis, reflected by a considerable decrease in the cancer markers, accompanied by an improved quality of life in the patients were observed. In conclusion, potential strategies are currently under development for the large-scale production of effectors cells; therefore, autologous immune enhancement therapy (AIET) may be considered as a viable approach to cancer treatment.Entities:
Keywords: FOLFOX; autologous immune enhancement therapy; colorectal cancer
Year: 2014 PMID: 24944796 PMCID: PMC4051481 DOI: 10.3892/br.2014.264
Source DB: PubMed Journal: Biomed Rep ISSN: 2049-9434