In “immunological checkups”, the resistance power against carcinogenesis or infection is investigated based on the cytotoxic activity and sub-classification of cells responsible for immunity. In addition, the immunity-activating effects of treatment with immunity-enhancing agents, Sino-Japanese medicines, or an agaricus blazei extract in vitro are determined to enhance the immune capacity and promote health.
Resting venous blood was aseptically collected, and peripheral blood mononuclear cells (PBMC) were collected by specific gravity centrifugation. After anaerobic culture of untreated PBMC (effector cells) and 7 kinds of PBMC treated with an agent or an extract for 24 hours, the effector cells and NK-sensitive K562 cells (chronic myelocytic leukemia cells) were assayed for 4 hours to graph the cytotoxic effects on the target cells, K562 cells.
Furthermore, staining with a monoclonal antibody was performed, and the 7 kinds (9items) of PBMC were measured and analyzed. In addition to the sub-classification of PBMC, the ratio of NK cells in effector cells was calculated, facilitating qualitative analysis of cytotoxic activity. To manage the accuracy, specimens were stored at room temperature, and isolated/treated within 5 hours after blood collection. We used K562 cells that had been cultured by cell passage at approximately 5 × 10
8 cells/ml 3 days or more after fusion.
Thorough accuracy management and data analysis facilitate examination at the cellular level. In the future, this procedure may be useful in many fields such as prophylactic medicine, evaluation of the response to immunotherapy, and studies on the immune capacity.
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