Measurement of cytotoxic activity of NK/LAK cells

TL Whiteside - Current protocols in Immunology, 2000 - Wiley Online Library
TL Whiteside
Current protocols in Immunology, 2000Wiley Online Library
In this unit, methodology is presented for measuring the capacity of human natural killer (NK)
or lymphokine‐activated killer (LAK) cells to lyse tumor cell targets. Cytotoxicity of these
effector cells is evaluated in a short‐term 51Cr‐release assay using NK‐sensitive tumor
cells as the targets for NK cells or NK‐resistant tumor cells as the targets for LAK cells. In the
basic protocol, a generic 51Cr‐release assay is described in which PBMC, purified NK cells
or interleukin 2 (IL‐2)‐activated lymphocyte populations (LAK cells) are utilized as effector …
Abstract
In this unit, methodology is presented for measuring the capacity of human natural killer (NK) or lymphokine‐activated killer (LAK) cells to lyse tumor cell targets. Cytotoxicity of these effector cells is evaluated in a short‐term 51Cr‐release assay using NK‐sensitive tumor cells as the targets for NK cells or NK‐resistant tumor cells as the targets for LAK cells. In the basic protocol, a generic 51Cr‐release assay is described in which PBMC, purified NK cells or interleukin 2 (IL‐2)‐activated lymphocyte populations (LAK cells) are utilized as effector cells. Support protocols describe preparation of nonadherent tumor cells, cells obtained from malignant effusions, trypsinized tumor cells from adherent monolayer culture, or freshly isolated tumor cells from surgical specimens. All of these cell types can serve as the 51Cr‐labeled target cells in the basic protocol. The procedure for labeling target cells from any of these sources with 51Cr is also provided.
Wiley Online Library