Warren Hilary
Cancer Immunology Research Unit, The Canberra Hospital, Canberra, Australia.
Curr Protoc Immunol. 2012 Apr;Chapter 14:Unit 14.29.1-15. doi: 10.1002/0471142735.im1429s97.
Natural killer (NK) cells are an important effector cell of innate immunity. Their interaction with susceptible target cells triggers NK cell cytotoxicity and the release of cytokines. Immunofluorescence flow cytometry-based assays are now the preferred methods for measuring NK cell responses. For these assays, assessment is made on NK cells (CD3(-)CD56(+) CD16(+)) within the viable lymphocyte gate, defined by the parameters of size (FSC) and granularity (SSC). Accordingly, NK cells that have not dissociated from target cells at the time of measurement, or that have undergone target cell-induced apoptosis, are excluded from the viable lymphocyte gate and therefore from analysis. This unit describes a protocol for assessing NK cell function in response to target cells (both natural killing and antibody-dependent cell cytotoxicity) based on the loss of NK cells from the lymphocyte gate. This target-induced NK loss (TINKL) should provide a sensitive measure of NK cell responses in a clinical laboratory setting.
自然杀伤(NK)细胞是固有免疫的重要效应细胞。它们与易感靶细胞的相互作用会触发NK细胞的细胞毒性并释放细胞因子。基于免疫荧光流式细胞术的检测方法现在是测量NK细胞反应的首选方法。对于这些检测,需在由大小(FSC)和颗粒度(SSC)参数定义的活淋巴细胞门内对NK细胞(CD3(-)CD56(+)CD16(+))进行评估。因此,在测量时未与靶细胞解离或已发生靶细胞诱导凋亡的NK细胞会被排除在活淋巴细胞门外,从而也被排除在分析之外。本单元描述了一种基于淋巴细胞门内NK细胞的减少来评估NK细胞对靶细胞反应功能(包括自然杀伤和抗体依赖性细胞毒性)的方案。这种靶细胞诱导的NK细胞损失(TINKL)应能在临床实验室环境中为NK细胞反应提供一种灵敏的检测方法。
Curr Protoc Immunol. 2012-4
Curr Protoc Immunol. 2013
J Immunol Methods. 2011-6-15