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. 2010 Dec;162(3):447–459. doi: 10.1111/j.1365-2249.2010.04274.x

Table 6.

Functional responses of natural killer (NK) T cell lines

Experiment 1 Patient B2 Patient B7
Autologous tumour + αGalCer 0 0
Autologous tumour 1 1
Autologous tumour lysate + C1R-huCD1d§ + αGalCer n.t. 3
Autologous tumour lysate + C1R-huCD1d n.t. 2
Controls
 C1R-huCD1d + αGalCer 26 15
 C1R-huCD1d 2 7
 C1R + αGalCer 1 0
 C1R 1 0
 PMA/ionomycin 11 (61) 14 (54)
 Medium 0 0
Experiment 2 Patient B2 Patient B7
Autologous tumour + αGalCer 0 7
Autologous tumour 0 0
Autologous tumour lysate + C1R-huCD1d + αGalCer 5 1
Autologous tumour lysate + C1R-huCD1d 1 0
allogeneic tumour lysate†† + C1R-huCD1d + αGalCer 5 1
allogeneic tumour lysate + C1R-huCD1d 1 0
Controls
 C1R-huCD1d + αGalCer 7 8
 C1R-huCD1d 4 0
 C1R + αGalCer 0 0
 C1R 0 0
 PMA/ionomycin 22 (36) 22 (23)
 Medium 0 0

α-Galactosylceramide (αGalCer).

Interferon (IFN)-γ spots/well of 5 × 102 effector cells co-cultured overnight with 2 × 103 targets in enzyme-linked immunospot assay.

§

C1R cell line untransfected (C1R) or transfected with human CD1d (C1R-huCD1d).

Within brackets, responses of allogeneic peripheral blood mononuclear cell effectors.

††

Lysates of the other NK T patient were used.

PMA: phorbol myristate acetate; n.t.: not tested.