Fig. 5.
Fig. 5. Cytotoxic activity and phenotype of IL-2–activatedW/W NK cells. / (A) Spleen cells were depleted of red cells, B cells, and T cells, and the remaining cells were used to generate A-LAK cells. Day 7-10 A-LAK cells were used as effectors against YAC-1 cells (○) or EL-4 cells in the presence (▴) or absence of α-CD90 antibodies (•). All assays were done in duplicate or triplicate. (B) Day 7-10 A-LAK cells were stained with antibodies for CD3FITC, NK1.1PE, B220TRIC, and the expression of B220 on NK1.1+ CD3−NK cells was calculated. Data are representative of 3 independent experiments. Similar data were obtained with IL-15 (n = 2; data not shown).

Cytotoxic activity and phenotype of IL-2–activatedW/W NK cells.

(A) Spleen cells were depleted of red cells, B cells, and T cells, and the remaining cells were used to generate A-LAK cells. Day 7-10 A-LAK cells were used as effectors against YAC-1 cells (○) or EL-4 cells in the presence (▴) or absence of α-CD90 antibodies (•). All assays were done in duplicate or triplicate. (B) Day 7-10 A-LAK cells were stained with antibodies for CD3FITC, NK1.1PE, B220TRIC, and the expression of B220 on NK1.1+ CD3NK cells was calculated. Data are representative of 3 independent experiments. Similar data were obtained with IL-15 (n = 2; data not shown).

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