Fig. 3.
Fig. 3. Impaired allostimulatory activity of FL DCs in MLR. / (A) Five thousand irradiated DCs isolated from B6D2F1 mice were cultured with 105 T cells from either B6 (allogeneic) or B6D2F1 (syngeneic) mice as described in “Materials and methods.” T-cell proliferation was determined by 3H-thymidine incorporation. Allogeneic T-cell responses to control DCs (open circle) and to FL DCs (closed circle) and syngeneic T-cell responses to control DCs (open square) and to FL DCs (closed square) are shown. Data are the mean ± SD of quadruplicate cultures. (B, C) Supernatants of cultures with control DCs (open bar) or with FL DCs (closed bar) were collected at 24 hours for IL-2 (B) and at 72 hours for IFN-γ (C) and measured by ELISA as described in “Materials and methods.”

Impaired allostimulatory activity of FL DCs in MLR.

(A) Five thousand irradiated DCs isolated from B6D2F1 mice were cultured with 105 T cells from either B6 (allogeneic) or B6D2F1 (syngeneic) mice as described in “Materials and methods.” T-cell proliferation was determined by 3H-thymidine incorporation. Allogeneic T-cell responses to control DCs (open circle) and to FL DCs (closed circle) and syngeneic T-cell responses to control DCs (open square) and to FL DCs (closed square) are shown. Data are the mean ± SD of quadruplicate cultures. (B, C) Supernatants of cultures with control DCs (open bar) or with FL DCs (closed bar) were collected at 24 hours for IL-2 (B) and at 72 hours for IFN-γ (C) and measured by ELISA as described in “Materials and methods.”

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