Figure 1.
Figure 1. NIMA exposure reduces T-cell proliferative and cytokine responses to NIMAs. CD4+ T cells isolated from spleens of NIMA-exposed and control B6 mice were cultured with B6D2F1 DCs for 72 hours. Supernatants were collected for the measurement of IFN-γ levels, and the cells were pulsed with 3[H]thymidine to determine cell proliferation. Proliferation (A) and IFN-γ levels (B) are shown as mean ± SD. (C-D) A total of 5 × 105 CD4+ T cells isolated from spleens from NIMA-exposed and control mice were adoptively transferred into lethally irradiated B6D2F1 mice (C) or third-party B6C3F1 mice (D). Five days later, donor CD4+ T-cell expansion as determined by H-2d- CD4+ in MLNs was determined. *P < .05.

NIMA exposure reduces T-cell proliferative and cytokine responses to NIMAs. CD4+ T cells isolated from spleens of NIMA-exposed and control B6 mice were cultured with B6D2F1 DCs for 72 hours. Supernatants were collected for the measurement of IFN-γ levels, and the cells were pulsed with 3[H]thymidine to determine cell proliferation. Proliferation (A) and IFN-γ levels (B) are shown as mean ± SD. (C-D) A total of 5 × 105 CD4+ T cells isolated from spleens from NIMA-exposed and control mice were adoptively transferred into lethally irradiated B6D2F1 mice (C) or third-party B6C3F1 mice (D). Five days later, donor CD4+ T-cell expansion as determined by H-2d- CD4+ in MLNs was determined. *P < .05.

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