TABLE 1.
Intracellular cytokine staining in lymph node cells from L. major-infected wild-type and TLR40/0 micea
Mouse strain | % CD4+ cells | % CD4+ IFN-γ+ cells | MFIb | % CD4+ IL-4+ cells | MFIb | % CD4+ IL-10+ cells | MFIb |
---|---|---|---|---|---|---|---|
Wild-type | 50.3 ± 2.0 | 6.1 ± 1.2 | 5.4 ± 0.2 | 1.3 ± 0.1 | 4.5 ± 0.2 | 2.3 ± 0.7 | 4.0 ± 0.2 |
TLR40/0 | 52.1 ± 2.8 | 7.7 ± 3.3 | 6.2 ± 1.5 | 1.9 ± 0.7 | 5.6 ± 1.0 | 2.8 ± 1.1 | 4.6 ± 0.2 |
Groups of wild-type and TLR40/0 mice were infected with 2 × 106 L. major promastigotes in one hind footpad. At 4 weeks postinfection, 5 × 106 popliteal lymph node cells were stimulated with 106 L. major parasites. Six days later, a Ficoll gradient was performed and the cells were restimulated with PMA and ionomycin in the presence of brefeldin-A, as described in Materials and Methods. The frequencies of IFN-γ-, IL-4-, and IL-10-expressing CD4+ T cells were determined by flow cytometry, and the values represent averages ± standard deviations for four mice. The results of one of two similar experiments are presented.
MFI, mean fluorescence intensity.