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. 2004 Apr;72(4):1920–1928. doi: 10.1128/IAI.72.4.1920-1928.2004

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
a

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.

b

MFI, mean fluorescence intensity.