Table 3.
Cytokine Production after In Vivo Transfer of IRF-2+/− and IRF-2−/− CD4+ T Cells into RAG-1−/− Mice
Transferred cells | ||||||||
---|---|---|---|---|---|---|---|---|
– | IRF-2+/+ B cells | IRF-2+/+ B cells +IRF-2+/− CD4+ | IRF-2+/+ B cells +IRF-2−/− CD4+ | |||||
Parasite burden | 3.0 × 107 ± 2.7 × 107 | 7.2 × 106 ± 3.6 × 106 | 8.7 × 104 ± 1.3 × 104 | 4.0 × 104 ± 1.3 × 104 | ||||
In vitro stimulus | ||||||||
−LmAg | +LmAg | −LmAg | +LmAg | −LmAg | +LmAg | −LmAg | +LmAg | |
IFN-γ (pg/ml) | <40 | <40 | <40 | <40 | 80 ± 0 | 3,500 ± 70 | <40 | 2,000 ± 0 |
IL-4 (pg/ml) | <5 | <5 | <5 | <5 | 55 ± 35 | 375 ± 250 | <5 | 50 ± 14 |
6 wk after the start of the experiment, splenocytes were prepared from L. major–infected RAG-1−/− mice (three mice per group) as described in Materials and Methods. Parasite burden (expressed as the number of leishmania per spleen) and cytokine production in pooled cells from each group were determined as described in Materials and Methods. Data are shown as mean ± SD of triplicate determinations.