Table 3. Induction of IgA CSR on B-1 B cells co-cultured with DCs plus cytokinesa.
Nasal Immunization with | DCs from (4×105 cells/ml) | % of IgA+ cells on B-1 B cells | ||
IL-5 (100 ng/ml) | TGF-β1 (1 ng/ml) | IL-5 (100 ng/ml)+TGF-β1 (1 ng/ml) | ||
nCT | SMGs | 0.5±0.2 | 0.2±0.2 | 0.8±0.3 |
NPs | 0.4±0.2 | 0.2±0.3 | 0.7±0.2 | |
CLNs | 0.2±0.3 | 0.0±0.2 | 0.5±0.2 | |
TNP-LPS | SMGs | 0.4±0.4 | 0.2±0.8 | 1.9±0.8 |
NPs | 0.3±0.2 | 0.3±0.2 | 1.2±0.4 | |
CLNs | 0.4±0.5 | 0.2±2.6 | 0.9±0.3 | |
TNP-LPS + nCT | SMGs | 0.5±0.1 | 0.3±0.1 | * , #4.8±0.5 |
NPs | 0.4±0.2 | 0.4±0.2 | * , #2.7±0.7 | |
CLNs | 0.4±0.3 | 0.4±0.1 | * , #2.4±0.7 |
IgA negative B cells from SMGs, NPs and CLNs from the peritoneal cavity cells were co-cultured with DCs plus IL-5, TGF-β1, or both IL-5 and TGF-β1 for five days, and were stained with FITC-conjugated anti-IgA mAb and were then subjected to flow cytometry analysis by FACSCalibur®.
*p<0.05 compared with immunized mice given TNP-LPS alone.
p<0.05 compared with immunized mice given nCT alone.