Figure 2
Memory B cells protect from MCMV dissemination in the absence of a functional NK-cell response. (A) MCMV titers and (B) viral DNA copies in lung, spleen, and salivary gland 21 days after infection with 105 pfu MCMV157luc. Results from RAG−/− mice adoptively transferred with 5 × 106 B cells from MCMV-infected mice (•) or with 5 × 106 naive B cells (○) are shown (median values of 5 mice/group are indicated as lines). In all recipient animals, CD4+ and CD8+ T cells were depleted 2 days after transfer by application of the appropriate monoclonal antibodies to exclude contribution of T cells to reduction in viral load. There were significantly reduced virus titers in lung and salivary gland in the memory B-cell group (P < .01) and significantly reduced viral DNA copies in all organs (P < .01 for lung and salivary gland, P < .05 for spleen).

Memory B cells protect from MCMV dissemination in the absence of a functional NK-cell response. (A) MCMV titers and (B) viral DNA copies in lung, spleen, and salivary gland 21 days after infection with 105 pfu MCMV157luc. Results from RAG−/− mice adoptively transferred with 5 × 106 B cells from MCMV-infected mice (•) or with 5 × 106 naive B cells (○) are shown (median values of 5 mice/group are indicated as lines). In all recipient animals, CD4+ and CD8+ T cells were depleted 2 days after transfer by application of the appropriate monoclonal antibodies to exclude contribution of T cells to reduction in viral load. There were significantly reduced virus titers in lung and salivary gland in the memory B-cell group (P < .01) and significantly reduced viral DNA copies in all organs (P < .01 for lung and salivary gland, P < .05 for spleen).

Close Modal

or Create an Account

Close Modal
Close Modal