Figure 4.
Figure 4. Effect of adoptively transferred Aspergillus-pulsed DCs on the induction of antifungal TH immunity. Splenic DCs were pulsed and administered into mice subsequently infected intravenously with A fumigatus or C albicans as described in Figure 3. Antifungal TH immunity was assessed in terms of cytokine production (ELISA) by antigen-stimulated CD4+ T splenocytes from mice with aspergillosis (A) or candidiasis (B) or cytokine gene expression by real-time PCR (C). ELISA and real-time PCR were done 6 days after the infection. *P < .05 (mice receiving pulsed DCs versus mice receiving unpulsed DCs). ▪, unpulsed DCs; ▨, conidia-pulsed DCs; ▦, conidial RNA-transfected DCs. Error bars indicate SE.

Effect of adoptively transferredAspergillus-pulsed DCs on the induction of antifungal THimmunity. Splenic DCs were pulsed and administered into mice subsequently infected intravenously with A fumigatus or C albicans as described in Figure 3. Antifungal TH immunity was assessed in terms of cytokine production (ELISA) by antigen-stimulated CD4+ T splenocytes from mice with aspergillosis (A) or candidiasis (B) or cytokine gene expression by real-time PCR (C). ELISA and real-time PCR were done 6 days after the infection. *P < .05 (mice receiving pulsed DCs versus mice receiving unpulsed DCs). ▪, unpulsed DCs; ▨, conidia-pulsed DCs; ▦, conidial RNA-transfected DCs. Error bars indicate SE.

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