Mice infected with sessile opaque pneumococci had bacteria in the lungs, whereas not detectable number of pneumococci could be recovered from mice infected with other phenotypic variants (P = 0.0002).
In contrast to vehicle treated animals, almost no MOG35 55-specific MOG35 55-specificoducing CD4+ cells could be recovered from mice treated with orX 0914.
Similar CFU counts of the WT, YHΔtpx and YHtpxComp were recovered from mouse lungs and spleens after 4 hours of infection (CFU counts: WT, 5.88 logCFU/lung and 6.02 logCFU/spleen. YHΔtpX, 5.87 logCFU/lung and 6.01 logCFU/spleen. YHtpXComp, 5.87 logCFU/lung and 5.99 logCFU/spleen).
Eggs were recovered from mouse livers infected 7 weeks prior with cercariae as previously described [ 64].
These similarities likely reflect adaptations to the aquatic environment and parasitism of the snail host, but are somewhat surprising in regards to the eggs, given that these were recovered from mouse livers.
Study Design: TDLNs were recovered from mice bearing progressive MCA 205 fibrosarcomas, and the T lymphocytes were segregated into CD62Llow and CD62Lhigh subsets and activated ex vivo with anti-CD3 mAb and IL-2.
In contrast, significantly lower bacterial counts were recovered from mice immunized with IC31®-adjuvanted Ag85B-ESAT-6 either as adults or as neonates (Figure 6A, B).
In contrast, significantly lower bacterial counts were recovered from mice immunized with Ag85B-ESAT-6 in CAF01 either as adults or as neonates (Figure 1).
Plasma was recovered from mice in group A C in which the animals were sacrificed on day 16, and after sonication re-injected into new recipient mice (groups D F, respectively).
Significantly fewer bacteria were recovered from mice in the AbHV2BD linear test group compared to mice for which AbHV2A linear was used as a negative control (p≤0.03) on days 1 and 2 post-inoculation.
