Table 1.
Peripheral CTL-mediated antiviral protection is short-lived in the absence of antigen
Challenge infection | Immunization* | Virus titer/organ (log10 ± SEM) in time of challenge infection after immunization
|
No. of surviving mice
|
||
---|---|---|---|---|---|
Day 10 | Day 60 | Day 10 | Day 60 | ||
LCMV i.f. | 3 × 106 GP2.9 | 2.0 ± 0.1 | 2.1 ± 0.3 | ||
1 × 105 GP2.9 | 2.1 ± 0.2 | 2.5 ± 0.1 | |||
3 × 106 MC57 | 3.8 ± 0.2 | 3.7 ± 0.1 | |||
vacc-GP i.p. | 3 × 106 GP2.9 | 1.1 ± 0.1 | 5.9 ± 0.3 | ||
1 × 105 GP2.9 | 4.0 ± 0.2 | 5.2 ± 0.1 | |||
3 × 106 MC57 | 6.1 ± 0.1 | 6.0 ± 0.1 | |||
LCMV i.c. | 3 × 106 GP2.9 | 6/6 | 2/6 | ||
3 × 106 MC57 | 0/6 | 0/6 |
Mice of the same groups as in Fig. 3 were challenged into the footpad (i.f.) with LCMV WE (30 pfu), and 7 days later virus titers were determined in the footpad (LCMV WE i.f.). Alternatively, mice were challenged i.p. with recombinant vaccinia virus expressing LCMV-GP, and virus titers were assessed 5 days later in ovaries (vacc-GP i.p.). Alternatively, mice primed with a high cell dose (6 per group) were challenged i.c. with LCMV WE (30 pfu), and survival was monitored (LCMV WE i.c.).