TABLE 1.
Mouse | Virus | Total no. of cells per thymus samplea | Mean % of total thymocytes ± SE
|
No. of leukocytes/μl | % Lymphocytes in peripheral bloodc | ||
---|---|---|---|---|---|---|---|
CD4+ CD8+ | CD4+ CD8− | CD4− CD8+ | |||||
B6/129 | None | 1.02 × 108 | 89.0 ± 0.6 | 6.5 ± 0.9 | 2.0 ± 0.1 | 7.0 × 103 | 66.2 |
B6/129 | HK/483 | 1.26 × 107b | 42.5 ± 13.7b | 32.0 ± 9.8 | 14.8 ± 2.5b | 1.1 × 103d | 24.2b |
TNFR1KO | None | 2.21 × 108 | 91.0 ± 0.6 | 5.5 ± 0.3 | 1.5 ± 0.3 | 6.2 × 103 | 63.8 |
TNFR1KO | HK/483 | 1.18 × 108 | 63.0 ± 7.9b | 18.8 ± 4.8 | 7.8 ± 1.9b | 1.6 × 103d | 44.7 |
Four mice were infected with 1,000 MID50 of HK/483 virus; 6 days later, animals were euthanized for collection of blood and thymus. A single-cell suspension of thymocytes was prepared from each mouse; cells were then counted and subjected to flow cytometric analysis as described in Materials and Methods by gating of the lymphocyte population.
P ≤ 0.05 compared with uninfected group.
Four mice from each group were bled via the orbital plexus on days 0 and 6 p.i. Total peripheral white blood cell count analyses were performed using Turk's solution as previously described (59). Percentages of lymphocytes were determined by counting 100 white blood cells on fixed blood smear slides.
P ≤ 0.06 compared with uninfected group.