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. 2003 Apr;77(7):4004–4014. doi: 10.1128/JVI.77.7.4004-4014.2003

TABLE 3.

Characterization of infiltrating T cells within secondary lymphoid tissuesa

Organ Mouse Day p.i. No. of CD4+ cells No. of CD8+ cells No. of CD8+ (S510-518) cells
Lymph nodesb CCL3+/+ 7 (8.4 ± 0.1) × 105 (5.7 ± 0.4) × 105 (3.3 ± 0.1) × 104
12 (9.6 ± 0.3) × 104 (7.2 ± 0.3) × 104 (5.5 ± 0.8) × 103
CCL3−/− 7 (8.2 ± 0.2) × 105 (5.0 ± 0.1) × 105 (4.0 ± 0.1) × 104
12 (9.1 ± 0.2) × 105 (5.8 ± 0.2) × 105 (1.3 ± 0.2) × 105d
Spleenc CCL3+/+ 7 (7.8 ± 0.5) × 106 (2.3 ± 0.2) × 106 (1.6 ± 0.3) × 105
12 (6.1 ± 0.3) × 105 (6.6 ± 0.3) × 105 (2.0 ± 0.4) × 104
CCL3−/− 7 (5.1 ± 0.1) × 106 (2.5 ± 0.6) × 106 (4.2 ± 0.2) × 105d
12 (6.3 ± 0.3) × 106 (2.6 ± 0.3) × 106 (7.0 ± 0.6) × 105d
a

Total cells were determined by multiplying the percentage of doubly positive cells by the number of total lymphocytes isolated.

b

Characterization, by flow cytometric analysis, of mononuclear cells within the CLN following i.c. infection with MHV. The data are representative of three separate experiments with a minimum of three mice per group and are means ± SEM.

c

Characterization, by flow cytometric analysis, of mononuclear cells within the spleen following i.p. immunization with MHV. The data are representative of three separate experiments with a minimum of three mice per group and are means ± SEM.

d

P ≤ 0.01 compared with results for CCL3+/+ mice.