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. 2006 Oct;13(10):1098–1103. doi: 10.1128/CVI.00213-06

TABLE 1.

Flow cytometric analysis of responses to B. abortus strain 19 after initial and booster vaccinationa

Time postvaccination and animal group Mean no. of proliferating cells/10,000 PBMC ± SEMb
Total CD4+ CD8+ γδTCR+ IgM+
14 wk after initial vaccination
    Controls 893 ± 407 126 ± 46 25 ± 11 22 ± 15 881 ± 174
    RB51 vaccinates 1,833 ± 579* 449 ± 351 19 ± 15 335 ± 311 1,927 ± 432*
    S19 vaccinates 1,262 ± 467 64 ± 42 64 ± 64 59 ± 59 1,942 ± 607*
22 wk after initial vaccination
    Controls 367 ± 367 353 ± 325 76 ± 42 38 ± 27 273 ± 184
    RB51 vaccinates 2,161 ± 1,187* 1,354 ± 384* 381 ± 101* 89 ± 89 1,277 ± 333*
    S19 vaccinates 2,063 ± 405* 2,282 ± 245* 529 ± 253 11 ± 93 1,873 ± 212*
12 wk after booster vaccination
    Controls 0 ± 0 404 ± 322 88 ± 34 28 ± 42 141 ± 30
    RB51 vaccinates 0 ± 0 808 ± 488 232 ± 121 0 ± 0 467 ± 196
    S19 vaccinates 1,000 ± 541 691 ± 303 306 ± 134 24 ± 41 637 ± 266
a

PKH-67-labeled PBMC from elk vaccinated s.c. with saline (control), SRB51, or S19 (n = seven animals/treatment) and booster vaccinated 65 weeks later were incubated with 108 CFU of gamma-irradiated B. abortus strain 19 at 37°C and 5% CO2 for 7 days, labeled with monoclonal antibodies, and analyzed in a flow cytometer.

b

Means within a sampling time with an asterisk are significantly different (P < 0.05) from means of controls labeled with the same monoclonal antibody.