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. 2006 May;74(5):2751–2759. doi: 10.1128/IAI.74.5.2751-2759.2006

TABLE 1.

Protection against a challenge M. tuberculosis infection in CD4−/− mice reconstituted with CD4+ T cells and vaccinated with Ag85B DNAa

Mouse treatment parameter Log10 mRLU (SD)b
Spleen
Lungs
WT (4 wk) CD4−/− (4 wk) CD4−/− (8 wk) WT (4 wk) CD4−/− (4 wk) CD4−/− (8 wk)
Naive (n = 4) 3.57 (0.13) 4.72 (0.29) 4.74 (0.47) 4.80 (0.17) 5.08 (0.40) 5.45 (0.07)
Ag85B DNA (n = 4) 3.42 (0.03) 4.96 (0.39) 5.33 (0.14) 4.20 (0.34)* 4.75 (0.40) 5.25 (0.30)
BCG (n = 4) 3.43 (0.09) 3.73 (0.26)** ND 3.71 (0.13)** 3.80 (0.30)** ND
AT (20 × 106 CD4+ T cells) (n = 3) 4.37 (0.14) 4.49 (0.14) 5.24 (0.16) 5.40 (0.10)
AT (20 × 106 CD4+ T cells) + control DNA (n = 4) ND 4.58 (0.3) ND 5.63 (0.22)
AT (5 × 106 CD4+ T cells) + Ag85B DNA (n = 4) 4.57 (0.15) ND 5.17 (0.33) ND
AT (20 × 106 CD4+ T cells) + Ag85B DNAc 4.28 (0.38)* 4.1 (0.24)** 5.22 (0.29) 5.05 (0.50)
a

Eight weeks after the third dose of pDNA vaccination and 8 weeks after BCG vaccination, mice received a luminescent M. tuberculosis challenge (2 × 105 CFU = 5 log10 mRLU/mouse, intravenously). Four and eight weeks later, viable bacterial counts in spleen and lungs were determined by luminescence.

b

*, P < 0.05; **, P <0.01 (compared to Ag85B DNA-vaccinated CD4−/− mice for reconstituted CD4−/− mice and compared to naïve mice for the other groups); ND, not done.

c

n = 5 at 4 weeks; n = 4 at 8 weeks.