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. 2010 Jan 27;17(4):618–625. doi: 10.1128/CVI.00368-09

FIG. 1.

FIG. 1.

Changes in CD4 and CD8 T-cell subsets expressing markers for TEM and TCM in target organs over the course of the study. (A) Representative gating strategy to identify and quantitate CD62Llo CCR7lo CD44hi TEM and CD62Lhi CCR7hi CD44hi TCM populations. (B) Numbers of CD4 TEM, CD8 TEM, CD4 TCM, and CD8 TCM in the lungs versus time of the infection. Test groups were mice chronically infected with M. tuberculosis (▪), mice that had been subcutaneously vaccinated with BCG (▴), or age-matched uninfected controls (▾). In each case, the data point represents the log10 mean value for cells recovered from the lungs or other organs of four or five mice; standard errors of the means (SEM) are omitted for clarity and did not exceed 10%. In all cases, numbers of cells were increased in the infected animals compared to uninfected age-matched controls (for M. tuberculosis infection at all time points, P < 0.01 or lower for TEM values and P < 0.02 for TCM values; for BCG, P < 0.04 [day 40 CD4 and CD8 TEM] and P < 0.03 or lower [for all other data points]).