Table II.
Study point | n | CD3+ (%) | CD4+ (%) | CD8+ (%) | CD4+/CD8+ | |
---|---|---|---|---|---|---|
Control | 0 month | 24 | 62.67 ±14.58 | 34.64 ±11.05 | 24.26 ±11.00 | 1.73 ±0.92 |
1 month | 21 | 61.55 ±13.94 | 33.32 ±9.70 | 25.99 ±12.70 | 1.52 ±0.58 | |
3 month | 22 | 62.74 ±13.77 | 34.15 ±11.89 | 25.00 ±10.11 | 1.43 ±0.67 | |
7 month | 21 | 63.07 ±14.16 | 35.22 ±11.33 | 24.58 ±9.83 | 1.61 ±0.76 | |
rhIL-2 | 0 month | 22 | 59.85 ±16.09 | 35.41 ±9.99 | 23.48 ±7.20 | 1.66 ±0.77 |
1 month | 21 | 63.93 ±11.15 | 36.13 ±8.66 | 24.47 ±7.72 | 1.63 ±0.70 | |
3 month | 22 | 57.04 ±15.94 | 31.01 ±9.90 | 24.63 ±8.42 | 1.47 ±0.87 | |
7 month | 22 | 58.82 ±12.29 | 31.58 ±9.28 | 24.27 ±7.49 | 1.41 ±0.61 |
Data are expressed as mean ± standard deviation. The proportions of CD3+, CD4+, CD8+, and CD4+/CD8+ are assessed in different numbers of patients prior to the study and during TB treatment. MDR-TB – multidrug-resistant tuberculosis. rhIL-2 – recombinant human interleukin-2.