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. 1999 Feb 15;189(4):693–700. doi: 10.1084/jem.189.4.693

Table II.

CD34+ Blood Stem Cells Restore Activation of T Lymphocytes from LPS Nonresponders by LPS

Cell population DNA synthesis after stimulation with
None LPS Recall antigen
cpm/culture
Experiment 1
 PBMCs 680 ± 260 520 ± 90 12,080 ± 1,580
 CD34-depleted PBMCs 70 ± 10  80 ± 10 20,370 ± 2,680
 CD34-depleted PBMCs plus CD34-enriched cells 590 ± 130  8,380 ± 110  14,500 ± 90
Experiment 2
 PBMCs 550 ± 290 420 ± 10 32,170 ± 5,880
 CD34-depleted PBMCs 160 ± 100  600 ± 170 32,640 ± 3,950
 CD34-depleted PBMCs plus CD34-enriched cells  160 ± 40  2,230 ± 540 31,700 ± 2,640
Experiment 3
 PBMCs  140 ± 50 250 ± 80   2,110 ± 910
 CD34-depleted PBMCs  350 ± 40 390 ± 60   2,490 ± 120
 CD34-depleted PBMCs plus CD34-enriched cells 770 ± 240 12,010 ± 1,200  3,370 ± 1,030

Cells (106/ml) plus 10% accessory cells were stimulated with LPS (S. friedenau, 1 μg/ml), TT (donor 1, 1 Lf/ml), PPD (donor 2, 1 μg/ml), or BCG (donor 3, 4,000 CFU/ml) and cultured for 7 d in RPMI 1640 plus 10% HS in a final volume of 200 μl/culture. For the last 8 h of culture, cells were pulsed with [3H]TdR (0.2 μCi/culture), then harvested on glass filter mats, and the radioactivity was measured in a β-counter. Data are expressed as mean ± SD of three independent cultures.