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. 1998 Nov;5(6):790–798. doi: 10.1128/cdli.5.6.790-798.1998

TABLE 1.

Effects of ethanol, acetaldehyde, and acetate on accessory cell function in clone 43 cellsa

Treatment (mM) Fold increase after stimulation with b:
PHA ConA PWM MAb 446 TT
None 135 ± 64 70 ± 34 28 ± 14 20 ± 9 6 ± 3
Ethanol
  25 103 ± 34 43 ± 21 18 ± 9 15 ± 7 4 ± 2
  75 40 ± 17 14 ± 7 13 ± 4 11 ± 3 3 ± 1.5
 150 14 ± 8 9 ± 5 7 ± 3 5 ± 3 1 ± 0.5
Acetaldehyde
  25 99 ± 37 45 ± 33 17 ± 1 14 ± 7 4.5 ± 1.7
  75 39 ± 16 15 ± 8 14 ± 5 13 ± 7 3.1 ± 1.6
 150 13 ± 7 8 ± 4 10 ± 5 10 ± 4 1.8 ± 0.9
Acetate
  25 101 ± 38 45 ± 23 20 ± 9 16 ± 8 4.5 ± 3.1
  75 42 ± 20 15 ± 8 12 ± 5 10 ± 4 3.1 ± 1.5
 150 15 ± 7 10 ± 6 7.5 ± 4 6 ± 2 1.1 ± 0.9
a

Some clone 43 cells (104) were maintained in culture, while others were treated with various concentrations (25, 75, and 150 mM) of ethanol, acetaldehyde, and acetate for 16 h, washed with PBS, cocultured with 105 monocyte-depleted PBMCs, and stimulated with PHA (1 μg/ml), ConA (1 μg/ml), PWM (1 μg/ml), and MAb 446 (anti-CD3 [5 μg/ml]) for 72 h. TT (4 μg/ml)-stimulated cultures were harvested after 5 days. [3H]thymidine (1 μCi) was added for the last 16 h, the cells were harvested, and the incorporated counts per minute were analyzed. 

b

Data are the means ± standard errors from the pooled data of three separate experiments and are expressed as fold increases (stimulation index) in accessory cell function over levels in unstimulated cultures.