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Laham N, Brennecke SP, Bendtzen K, Rice GE. Tumour necrosis factor
during human pregnancy and labour: maternal plasma and amniotic fluid concentrations and release from intrauterine tissues. Eur J Endocrinol 1994;131:607–14. ISSN 0804–4643
The aims of this study were: to quantify immunoreactive tumour necrosis factor
(TNF-
) concentrations in maternal plasma and amniotic fluid obtained from women during pregnancy and labour, both at term and preterm; and to establish the effects of bacterial endotoxin and cytokines on the in vitro release of TNF-
from intrauterine tissues. Maternal plasma TNF-
concentrations did not change during pregnancy (457.2 ± 102.9 ng/l, mean ± SEM, N = 52) or at the time of labour (543.5 ± 138.6 ng/l, N = 43). In contrast, amniotic fluid TNF-
concentrations increased significantly (p < 0.05) during pregnancy (early pregnancy, EP, 93.0 ± 24.8 ng/l, N = 7; preterm not-in-labour, PNIL, 186.8 ± 42.9 ng/l, N = 16; term not-in-labour, TNIL, 499.7 ± 150.9 ng/l, N = 13) and in association with preterm labour (preterm in-labour, PIL, 958.7 ± 575.6 ng/l, N = 5 vs PNIL, 186.8 ± 42.9 ng/l, N = 16). Choriodecidual and placental explants (N = 3) maintained in in vitro culture released TNF-
Furthermore, the release of TNF-
-
was increased significantly (p < 0.05) by bacterial endotoxin (lipopolysaccharide, 10 ng/l–10 mg/l) but was not affected by the following cytokines at the indicated doses: interleukin-1
(0.28 nmol/l), interleukin-6 (12.5 nmol/l), granulocyte colony-stimulating factor (2.5 nmol/l), granulocyte–macrophage colonystimulating factor (35 nmol/l), macrophage colony-stimulating factor (1.2 nmol/l), leukaemia inhibitory factor (0.45 nmol/l) and transforming growth factor-β (0.4 nmol/l). The data obtained in this study are consistent with a role for TNF-
in both preterm labour and normal labour at term.
N Laham, Department of Perinatal Medicine, Royal Women's Hospital, 132 Grattan Street, Carlton, Victoria, Australia 3053
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