Mj. Divers et al., MATERNAL LEVELS OF SERUM-SOLUBLE CDS AND IL-2R ARE NOT SIGNIFICANTLY ELEVATED IN IDIOPATHIC PRETERM LABOR, European journal of obstetrics, gynecology, and reproductive biology, 62(2), 1995, pp. 209-212
Objective: To search for evidence of immune activation in idiopathic p
reterm term labour by measuring the soluble markers of T cell activati
on, CD8 (sCD8) and interleukin-2 receptor (sIL2R). Design : Serum sCD8
and sIL-2R were measured by commercial ELISA in subjects undergoing i
diopathic preterm labour (PTL; n=15) and normal term labour (TL; n=17)
. Two gestationally equivalent non-labouring groups were also included
representing preterm (PTC; n=10) and term (TC; n=10)controls. Possibl
e delayed responses in soluble activation markers were monitored in bl
ood samples taken 48 h after delivery in both labouring groups (PTLp;
n=9: TLp; n=9). Results: (1) Excluding the 48 h postpartum samples, no
statistically significant differences were revealed following a Krusk
all-Wallis analysis of variance (ANOVA) for levels of sIL-2R (P=0.093)
and sCD8 (P=0.098). Including the postpartum samples, however, gave s
tatistically significant differences for each (sIL-2R: P=0.033; sCD8:
P=0.006). (2) No statistically significant difference was revealed by
direct comparison of the two labouring groups alone (Wilcoxon-Mann-Whi
tney test: P > 0.05). (3) Significantly lower levels of sCD8 were foun
d in the PTL subgroup which had histological evidence of inflammation
(Wilcoxon-Mann-Whitney: P=0.003). Conclusions: Statistical analysis of
our data suggests that idiopathic preterm labour is not commonly asso
ciated with significant elevations in circulating sCD8 or sIL-2R level
s compared with normal term labour. Where significant changes in the l
evels of these markers do arise, our evidence points to a delayed effe
ct of labour per se rather than infection as the most probable cause.