Pre-eclampsia is a disorder of human pregnancy occuring in 5-10 % of all births, and represents the leading cause of infant
morbidity and mortality and maternal death. In pre-eclampsia, invasion of fetal trophoblasts into maternal arteries during
early pregnancy is shallow or absent. Here we examined the hypothesis that
HLA-G, a non-classical class I
HLA expressed in cytotrophoblasts, may act as a key gene in pre-eclampsia. We analysed
HLA-G at the level of transcription and genotyped a silent CAC-CAT polymorphism in exon 3 and a 14-bp insertion/deletion in the
3′ untranslated region. A deficit in levels of the
HLA-G3 transcript was observed in mild pre-eclampsia compared to normal placentas. The distribution of
HLA-G polymorphisms was different between normal and pre-eclampsia samples. A correlation between the alteration in transcription
of the
HLA-G gene and certain
HLA-G genotypes was also observed. Thus we provide the first evidence for a possible role of
HLA-G in genetic susceptibility to, and pathogenesis of pre-eclampsia.
Key words: Pre-eclampsia; HLA-G; alternative splicing; polymorphism.
Received 8 May 2001; received after revision 7 September 2001; accepted 11 September 2001