First experience with non-invasive foetal RH genotyping from maternal peripheral blood in alloimmunised pregnancies
Authors:
I. Hromadníková 1; K. Veselá 1; B. Benešová 2; K. Nekovářová 4; D. Dušková 5; R. Vlk 3; I. Špálová 3; Romana Gerychová 6; A. Hakenová 8; M. Janoušková 9; Z. Rosenbaumová 10; P. Vlašín 11; A. Vlachová 12; P. Smejkal 7; V. Palásek 13; E. Langrová 14; E. Rožňáková 2; P. Calda 4
Authors‘ workplace:
Pediatrická klinika
1; Krevní banka
2; Gynekologicko-porodnická klinika, 2. LF UK a Fakultní nemocnice Motol, Praha
3; Gynekologicko-porodnická klinika a
4; Transfuzní oddělení, VFN a 1. LF UK, Praha
5; Gynekologicko-porodnická klinika a
6; Oddělení klinické hematologie, Fakultní nemocnice Brno
7; Transfúzní oddělení, Fakultní Thomayerova nemocnice, Praha
8; Transfuzní oddělení, Nemocnice Karlovy Vary
9; Ženská klinika, Masarykova nemocnice v Ústí n. L.
10; Gynekologická a ultrazvuková ambulance, Centrum prenatální diagnostiky, Brno
11; Transfuzní oddělení, Fakultní nemocnice Královské Vinohrady
12; Gynekologicko-porodnické oddělení a
13; Hematologicko-transfuzní oddělení, Nemocnice Kladno
14
Published in:
Transfuze Hematol. dnes,11, 2005, No. 1, p. 17-20.
Category:
Comprehensive Reports, Original Papers, Case Reports
Overview
In this prospective study, we described our first experience with non-invasive foetal RH genotyping in alloimmunised pregnancies by analysis of DNA extracted from maternal plasma samples by using real-time PCR and primers and probes targeted toward RHD and RHCE genes. We analysed 22 alloimmunised pregnant women (15 anti-D, 5 anti-D+C, 2 anti-E) within 11th and 33rd week of pregnancy and correlated the results with serological analysis of cord blood. Non-invasive prenatal foetal RHD and RHCE genotyping analysis of maternal plasma samples was in complete concordance with the analysis of cord blood in all alloimmunised pregnancies. Non-invasive foetal RHD and RHCE genotyping enables the identification of foetuses at risk of haemolytic disease of the newborn. An identification of negative foetuses may exclude the demand of invasive prenatal procedures.
Key words:
foetal DNA, haemolytic disease of the newborn, quantitative real-time PCR, maternal plasma, RHD gene, RHCE gene
Labels
Haematology Internal medicine Clinical oncologyArticle was published in
Transfusion and Haematology Today
2005 Issue 1
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