Williams J, Medearis A L, Chu W H, Kovacs G D, Kaback M M
Prenat Diagn. 1987 Jun;7(5):315-22. doi: 10.1002/pd.1970070504.
Maternal cell contamination of chorionic villi (CV) samples used for first trimester prenatal diagnosis can cause obvious and/or unrecognized diagnostic dilemmas. The purpose of this investigation is to assess the frequency of maternal cell contamination (MCC) in chorionic villus samples and to evaluate selected parameters which might predict where contamination is more likely to have occurred. Maternal lymphocytes, chorionic villi from ultrasonically directed transcervical catheter aspiration, and fetal tissue were obtained at 8-11 weeks gestation from 45 patients undergoing elective termination. Quinacrine (Q) banded metaphases were compared from duplicate direct preparations of chorionic villi; cultured chorionic villi, fetal fibroblast tissue cultures, and maternal lymphocyte cultures. Q-polymorphisms in metaphase chromosomes were 100 per cent concordant between fetal tissue and direct CV preparation. However, evidence for maternal cell contamination occurred in 13.1 per cent of cultured chorionic villi preparations where polymorphisms were found to be identical between maternal and cultured CV and both distinct from fetal tissue preparations. Where MCC was identified, it was noted that CV cell cultivation interval was prolonged (24.2 +/- 6.8 days) compared with non-contaminated cultures (14.1 +/- 4.4 days) (p less than 0.05). We conclude that maternal cell contamination is a significant problem with chorionic villus sampling. Where direct preparations are not employed or when cultures are 'slow growing', MCC may be a significant and unrecognized complication re: fetal diagnosis. Direct preparations, multiple cultures, quinacrine banding, and maternal Q-polymorphism comparisons can minimize diagnostic dilemmas secondary to maternal cell contamination.(ABSTRACT TRUNCATED AT 250 WORDS)
用于孕早期产前诊断的绒毛膜绒毛(CV)样本中的母体细胞污染可导致明显的和/或未被识别的诊断困境。本研究的目的是评估绒毛膜绒毛样本中母体细胞污染(MCC)的频率,并评估可能预测污染更易发生部位的选定参数。在妊娠8 - 11周时,从45例接受选择性终止妊娠的患者中获取母体淋巴细胞、经超声引导经宫颈导管抽吸获得的绒毛膜绒毛以及胎儿组织。对绒毛膜绒毛的重复直接制片、培养的绒毛膜绒毛、胎儿成纤维细胞组织培养物和母体淋巴细胞培养物的喹吖因(Q)带中期进行比较。中期染色体中的Q多态性在胎儿组织和直接的CV制片之间100%一致。然而,在13.1%的培养绒毛膜绒毛制片中发现了母体细胞污染的证据,其中母体和培养的CV之间的多态性相同,且均与胎儿组织制片不同。在识别出MCC的情况下,注意到与未受污染的培养物(14.1 +/- 4.4天)相比,CV细胞培养间隔延长(24.2 +/- 6.8天)(p < 0.05)。我们得出结论,母体细胞污染是绒毛膜绒毛取样的一个重要问题。在不采用直接制片或培养物“生长缓慢”时,MCC可能是胎儿诊断中一个重要且未被识别的并发症。直接制片、多次培养、喹吖因带型分析和母体Q多态性比较可将母体细胞污染导致的诊断困境降至最低。(摘要截短至250字)