Linch D C, Beverley P C, Levinsky R J, Rodeck C H
Prenat Diagn. 1982 Jul;2(3):211-8. doi: 10.1002/pd.1970020310.
Recent technological advances allow the detection and quantitation of subsets of leucocytes using monoclonal antibodies. We have taken advantage of this to study the ontogeny of fetal blood leucocytes, using very small blood samples obtained at fetoscopy. By 14 weeks gestation T cells represent 35 per cent or more of fetal leucocytes and the distribution of the helper/inducer and suppressor/cytotoxic subsets is similar to that of adults. B lymphocytes before 16 1/2 weeks are low (4-20 per cent), but rise to a mean of 28 per cent in 17-26 week fetuses. Granulocytic cells, many of which are phenotypically immature, represent 18-34 per cent of total leucocytes. The methodology employed is very reliable and offers the opportunity for the prenatal diagnosis of some immunodeficiency disorders, since using the same reagents we have diagnosed children with severe combined immunodeficiency shortly after birth.
最近的技术进步使得使用单克隆抗体检测和定量白细胞亚群成为可能。我们利用这一点,通过胎儿镜检查获取的非常少量的血样来研究胎儿血液白细胞的个体发生。到妊娠14周时,T细胞占胎儿白细胞的35%或更多,辅助/诱导亚群和抑制/细胞毒性亚群的分布与成年人相似。16.5周之前的B淋巴细胞比例较低(4%-20%),但在17-26周的胎儿中平均升至28%。粒细胞,其中许多在表型上不成熟,占白细胞总数的18%-34%。所采用的方法非常可靠,为一些免疫缺陷疾病的产前诊断提供了机会,因为使用相同的试剂,我们在出生后不久就诊断出患有严重联合免疫缺陷的儿童。