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早产儿淋巴细胞亚群的发育。

Development of lymphocyte subpopulations in preterm infants.

机构信息

Department of Paediatrics, Jeroen Bosch Hospital, 's-Hertogenbosch, The Netherlands.

出版信息

Scand J Immunol. 2011 Jan;73(1):53-8. doi: 10.1111/j.1365-3083.2010.02473.x.

Abstract

In preterm neonates the immune system is thought to be less developed at birth, but very little is known about the actual size of lymphocyte subpopulations, and even less about the maturation of these subpopulations during the first months after a premature birth. To evaluate the development of lymphocyte subpopulations in preterm infants during the first 3 months after birth, we performed a prospective longitudinal study in two hospitals in the Netherlands. Preterm neonates (n = 38) of all post-menstrual ages were included and blood samples were taken from cord blood, and at 1 week, 6 weeks, and 3 months. Lymphocyte subpopulations were measured by four-colour flow cytometry. The data were compared with follow-up data obtained in healthy term neonates (n = 8), and with single samples from school age children (n = 5) and adults (n = 5). Overall, we found a similar pattern of post-natal development of lymphocyte subpopulations in the term and preterm infants. Both B lymphocytes and helper and cytotoxic T lymphocytes mainly consist of naive cells at birth and during the 3 months of follow-up in all neonatal age groups. So, the preterm immune system seems to be able to generate an outburst of naive T and B lymphocytes from the thymus and bone marrow within the same time span after the start of post-natal antigenic stimulation from the environment as the term immune system, but, with lower post-menstrual age, the absolute counts of naive helper T lymphocytes are lower.

摘要

在早产儿中,人们认为其出生时免疫系统发育不成熟,但对于淋巴细胞亚群的实际大小,甚至对于这些亚群在早产出生后的头几个月内的成熟情况,了解甚少。为了评估早产儿在出生后头 3 个月内淋巴细胞亚群的发育情况,我们在荷兰的两家医院进行了一项前瞻性纵向研究。纳入了所有早产儿(n=38),并采集脐带血、1 周、6 周和 3 个月时的血样。通过四色流式细胞术测量淋巴细胞亚群。将数据与健康足月新生儿(n=8)的随访数据以及来自学龄儿童(n=5)和成人(n=5)的单一样本进行比较。总体而言,我们发现足月和早产儿的淋巴细胞亚群在出生后具有相似的发育模式。在所有新生儿年龄组中,B 淋巴细胞以及辅助性和细胞毒性 T 淋巴细胞在出生时和 3 个月的随访期间主要由幼稚细胞组成。因此,早产儿的免疫系统似乎能够在与足月免疫系统相同的时间跨度内,从胸腺和骨髓中产生大量幼稚 T 和 B 淋巴细胞,以应对出生后环境中抗原的刺激,但由于胎龄较小,幼稚辅助性 T 淋巴细胞的绝对计数较低。

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