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出生时的免疫系统转换会引发外周T细胞寿命的变化。

An immune system switch at birth triggers a change in the lifespan of peripheral T cells.

作者信息

Cahill R N, Kimpton W G, Cunningham C P, Washington E A

机构信息

Laboratory for Fetal and Neonatal Immunology, The University of Melbourne, Cnr Flemington Road and Park Drive, Parkville, Victoria, 3052, Australia.

出版信息

Semin Immunol. 1997 Dec;9(6):355-63. doi: 10.1006/smim.1997.0093.

DOI:10.1006/smim.1997.0093
PMID:9405264
Abstract

Lymphocyte recirculation is an essential element in the integration of immune responses and is an absolute requirement for the development of systemic memory in postnatal animals. During foetal life a large pool of recirculating T cells develops and migration pathways of naive T cells to skin and peripheral tissues as well as LN are established. At birth a process is triggered whereby naive fetal T cells are rapidly lost from the circulating pool and are replaced by newly arriving T cells which have been formed since birth. At present our data suggest that the thymic export in the fetus creates a pool of long-lived naive T cells of wide diversity. The situation in neonatal lambs is more complex since the thymus is exporting large numbers of short-lived thymic emigrants which enter a peripheral T-cell population where many T cells are dividing.

摘要

淋巴细胞再循环是免疫反应整合的一个基本要素,也是出生后动物全身记忆形成的绝对必要条件。在胎儿期,大量循环T细胞池形成,幼稚T细胞向皮肤、外周组织以及淋巴结的迁移途径得以建立。出生时,一个过程被触发,幼稚胎儿T细胞迅速从循环池中消失,并被出生后新形成的T细胞所取代。目前我们的数据表明,胎儿期胸腺输出产生了一个高度多样化的长寿幼稚T细胞池。新生羔羊的情况更为复杂,因为胸腺正在输出大量短命的胸腺迁出细胞,这些细胞进入外周T细胞群体,其中许多T细胞正在分裂。

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An immune system switch at birth triggers a change in the lifespan of peripheral T cells.出生时的免疫系统转换会引发外周T细胞寿命的变化。
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