首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Patterns of graft infiltration and cytokine gene expression during the first 10 days of kidney transplantation.
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Patterns of graft infiltration and cytokine gene expression during the first 10 days of kidney transplantation.

机译:肾脏移植前10天的移植物浸润和细胞因子基因表达模式。

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Understanding of the events preceding acute cellular rejection of kidney transplants would be useful in the development of immunosuppressive strategies to prevent rejection. Information about these events in humans has been scarce, because of the lack of early, serial, biopsy samples. We took daily fine needle aspirates from kidney allografts for the first 10 days after transplant. Samples were analyzed by morphological cytology of graft-infiltrating cells, and reverse transcriptase-polymerase chain reaction for detection of interleukin (IL)-2, IL-4, IL-6, IL-10, and gamma-interferon gene expression. During the first 4 days, all of the grafts developed a low-grade monocyte-rich mononuclear cell infiltrate, accompanied by IL-10 gene expression. Thereafter, the infiltrates either remained stable or intensified. Of the 13 grafts with dense infiltrates, seven developed graft dysfunction. The remaining six did not, despite significant interstitial infiltrates. Both rejecting and nonrejecting dense infiltrates were associated with a biphasic pattern of IL-2 and gamma-interferon gene expression, preceding and accompanying lymphocytic graft infiltration. Grafts that did not develop dense infiltrates had no detectable IL-2 or gamma-interferon gene expression and did not suffer cellular rejection during the study period. The development of both rejecting and nonrejecting infiltrates was strongly associated with DR mismatches between donor and recipient. IL-2 and gamma-interferon gene expression are necessary, but not sufficient, for the development of acute cellular rejection in the first 10 days of kidney transplantation, and are more closely associated with the period leading up to rejection than with the period of graft dysfunction.
机译:了解肾移植急性细胞排斥之前的事件将有助于免疫抑制策略的发展,以防止排斥。由于缺乏早期的,连续的活检样本,有关人类中这些事件的信息十分稀少。移植后的前10天,我们每天从肾脏同种异体移植物中抽取细针。通过移植物浸润细胞的形态细胞学分析样品,并通过逆转录酶-聚合酶链反应检测白介素(IL)-2,IL-4,IL-6,IL-10和γ-干扰素基因表达。在最初的4天中,所有移植物均发生了低级的富含单核细胞的单核细胞浸润,并伴有IL-10基因表达。此后,浸润物保持稳定或增强。在13例浸润密集的移植物中,有7例发生移植功能障碍。尽管有大量的间质浸润,其余的六个却没有。排斥性和非排斥性密集浸润都与IL-2和γ-干扰素基因表达的双相模式有关,在淋巴细胞移植物浸润之前和之后。在研究期间,未发生密集浸润的移植物没有可检测的IL-2或γ-干扰素基因表达,也没有遭受细胞排斥。排斥和非排斥浸润的发展都与供体和受体之间的DR失配密切相关。 IL-2和γ-干扰素基因表达对于肾脏移植的前10天急性细胞排斥反应的发展是必要的,但还不够,并且与导致排斥反应的时期相比,与移植时期的关联更紧密功能障碍。

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