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首页> 外文期刊>Hepatology: Official Journal of the American Association for the Study of Liver Diseases >Systemic transmigration of allosensitizing donor dendritic cells to host secondary lymphoid organs after rat liver transplantation
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Systemic transmigration of allosensitizing donor dendritic cells to host secondary lymphoid organs after rat liver transplantation

机译:大鼠肝移植后,同种异体供体树突状细胞向宿主次级淋巴器官的系统性迁移

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摘要

Donor dendritic cell (DC) migration and allosensitization in host secondary lymphoid organs after liver transplantation are ill defined. We used rat models to investigate graft-derived cells and intrahost allosensitization. Liver transplantation induced diffuse blood-borne migration of donor major histocompatibility class II antigen-positive (MHCII+) cells and MHCI+ cells from the graft to host secondary lymphoid organs, not only the spleen, but also lymph nodes and Peyer's patches. The migrated MHCII+ cells included DCs and some T cells and B cells. The DCs formed clusters with host BrdU(+) cells where they up-regulated CD86(+), and a CD8(+) T cell proliferative response originated within 24 hours after liver transplantation, demonstrating that these DCs can quickly mature and trigger direct allosensitization in host lymphoid organs. Transfer of allogeneic bone marrow cells also induced DC transmigration and a similar host response. In contrast, allogeneic thoracic duct lymph cells contained many fewer transmigrating DCs, and their transfer induced a comparable T cell response but significantly weaker CD8(+) T cell proliferation. Thus, there is a different outcome via the indirect pathway by host DCs that have captured donor alloantigens. Conclusion: The rat liver as well as bone marrow contains an immature DC population that can systemically transmigrate through blood vessel walls of the host secondary lymphoid organs, quickly mature, and induce diffuse intrahost CD8(+) T cell responses, which may promote graft rejection.
机译:肝移植后宿主次生淋巴器官中的供体树突状细胞(DC)迁移和同种异体化尚不明确。我们使用大鼠模型来研究移植物衍生的细胞和宿主内部的同种增敏作用。肝移植引起供体主要组织相容性II类抗原阳性(MHCII +)细胞和MHCI +细胞从移植物扩散到宿主次生淋巴器官,不仅是脾脏,而且还包括淋巴结和Peyer斑块。迁移的MHCII +细胞包括DC以及一些T细胞和B细胞。 DCs与宿主BrdU(+)细胞形成簇,在那里它们上调CD86(+),以及CD8(+)T细胞增殖反应在肝移植后24小时内产生,表明这些DCs可以迅速成熟并触发直接同种异体增敏作用在宿主淋巴器官中。同种异体骨髓细胞的转移也诱导DC迁移和类似的宿主反应。相比之下,同种异体胸导管淋巴细胞包含更少的迁移DC,并且它们的转移诱导了可比的T细胞反应,但CD8(+)T细胞增殖明显减弱。因此,已经捕获供体同种抗原的宿主DC通过间接途径存在不同的结果。结论:大鼠肝脏和骨髓中含有不成熟的DC种群,可以通过宿主次生淋巴器官的血管壁系统迁移,迅速成熟并诱导弥漫性宿主内CD8(+)T细胞反应,这可能促进移植排斥。

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