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白细胞介素-12/15/18预激活的自然杀伤细胞在不匹配造血细胞移植小鼠模型中抑制移植物抗宿主病。

IL-12/15/18-preactivated NK cells suppress GvHD in a mouse model of mismatched hematopoietic cell transplantation.

作者信息

Hüber Christian M, Doisne Jean-Marc, Colucci Francesco

机构信息

Department of Obstetrics and Gynaecology, University of Cambridge School of Clinical Medicine, National Institute for Health Research (NIHR) Cambridge Biomedical Research Centre, Cambridge, UK.

出版信息

Eur J Immunol. 2015 Jun;45(6):1727-35. doi: 10.1002/eji.201445200. Epub 2015 Apr 17.


DOI:10.1002/eji.201445200
PMID:25778912
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4687420/
Abstract

Mismatched hematopoietic cell transplants for treating leukemia are complicated by graft versus host disease (GvHD). Here, we show that adoptively transferred IL-12/15/18-preactivated NK cells suppress GvHD in a mouse model of fully mismatched hematopoietic cell transplantation. These IL-12/15/18-preactivated NK cells maintained Eomesodermin (Eomes) and T-bet expression upon transfer and, while there was no evidence of direct killing of donor T cells or host DCs by the IL-12/15/18-preactivated NK cells, proliferation of donor T cells was inhibited. Strikingly, the graft versus leukemia effect mediated by donor T cells was retained, resulting in improved overall survival of mice that received lymphoma cells, donor allogeneic T cells, and IL-12/15/18-preactivated NK cells. These results suggest that IL-12/15/18-preactivated NK cells may be useful in improving immunotherapy of mismatched hematopoietic cell transplantation. Compared with previously proposed protocols, our findings suggest that in vitro NK-cell preactivation with this cytokine cocktail offers the significant advantage that cytokines do not need to be administered systemically to sustain NK-cell activity, thus avoiding toxicity.

摘要

用于治疗白血病的不匹配造血细胞移植会因移植物抗宿主病(GvHD)而变得复杂。在此,我们表明,过继转移经白细胞介素12/15/18预激活的自然杀伤(NK)细胞可在完全不匹配造血细胞移植的小鼠模型中抑制GvHD。这些经白细胞介素12/15/18预激活的NK细胞在转移后维持了胚外中胚层决定蛋白(Eomes)和T盒转录因子(T-bet)的表达,并且,虽然没有证据表明经白细胞介素12/15/18预激活的NK细胞直接杀伤供体T细胞或宿主树突状细胞(DC),但供体T细胞的增殖受到了抑制。引人注目的是,供体T细胞介导的移植物抗白血病效应得以保留,从而提高了接受淋巴瘤细胞、供体同种异体T细胞和经白细胞介素12/15/18预激活的NK细胞的小鼠的总体生存率。这些结果表明,经白细胞介素12/15/18预激活的NK细胞可能有助于改善不匹配造血细胞移植的免疫治疗。与先前提出的方案相比,我们的研究结果表明,用这种细胞因子鸡尾酒体外预激活NK细胞具有显著优势,即无需全身性给予细胞因子来维持NK细胞活性,从而避免毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea0e/4687420/fdd68151dfd4/eji0045-1727-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea0e/4687420/2277b78231c0/eji0045-1727-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea0e/4687420/a59dcfb56f47/eji0045-1727-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea0e/4687420/83f00705017e/eji0045-1727-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea0e/4687420/976851affa8c/eji0045-1727-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea0e/4687420/da20cde76dfe/eji0045-1727-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea0e/4687420/fdd68151dfd4/eji0045-1727-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea0e/4687420/2277b78231c0/eji0045-1727-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea0e/4687420/a59dcfb56f47/eji0045-1727-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea0e/4687420/83f00705017e/eji0045-1727-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea0e/4687420/976851affa8c/eji0045-1727-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea0e/4687420/da20cde76dfe/eji0045-1727-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea0e/4687420/fdd68151dfd4/eji0045-1727-f6.jpg

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IL-12/15/18-preactivated NK cells suppress GvHD in a mouse model of mismatched hematopoietic cell transplantation.

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[7]
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[8]
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本文引用的文献

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J Leukoc Biol. 2011-6-28

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