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基于 iPSC 的细胞治疗:向前迈出的重要一步。

iPSC-Based cell therapy: an important step forward.

机构信息

Director, NIH Center for Regenerative Medicine, 50 South Drive, Bethesda, MD 20892 USA.

出版信息

Stem Cell Reports. 2013 Oct 15;1(4):281-2. doi: 10.1016/j.stemcr.2013.10.002. eCollection 2013.

DOI:10.1016/j.stemcr.2013.10.002
PMID:24319663
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3849244/
Abstract

Morizane et al. (2013) show that donor-matched differentiated derivatives of induced pluripotent stem cells (iPSC) do not cause an immune response after transplantation, whereas transplantation of HLA-mismatched iPSC derivatives to the same site clearly does. The importance of these results is discussed in this commentary as we assess how best to move forward with iPSC-based cell therapy.

摘要

森谷等(2013)的研究表明,在移植后,与供体匹配的诱导多能干细胞(iPSC)分化衍生物不会引起免疫反应,而将 HLA 不匹配的 iPSC 衍生物移植到同一部位则会引起明显的免疫反应。在评估如何最好地推进基于 iPSC 的细胞治疗时,我们对这些结果的重要性进行了讨论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d9/3849244/684554e68a28/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d9/3849244/684554e68a28/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d9/3849244/684554e68a28/gr1.jpg

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本文引用的文献

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Stem Cell Reports. 2013 Sep 26;1(4):283-92. doi: 10.1016/j.stemcr.2013.08.007. eCollection 2013.
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Suppression of the imprinted gene NNAT and X-chromosome gene activation in isogenic human iPS cells.同源人诱导多能干细胞中 NNAT 印迹基因的抑制和 X 染色体基因的激活。
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