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未来组织相容性干细胞治疗的策略。

Strategies for future histocompatible stem cell therapy.

作者信息

Nehlin Jan O, Barington Torben

机构信息

Center for Stem Cell Treatment, Department of Clinical Immunology, University of Southern Denmark, Denmark.

出版信息

Biogerontology. 2009 Aug;10(4):339-76. doi: 10.1007/s10522-009-9213-7. Epub 2009 Feb 15.

DOI:10.1007/s10522-009-9213-7
PMID:19219637
Abstract

Stem cell therapy based on the safe and unlimited self-renewal of human pluripotent stem cells is envisioned for future use in tissue or organ replacement after injury or disease. A gradual decline of regenerative capacity has been documented among the adult stem cell population in some body organs during the aging process. Recent progress in human somatic cell nuclear transfer and inducible pluripotent stem cell technologies has shown that patient-derived nuclei or somatic cells can be reprogrammed in vitro to become pluripotent stem cells, from which the three germ layer lineages can be generated, genetically identical to the recipient. Once differentiation protocols and culture conditions can be defined and optimized, patient-histocompatible pluripotent stem cells could be directed towards virtually every cell type in the human body. Harnessing this capability to enrich for given cells within a developmental lineage, would facilitate the transplantation of organ/tissue-specific adult stem cells or terminally differentiated somatic cells to improve the function of diseased organs or tissues in an individual. Here, we present an overview of various experimental cell therapy technologies based on the use of patient-histocompatible stem cells, the pending issues needed to be dealt with before clinical trials can be initiated, evidence for the loss and/or aging of the stem cell pool and some of the possible uses of human pluripotent stem cell-derivatives aimed at curing disease and improving health.

摘要

基于人类多能干细胞安全且无限自我更新的干细胞疗法,有望在未来用于损伤或疾病后的组织或器官替代。在衰老过程中,已记录到某些身体器官中的成体干细胞群体的再生能力逐渐下降。人类体细胞克隆和诱导多能干细胞技术的最新进展表明,患者来源的细胞核或体细胞可以在体外重编程为多能干细胞,从中可以产生三个胚层谱系,与受体基因相同。一旦能够定义和优化分化方案及培养条件,与患者组织相容的多能干细胞几乎可以定向分化为人体的每一种细胞类型。利用这种能力在发育谱系中富集特定细胞,将有助于移植器官/组织特异性成体干细胞或终末分化的体细胞,以改善个体中患病器官或组织的功能。在此,我们概述了基于使用与患者组织相容的干细胞的各种实验性细胞疗法技术、在启动临床试验之前需要解决的悬而未决的问题、干细胞池损耗和/或老化的证据,以及人类多能干细胞衍生物在治疗疾病和改善健康方面的一些可能用途。

相似文献

1
Strategies for future histocompatible stem cell therapy.未来组织相容性干细胞治疗的策略。
Biogerontology. 2009 Aug;10(4):339-76. doi: 10.1007/s10522-009-9213-7. Epub 2009 Feb 15.
2
Transplantation tolerance in an age of induced pluripotency.诱导多能性时代的移植耐受性。
Curr Opin Organ Transplant. 2009 Aug;14(4):321-5. doi: 10.1097/MOT.0b013e32832e9424.
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Adult reserve stem cells and their potential for tissue engineering.成人储备干细胞及其在组织工程中的潜力。
Cell Biochem Biophys. 2004;40(1):1-80. doi: 10.1385/CBB:40:1:1.
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The use of stem cells in kidney disease.干细胞在肾脏疾病中的应用。
Curr Opin Organ Transplant. 2009 Feb;14(1):72-8. doi: 10.1097/MOT.0b013e328320d2f5.
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Challenges of stem cell therapy for spinal cord injury: human embryonic stem cells, endogenous neural stem cells, or induced pluripotent stem cells?脊髓损伤干细胞治疗的挑战:人胚胎干细胞、内源性神经干细胞还是诱导多能干细胞?
Stem Cells. 2010 Jan;28(1):93-9. doi: 10.1002/stem.253.
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Embryonic and adult stem cell therapy.胚胎和成体干细胞治疗。
J Allergy Clin Immunol. 2010 Feb;125(2 Suppl 2):S336-44. doi: 10.1016/j.jaci.2009.09.032. Epub 2010 Jan 12.
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Very small embryonic-like stem cells for regenerative medicine: WO2010039241.用于再生医学的非常小的胚胎样干细胞:WO2010039241。
Expert Opin Ther Pat. 2010 Aug;20(8):1103-6. doi: 10.1517/13543776.2010.495122.
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A dive into the stem cells world.深入干细胞世界。
Panminerva Med. 2009 Mar;51(1):1-3.
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Exploiting pluripotency for therapeutic gain.利用多能性获得治疗收益。
Panminerva Med. 2010 Jun;52(2):167-73.
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Culture systems for pluripotent stem cells.多能干细胞的培养系统。
J Biosci Bioeng. 2005 Jul;100(1):12-27. doi: 10.1263/jbb.100.12.

引用本文的文献

1
Future research and therapeutic applications of human stem cells: general, regulatory, and bioethical aspects.人类干细胞的未来研究和治疗应用:一般、监管和生物伦理方面。
J Transl Med. 2010 Dec 10;8:131. doi: 10.1186/1479-5876-8-131.