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Clinical Tracking of Cell Transfer and Cell Transplantation: Trials and Tribulations
被引:91
作者:

Bulte, Jeff W. M.
论文数: 0 引用数: 0
h-index: 0
机构:
Johns Hopkins Univ, Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, Div MR Res,Cellular Imaging Sect, 217 Traylor Bldg,720 Rutland Ave, Baltimore, MD 21205 USA
Johns Hopkins Univ, Sch Med, Vasc Biol Program, Inst Cell Engn,Dept Chem & Biomol Engn, 217 Traylor Bldg,720 Rutland Ave, Baltimore, MD 21205 USA
Johns Hopkins Univ, Sch Med, Vasc Biol Program, Inst Cell Engn,Dept Biomed Engn, 217 Traylor Bldg,720 Rutland Ave, Baltimore, MD 21205 USA
Johns Hopkins Univ, Sch Med, Vasc Biol Program, Inst Cell Engn,Dept Oncol, 217 Traylor Bldg,720 Rutland Ave, Baltimore, MD 21205 USA Johns Hopkins Univ, Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, Div MR Res,Cellular Imaging Sect, 217 Traylor Bldg,720 Rutland Ave, Baltimore, MD 21205 USA

Daldrup-Link, Heike E.
论文数: 0 引用数: 0
h-index: 0
机构:
Stanford Univ, Dept Radiol, MIPS, Palo Alto, CA 94304 USA
Stanford Univ, Dept Pediat, Inst Stem Cell Biol & Regenerat Med, Palo Alto, CA 94304 USA Johns Hopkins Univ, Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, Div MR Res,Cellular Imaging Sect, 217 Traylor Bldg,720 Rutland Ave, Baltimore, MD 21205 USA
机构:
[1] Johns Hopkins Univ, Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, Div MR Res,Cellular Imaging Sect, 217 Traylor Bldg,720 Rutland Ave, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Vasc Biol Program, Inst Cell Engn,Dept Chem & Biomol Engn, 217 Traylor Bldg,720 Rutland Ave, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Vasc Biol Program, Inst Cell Engn,Dept Biomed Engn, 217 Traylor Bldg,720 Rutland Ave, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Vasc Biol Program, Inst Cell Engn,Dept Oncol, 217 Traylor Bldg,720 Rutland Ave, Baltimore, MD 21205 USA
[5] Stanford Univ, Dept Radiol, MIPS, Palo Alto, CA 94304 USA
[6] Stanford Univ, Dept Pediat, Inst Stem Cell Biol & Regenerat Med, Palo Alto, CA 94304 USA
来源:
关键词:
MESENCHYMAL STEM-CELLS;
NEPHROGENIC SYSTEMIC FIBROSIS;
MAGNETIC-RESONANCE TRACKING;
ARTICULAR-CARTILAGE REPAIR;
IN-VIVO;
MACROPHAGE INFILTRATION;
GADOLINIUM DEPOSITION;
PANCREATIC-ISLETS;
IMAGING TRACKING;
PROGENITOR CELLS;
D O I:
10.1148/radiol.2018180449
中图分类号:
R8 [特种医学];
R445 [影像诊断学];
学科分类号:
1002 ;
100207 ;
1009 ;
摘要:
Cell therapy has provided unprecedented opportunities for tissue repair and cancer therapy. Imaging tools for in vivo tracking of therapeutic cells have entered the clinic to evaluate therapeutic cell delivery and retention in patients. Thus far, clinical cell tracking studies have been a mere proof of principle of the feasibility of cell detection. This review centers around the main clinical queries associated with cell therapy: Have cells been delivered correctly at the targeted site of injection? Are cells still alive, and, if so, how many? Are cells being rejected by the host, and, if so, how severe is the immune response? For stem cell therapeutics, have cells differentiated into downstream cell lineages? Is there cell proliferation including tumor formation? At present, clinical cell tracking trials have only provided information on immediate cell delivery and short-term cell retention. The next big question is if these cell tracking tools can improve the clinical management of the patients and, if so, by how much, for how many, and for whom; in addition, it must be determined whether tracking therapeutic cells in every patient is needed. To become clinically relevant, it must now be demonstrated how cell tracking techniques can inform patient treatment and affect clinical outcomes. (C) RSNA, 2018
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页码:604 / 615
页数:12
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