Naumova Anna V, Modo Michel, Moore Anna, Murry Charles E, Frank Joseph A
1] Department of Radiology, University of Washington, Seattle, Washington, USA. [2] Center for Cardiovascular Biology, University of Washington, Seattle, Washington, USA. [3] Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, Washington, USA.
1] McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA. [2] Centre for the Neural Basis of Cognition, University of Pittsburgh, Pittsburgh, Pennsylvania, USA. [3] Department of Radiology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA. [4] Department of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Nat Biotechnol. 2014 Aug;32(8):804-18. doi: 10.1038/nbt.2993.
In regenerative medicine, clinical imaging is indispensable for characterizing damaged tissue and for measuring the safety and efficacy of therapy. However, the ability to track the fate and function of transplanted cells with current technologies is limited. Exogenous contrast labels such as nanoparticles give a strong signal in the short term but are unreliable long term. Genetically encoded labels are good both short- and long-term in animals, but in the human setting they raise regulatory issues related to the safety of genomic integration and potential immunogenicity of reporter proteins. Imaging studies in brain, heart and islets share a common set of challenges, including developing novel labeling approaches to improve detection thresholds and early delineation of toxicity and function. Key areas for future research include addressing safety concerns associated with genetic labels and developing methods to follow cell survival, differentiation and integration with host tissue. Imaging may bridge the gap between cell therapies and health outcomes by elucidating mechanisms of action through longitudinal monitoring.
在再生医学中,临床成像对于表征受损组织以及评估治疗的安全性和有效性不可或缺。然而,利用现有技术追踪移植细胞的命运和功能的能力有限。诸如纳米颗粒之类的外源性对比标记在短期内能给出强烈信号,但长期来看并不可靠。基因编码标记在动物体内的短期和长期表现都很好,但在人体环境中,它们会引发与基因组整合安全性及报告蛋白潜在免疫原性相关的监管问题。脑、心脏和胰岛的成像研究面临一系列共同挑战,包括开发新的标记方法以提高检测阈值并尽早确定毒性和功能。未来研究的关键领域包括解决与基因标记相关的安全问题,以及开发追踪细胞存活、分化和与宿主组织整合的方法。成像可通过纵向监测阐明作用机制,从而弥合细胞疗法与健康结果之间的差距。