Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2015 Sep 15;142(18):3077-84.
doi: 10.1242/dev.126482.

The advancement of human pluripotent stem cell-derived therapies into the clinic

Affiliations

The advancement of human pluripotent stem cell-derived therapies into the clinic

R Scott Thies et al. Development. .

Erratum in

Abstract

Human pluripotent stem cells (hPSCs) offer many potential applications for drug screening and 'disease in a dish' assay capabilities. However, a more ambitious goal is to develop cell therapeutics using hPSCs to generate and replace somatic cells that are lost as a result of disease or injury. This Spotlight article will describe the state of progress of some of the hPSC-derived therapeutics that offer the most promise for clinical use. Lessons from developmental biology have been instrumental in identifying signaling molecules that can guide these differentiation processes in vitro, and will be described in the context of these cell therapy programs.

Keywords: Clinical medicine; HPSC-cardiomyocytes; Human Pluripotent Stem Cell.

PubMed Disclaimer

Figures

Fig. 1.
Fig. 1.
hPSC-derived cell therapeutics advancing to clinical testing. hPSC-derived cell therapeutics advancing to clinical testing include retinal pigment epithelium (RPE) for retinal degenerative diseases, dopaminergic neurons (Neurons) for Parkinson's disease, cardiomyocytes for heart disease, oligodendrocyte progenitor cells (OPCs) for spinal cord injury and β-islet cells (β cells) for diabetes.

References

    1. All A. H., Gharibani P., Gupta S., Bazley F. A., Pashai N., Chou B.-K., Shah S., Resar L. M., Cheng L., Gearheart J. D. et al. (2015). Early intervention for spinal cord injury with human induced pluripotent stem cells oligodendrocyte progenitors. PLoS ONE 10, e116933 10.1371/journal.pone.0116933 - DOI - PMC - PubMed
    1. Anderson M. E., Goldhaber J., Houser S. R., Puceat M. and Sussman M. A. (2014). Embryonic stem cell-derived cardiac myocytes are not ready for human trials. Circ. Res. 115, 335-338. 10.1161/CIRCRESAHA.114.304616 - DOI - PMC - PubMed
    1. Armstrong J. D., Meyer D., Xu S. and Elfervig J. L. (1998). Long-term follow-up of Stargardt's disease and fundus flavimaculatus. Ophthalmology 105, 448-457. 10.1016/S0161-6420(98)93026-3 - DOI - PubMed
    1. Bambakidis N. C. and Miller R. H. (2004). Transplantation of oligodendrocyte precursors and sonic hedgehog results in improved function and white matter sparing in the spinal cords of adult rats after contusion. Spine J. 4, 16-26. 10.1016/j.spinee.2003.07.004 - DOI - PubMed
    1. Biernaskie J., Sparling J. S., Liu J., Shannon C. P., Plemel J. R., Xie Y., Miller F. D. and Tetzlaff W. (2007). Skin-derived precursors generate myelinating Schwann cells that promote remyelination and functional recovery after contusion spinal cord injury. J. Neurosci. 27, 9545-9559. 10.1523/JNEUROSCI.1930-07.2007 - DOI - PMC - PubMed

Publication types

MeSH terms

LinkOut - more resources