Select your localized edition:

Close ×

More Ways to Connect

Discover one of our 28 local entrepreneurial communities »

Be the first to know as we launch in new countries and markets around the globe.

Interested in bringing MIT Technology Review to your local market?

MIT Technology ReviewMIT Technology Review - logo


Unsupported browser: Your browser does not meet modern web standards. See how it scores »

{ action.text }

“Using these cells to find out which drugs work on an individual’s cells based on their genetics is a very promising new technology,” says geneticist Leroy Hood of the Institute for Systems Biology in Seattle, “though we have yet to see how promising.”

The cells provided by CDI also offer a ready supply for scientists conducting basic research in how cardiac cells function. But they do not come cheap. Palay says they cost about $1,000 for a vial, compared to about $800 for cells from cadavers, though the latter are not as readily available, and they don’t beat in a petri dish, limiting researchers’ ability to study the electrodynamics of heart cells.

IPS-derived cells also have the potential to become a powerful predictive tool when combined with genetic profiling that identifies genetic predispositions to adverse reactions to drugs. Cells derived from people with DNA markers giving them a high risk for side effects from a drug can be tested to determine if the risk is real before they ever take the medication.

“Before CDI, these cells were very difficult to obtain, and we would only get tiny amounts,” says stem cell biologist Sandra Engle, a senior principal scientist at Pfizer. “This doesn’t work for high-throughput testing for drugs.” Researchers use high throughput processes to test up to thousands of different drug compound candidates to see which work and are safe.

The cells also allow researchers to test cells from the same stem-cell stock over time as they develop drugs, which can take years, explains Engle. “We could not do that before.” Researchers also can check drugs on cells from different types of patients to see if there are different reactions, and study why some cells become diseased.

IPS cells are genetically and immunologically compatible with the person who provided the original cells. This means that cardiac and other cells produced from IPS cells won’t be rejected by a person’s immune system, always a possibility with cells that come from donors, animals, or cadavers.

Because of this, IPS-derived cells for the heart and other tissue may one day be a perfect genetic match for effecting repairs to damaged tissue in the heart and elsewhere, though IPS-derived cells cannot yet be used as spare parts. “Therapies using these cells are still a long way to go,” says Palay. “We don’t know yet know how to graft them to grow in human tissue.”

However, personalized drug testing has the potential to become a powerful predictive tool combining genetic profiling with cell-toxicity screening. It could help determine adverse reactions to drugs in genetically high-risk individuals before they ever take a given drug.

“This is a game changer,” says Engle.”It’s going to dramatically change biology and drug development.”

1 comment. Share your thoughts »

Credit: Cellular Dynamics International
Video by Cellular Dynamics

Tagged: Biomedicine, personalized medicine, heart, drug development, stem cell science, Cellular Dynamics International, drug testing

Reprints and Permissions | Send feedback to the editor

From the Archives


Introducing MIT Technology Review Insider.

Already a Magazine subscriber?

You're automatically an Insider. It's easy to activate or upgrade your account.

Activate Your Account

Become an Insider

It's the new way to subscribe. Get even more of the tech news, research, and discoveries you crave.

Sign Up

Learn More

Find out why MIT Technology Review Insider is for you and explore your options.

Show Me