Leukemia Cells Flash Fake Protein "ID" to Dupe the Immune System

A crucial protein on the surfaces of malignant cells shields them from destruction, but it could also provide a new way to attack cancer















Share on Tumblr

Limitations of an idea
The cell sorting technique, however, has limits, observes Douglas Smith, an oncologist and leukemia expert at Johns Hopkins University's Sidney Kimmel Comprehensive Cancer Center. He explains that "there have been many different attempts to find drugs or antibodies to 'purge' the leukemia from a patient's own bone marrow or blood cells so that they can be used in transplants. However, these approaches are not always effective. Most of the time, the patients own leukemia returns following the transplant."

According to Majeti, "we do not fully understand why the bone marrow starts making these abnormal cells in the first place"; predicting the return of leukemia is difficult. And Smith notes that "introducing stem cells from a donor for such a transplant avoids the risk of reintroducing the patient's own leukemia and is one reason transplants from donors have a better outcome for most leukemias."

Still, given the current poor understanding and prognosis of the disease, Smith goes on to say that the technique is an advance in how we study leukemia and normal blood cells. David Ritchie and Mark Smyth, both at the Peter MacCallum Cancer Center in Australia, are also optimistic about the implications of these papers. In a preview published in Cell, they wrote that these results will "ultimately lead to improved outcomes of leukemia."

The Stanford group believes that their findings will have implications regarding other cancers, as well. Irving Weissman, the senior author on the studies, suspects that CD47-based stealth might also play a role in other cancers. "I believe this will be a general mechanism for cancer to evade macrophages," he says, noting a 1992 study led by Ian Campbell that showed 90 percent of ovarian cancer cells express CD47 on the cell surface. The Stanford team is investigating the possibility that many cancerous cells use the CD47 protein as a shield.  And if they're right, new weapons can be developed that may target a wide range of cancers.



2 Comments

Add Comment
View
  1. 1. Liliana 07:59 AM 8/11/09

    Exploring CD47 protein in GoPubMed http://www.gopubmed.com/search?q=CD47

    Reply | Report Abuse | Link to this
  2. 2. rjsv30 08:35 AM 5/7/13

    CD47 is expressed on both blood stem cells and normal cells? The antibody would bind to both these cell types and mask the CD47 interaction with SIRP-alpha. What extent of normal cells would be then be subjected to phagocytosis by the macrophages? Does it fall under the safety level?

    Reply | Report Abuse | Link to this
Leave this field empty

Add a Comment

You must sign in or register as a ScientificAmerican.com member to submit a comment.
Click one of the buttons below to register using an existing Social Account.

More from Scientific American

See what we're tweeting about

Scientific American Editors

More »

Free Newsletters


Get the best from Scientific American in your inbox

Solve Innovation Challenges

Powered By: Innocentive

  SA Digital

Latest from SA Blog Network

  SA Digital

Science Jobs of the Week

Email this Article

Leukemia Cells Flash Fake Protein "ID" to Dupe the Immune System

X
Scientific American Magazine

Subscribe Today

Save 66% off the cover price and get a free gift!

Learn More >>

X

Please Log In

Forgot: Password

X

Account Linking

Welcome, . Do you have an existing ScientificAmerican.com account?

Yes, please link my existing account with for quick, secure access.



Forgot Password?

No, I would like to create a new account with my profile information.

Create Account
X

Report Abuse

Are you sure?

X

Institutional Access

It has been identified that the institution you are trying to access this article from has institutional site license access to Scientific American on nature.com. To access this article in its entirety through site license access, click below.

Site license access
X

Error

X

Share this Article

X