Oct. 4, 2013  A group of Brigham and  Women's Hospital, and Harvard Stem Cell Institute researchers,  and collaborators at MIT and Massachusetts General Hospital have  found a way to use stem cells as drug delivery vehicles.
    The researchers inserted modified strands of messenger RNA into    connective tissue stem cells -- called mesenchymal stem cells    -- which stimulated the cells to produce adhesive surface    proteins and secrete interleukin-10, an anti-inflammatory    molecule. When injected into the bloodstream of a mouse, these    modified human stem cells were able to target and stick to    sites of inflammation and release biological agents that    successfully reduced the swelling.  
    "If you think of a cell as a drug factory, what we're doing is    targeting cell-based, drug factories to damaged or diseased    tissues, where the cells can produce drugs at high enough    levels to have a therapeutic effect," said research leader    Jeffrey Karp, PhD, a Harvard Stem Cell Institute principal    faculty member and Associate Professor at the Brigham and    Women's Hospital, Harvard Medical School, and Affiliate faculty    at MIT.  
    Karp's proof of concept study, published in the journal    Blood, is drawing early interest from    biopharmaceutical companies for its potential to target    biological drugs to disease sites. While ranked as the top    sellers in the drug industry, biological drugs are still    challenging to use, and Karp's approach may improve their    clinical application as well as improve the historically mixed,    clinical trial results of mesenchymal stem cell-based    treatments.  
    Mesenchymal stem cells have become cell therapy researchers'    tool of choice because they can evade the immune system, and    thus are safe to use even if they are derived from another    person. To modify the cells with messenger RNA, the researchers    used the RNA delivery and cell programming technique that was    previously developed in the MIT laboratory of Mehmet Fatih    Yanik, PhD. This RNA technique to program cells is harmless, as    it does not modify the cells' genome, which can be a problem    when DNA is used (via viruses) to manipulate gene expression.  
    "This opens the door to thinking of messenger RNA transfection    of cell populations as next generation therapeutics in the    clinic, as they get around some of the delivery challenges that    have been encountered with biological agents," said Oren Levy,    PhD, co-lead author of the study and Instructor of Medicine in    Karp's lab. The study was also co-led by Weian Zhao, PhD, at    University of California, Irvine who was previously a    postdoctoral fellow in Karp's lab.  
    One such challenge with using mesenchymal stem cells is they    have a "hit-and-run" effect, since they are rapidly cleared    after entering the bloodstream, typically within a few hours or    days. The Harvard/MIT team demonstrated that rapid targeting of    the cells to the inflamed tissue produced a therapeutic effect    despite the cells being rapidly cleared. The scientists want to    extend cell lifespan even further and are experimenting with    how to use messenger RNA to make the stem cells produce    pro-survival factors.  
    "We're interested to explore the platform nature of this    approach and see what potential limitations it may have or how    far we can actually push it," Zhao said. "Potentially, we can    simultaneously deliver proteins that have synergistic    therapeutic impacts."  
See the article here:
Stem cells engineered to become targeted drug factories