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Legislative Alert on Stem Cell Research

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7/18/04
SENATE SUBCOMMITTEE ON SCIENCE, TECHNOLOGY, AND SPACE HOLDS HEARING ON ADULT STEM CELL RESEARCH

The Senate subcommittee on Science, Technology, and Space held a hearing on 14 July 2004 to assess recent progress made on adult stem cell research. Subcommittee chairman Senator Sam Brownback (R-KA), a leading opponent of embryonic stem cell research, sought to draw attention to adult stem cells as opposed to embryonic stem cells in order to publicize progress being made by "non-controversial techniques," and by unspoken implication, downplay the need for embryonic stem cell research. Subcommittee Democrats pointed out the limitations of adult stem cell research and used the hearing as a platform to criticize President Bush's limitations on embryonic stem cell research.

Clinical researchers and their patients presented testimony on successful therapies using adult stem cells. Dr. Michel Levesque of the Cedars-Sinai Medical Center in Los Angeles said that his therapy eliminated a patient's Parkinson's disease symptoms on the side of the body that was treated. In this therapy, Dr. Levesque extracted neural stem cells from the patient's brain, grew them in culture, and injected them into the area of the brain that had degenerated because of Parkinson's disease to replace the dead tissue. Similarly, Dr. Jean Peduzzi-Nelson of the University of Alabama at Birmingham testified that her studies in rats show that spinal cord injuries can be healed to an unprecedented extent by transplanting stem cells into the site of injury from the injured animal's own olfactory mucosa, a tissue lining the inside of the nose. Dr. Peduzzi-Nelson said her colleague, Dr. Carlos Lima in Lisbon, Portugal, has tested this therapy on several human patients, including three Americans. Two of these patients testified at the hearing. Both had been paralyzed as a result of spinal cord injuries for more than two years, but after the transplantation they are now able to walk with braces. Dr. Peduzzi-Nelson remarked that this improvement was better than she had ever observed.

However, these success stories may not be universally replicable. Dr. Robert Goldstein of the Juvenile Diabetes Research Foundation testified that adult stem cell therapy does not work to treat Type I diabetes, in which the pancreatic cells that produce insulin are destroyed. These insulin-producing cells are normally replenished by division, not differentiation from stem cells, so in a Type I diabetic, there is no source of adult stem cells within the patient's body that could replace the insulin-producing cells. He said JDRF's strategy is to fund both adult and embryonic stem cell research in the hope that something will provide a cure.

Despite Sen. Brownback's attempt to focus on adult stem cell research, subcommittee Democrats turned the spotlight on the controversy over embryonic stem cell research. Much of the debate centered on the limitations of adult v. embryonic stem cells for therapeutic purposes. Ranking minority member Ron Wyden (D-OR) cited NIH official statements that, compared to embryonic stem cells, adult stem cells are 1) not totipotent, 2) often present only in minute quantities, 3) perhaps not as capable of multiplying, and 4) more likely to have DNA or other damage. He argued that given these limitations, President Bush should remove the current restrictions on embryonic stem cell research because it may hold more promise for life-saving cures. Dr. Levesque acknowledged that adult stem cells are hard to isolate, but Dr. Peduzzi-Nelson testified that often only minute quantities of stem cells are required for effective therapy, and slow growth in adult stem cells is advantageous because it is more controlled than growth in embryonic stem cells. Drs. Peduzzi-Nelson and Levesque also pointed out that adult stem cells have the advantage that they will not cause immune rejection because they come from the patient's own body. Furthermore, they said, embryonic stem cells can form tumors when implanted.

However, pressed by Sen. Wyden, Dr. Levesque conceded that it is unknown whether embryonic stem cells will cause immune rejection, because there is not enough research on them due to President Bush's restrictions. Dr. Irving Weissman of Stanford University clarified that only undifferentiated embryonic stem cells tend to form tumors; differentiated embryonic stem cells do not. Dr. Weissman described one advantage of embryonic over adult stem cells: using somatic nuclear transfer (also known as cloning), researchers could create embryonic stem cell lines from individuals with genetic predispositions to develop disorders like juvenile diabetes and Lou Gehrig's disease. These cell lines would themselves develop the same disease in culture over time, providing a unique opportunity to study the molecular and genetic mechanisms of the disease. Dr. Peduzzi-Nelson used this point to suggest that the focus on embryonic stem cell research may be profit-driven. She argued that pharmaceutical companies want to remove President Bush's limits on embryonic stem cell research because embryonic stem cell lines (such as Dr. Weissman described) may be patented and become hugely profitable, while adult stem cell therapies such as hers and Dr. Lima's cannot be patented.

11/29/03

From the Society for Neuroscience

LEGISLATIVE ALERT: Contact Congress to Oppose Part of the Commerce-Justice-State Appropriations Bill That Would Hamper Stem Cell Research

The federal funding process is nearly complete and language to be included in a larger Appropriations bill would jeopardize stem cell research. The amendment, sponsored by Rep. Dave Weldon (R-FL), would forbid the U.S. Patent and Trademark Office (PTO) from granting patents on processes and products derived from embryonic stem cell research and therapeutic cloning (aka somatic cell nuclear transfer).

By prohibiting these patents, this amendment eliminates financial incentives for private companies to undertake this research. There are already government limits to federal funding for stem cell research. This amendment would create a disincentive for the private sector to move forward on such research, as well.