Proposals to forbid funds for cloning

hlichten

Super Moderator
I understand this and, of course agree with you. I have not read her book, but have pulled up reviews and synopsis of it.

For those that don't fully understand this, or are new to these conflicts, could you please list the "Readers Digest" version of this debate?
 

barbara

Pioneer Founding member
Public comments allowed

I will try to recap what I am reading to make it more "Reader's Digest". In the meantime, here is an article that explains it, although not quite in the Digest form. I posted this now however since comments from the public will be allowed.



The director of stem cell research at the Stanford University School of Medicine says he is troubled by draft guidelines issued today by the National Institutes of Health that would prohibit federal funding for research on stem cell lines created through a technique sometimes referred to as "therapeutic cloning" or somatic cell nuclear transfer.

Irving Weissman, MD, director of Stanford's Institute for Stem Cell Biology and Regenerative Medicine, said the SCNT technique is one way to create disease-specific human embryonic stem cell lines on which to conduct research and test therapies. He also took issue with the assertion that the NIH consulted existing guidelines from the National Academy of Sciences and the International Society for Stem Cell Research-both of which sanction the use of SCNT-derived cell lines-in coming up with its draft recommendations.

"Instead of facts, the NIH placed its own version of ethics in place of the president's clear proclamation," said Weissman, the Virginia & D.K. Ludwig Professor for Clinical Investigation in Cancer Research. "As head of the National Academy of Sciences' panel that unanimously endorsed research using SCNT, and as a drafter of the guidelines for the International Society for Stem Cell Research, I know that this suggested ban on federal funding of SCNT-derived human embryonic stem cell lines is against our policies and against President Obama's March 9 comments. The NIH has not served its president well."

On March 9, President Barack Obama signed an executive order removing previous restrictions on the use of federal funds for research on any human embryonic stem cell line derived after Aug. 9, 2001. He used the ceremony to remark that it is important to ensure "that scientific data is never distorted or concealed to serve a political agenda-and that we make scientific decisions based on facts, not ideology."

In announcing the draft guidelines, acting NIH director Raynard Kington, MD, PhD, justified the restriction in part by saying that there is a lack of scientific consensus as to the necessity of funding lines derived by SCNT and that, although the technique has been used to create many embryonic stem cell lines in animals, such human embryonic stem cell lines have not yet been documented.

"We believe there is strong, broad public and scientific support for the use of federal funds for research on cell lines from embryos derived through in vitro fertilization for reproductive purposes that would not otherwise be used," said Kington, noting that similar legislation had twice passed both the House and Senate only to be vetoed by former President George W. Bush. "We do not see similar broad support for using federal funding for research on cell lines from other sources."

The somatic cell nuclear transfer technique involves removing the nucleus from an egg cell and replacing it with a nucleus from a different cell in order to create an embryonic stem cell line genetically identical to the donor nucleus. In the case of a donor who suffers from a condition like Parkinson's disease, the SCNT process would yield an embryonic stem cell line that could be used to test specific therapies for that patient.

If the draft guidelines are adopted, they would underscore the continued need for the California Institute for Regenerative Medicine, which has funded grants to several scientists working to create specific human embryonic stem cell lines for research purposes. The institute was established in 2005 by Proposition 71 to counteract the effect of President Bush's limits on federal funding of such research.

"Methods like SCNT were specifically sanctioned by Prop. 71," said Geoff Lomax, PhD, the senior officer to the state institute's Standards Working Group, which was instituted to develop ethical guidelines for the use of embryos in CIRM-funded research. "These potential restrictions on the range of research materials available for federal funding ensure that CIRM will continue to play a unique role in the world of stem cell research."

"For certain types of research, CIRM could remain very important," concurred Renee Reijo Pera, PhD, director of Stanford's Center for Human Embryonic Stem Cell Research and Education. Reijo Pera said she had expected the NIH guidelines to be somewhat conservative, particularly where SCNT is concerned.

"I am happy that these are draft guidelines," said Weissman, who noted that the NIH did not solicit input from either the National Academy of Sciences or the International Society for Stem Cell Research during the consensus process. "I'd like to remind the NIH of the principles enunciated by the president on March 9. Research in this area is moving very fast, and it's not possible to say whether advances will come from work on adult-derived iPS cells or from embryonic stem cells created by nuclear transfer. Policy needs to be developed as the field develops, rather than precluding something based on ideology."

The proposed NIH guidelines will be available for public comment for 30 days, and the final guidelines will be released by the agency on or before July 7. They can be viewed at http://stemcells.nih.gov/policy/2009draft. Comments can be mailed, or submitted electronically after the guidelines are published in the Federal Register by April 24.

The Stanford University School of Medicine consistently ranks among the nation's top 10 medical schools, integrating research, medical education, patient care and community service.
 

barbara

Pioneer Founding member
More on the therapeutic cloning debate

I do hope the media makes the effort to thoroughly present this issue in a scientific vein rather than a political vein, but I am sure that is only wishful thinking. Cloning of human beings is outlawed in the bill and justifiably so and yet that does not seem to satisfy some who don't "trust" such language. I have a hard time understanding that type of reasoning to be perfectly honest. I believe it is an effort to stir up controversy where none needs to exist and in the end it will hinder scientists in their research. Here is the article:




Antiabortion-Rights Groups Oppose Draft Legislation Allowing Research Into Therapeutic Cloning

Article Date: 30 Apr 2009


The "next big biomedical research debate" in Congress could be about whether to allow federal funding of research into "somatic cell nuclear transfer," also known as therapeutic cloning, to produce stem cells, CQ Today reports. President Obama's executive order easing restrictions on federal funding for embryonic stem cell research directed NIH to determine guidelines for the research. The draft guidelines issued by NIH restrict federal funding to research involving embryonic stem cell lines derived from unused embryos created for fertility treatments and willingly donated by patients who have given written consent. NIH added that embryonic stem cells derived from other sources, including cloning, will not be eligible for federal funding.

According to CQ Today, Reps. Diana DeGette (D-Colo.) and Michael Castle (R-Del.) are working on draft legislation that would codify Obama's executive order and contain language allowing NIH to pursue research on SCNT. DeGette said that her draft legislation would not require NIH to fund SCNT but that it could encourage such research. "I hope the NIH will allow SCNT to move forward with federal funding," DeGette said, adding, "But if they don't do that right now, what our bill will do is allow them to change that in the future if research shows it is a necessity and can be done ethically." DeGette added that other Democratic representatives support her work. In addition, DeGette said her bill would contain language outlawing reproductive cloning, a technique that creates a genetic copy of a person.

According to CQ Today, many experts believe therapeutic cloning could lead to the development of new treatments such as tissue transplants that have no risk of rejection by a patient's immune system. However, antiabortion-rights groups contend that it could lead to the creation of what they call "human embryo farms" for the purpose of obtaining embryonic stem cells or enable "unscrupulous" scientists to bring a cloned embryo to term, CQ Today reports. The National Right to Life Committee last month sent a letter to Congress alleging that the draft DeGette-Castle bill could be a "'bait and switch'" by using ambiguous language to mask its intent to allow federal funding for cloned embryonic stem cells.

Sen. Tom Harkin (D-Iowa), sponsor of an embryonic stem cell research bill that former President George W. Bush vetoed in 2007, said he is comfortable with Obama's position on the subject. "Scientists will still be able to study SCNT using private funding," Harkin said, adding, "But it's important to note that no one has yet succeeded in creating a human stem cell line using SCNT. As yet, this is only a theoretical approach" (Wayne, CQ Today, 4/27).
 

barbara

Pioneer Founding member
NOt all trades are equal - an argument for therapeutic cloning research

Obama's bad stem cell compromise
Obama traded his word on stem cell research for a political deal, sacrificing 'therapeutic cloning' research necessary to help millions suffering from Alzheimer's, diabetes and other illnesses.
By Marion Roach
May 10, 2009
I just had a birthday, and to honor such occasions, my sister always gives me silver. Not just any silver: It's our parents' simple wedding flatware pattern, which Margaret collects for me, a piece at a time. Over the years that the slender boxes have appeared, I've wondered if any of it is from the full service for 12 that I pulled in a suitcase through Manhattan's Diamond District and sold one dreadful day 25 years ago.

It had been my assignment to sell it -- that, and a ring of Margaret's, one of mine and, right off our mother's finger, her engagement ring and platinum wedding band. The sum received was probably a quarter of their monetary worth, and nothing near their emotional value, but it financed two more weeks of home care for our mother, an Alzheimer's disease patient. After five years of caring for her at home, we had run through the family savings.


It was a few years before the sale of the silver that I first wrote about us, in a 1983 magazine article that, impossible as it may seem now, introduced Alzheimer's disease to millions of people who didn't know what it was, including the seasoned magazine editor to whom I first pitched the story. Tonight, HBO will begin a three-night series, produced by California's first lady, Maria Shriver, about a disease that now needs no introduction.

When I first wrote about Alzheimer's, I searched out some of the best minds of the time, including Lewis Thomas, the great science writer, former dean of Yale Medical School and then-chancellor of the Memorial Sloan-Kettering Cancer Center. He called Alzheimer's disease "the disease of the century" because, he said, "of all the health problems in the 20th century, this one is the worst."

That quote got people's attention, as did the words "angry, incompetent, hostile and incontinent," which is how I described my mother. She was then 51, two years younger than I am now. I exposed her for who she had become in exchange for the attention I hoped the article might bring for her disease.

In the months and years that followed, congressional hearings were held, state task forces were convened and city committees were formed. Research dollars were allotted as well. But those were the 1980s, when Ronald Reagan was president, and despite the fact that embryonic stem cell research had been conducted in the U.S. since the middle of the 20th century, contributing to such wonders as vaccines for both rubella and polio, it was rebranded and became strongly associated with abortion. In the years that followed, despite the well-known fact that stem cell research was the most promising path to finding cures for Alzheimer's, Parkinson's, diabetes, multiple sclerosis and other diseases, this country allowed the personal beliefs of the antiabortion forces to become public policy. And that lasted a very long time.

The great art of political compromise is a fundamental part of our representative government. Deals are made in which one side cashes in some influence in order to move something along. This is what apparently happened last month, and shortly afterward, White House spokesman Reid Cherlin announced that President Obama had "directed [the National Institutes of Health] to formulate the best method for moving forward with stem cell research, both ethically and scientifically."

In his grand exchange, the president traded away an essential piece of what he had only recently said he believed. When he campaigned, Obama said he supported the "therapeutic cloning of stem cells." But as president, he has already traded that position for one that some see as more politically realistic. Under the compromise plan, the president proposed that federal dollars be allowed to pay only for research on stem cell lines created from surplus fertility clinic embryos, but that funds continue to be barred from stem cell lines created in the laboratory to study particular diseases. Also barred is financial support for creating new, genetically matched stem cells for use in the treatment of disease. That is the very "therapeutic cloning" research that the president supported during his campaign.

After the president issued his executive order, many scientists shrugged; it was, they said, the compromise they'd expected.

I understand the value of a good trade, but I don't see what makes this one worthwhile. Every American, everybody everywhere, ought to support all possible efforts to find a cure for Alzheimer's disease. My mother was one of 4.5 million Americans with it; today there are 5.3 million, and by 2050, experts project 16 million American Alzheimer's patients, a surge that can be attributed partly to longer life spans and partly to increased diagnosis. Worldwide, 26.6 million people have it, with a mid-century surge expected to reach 100 million.

My family paid for home care with an exchange of goods; Medicaid paid for the next eight years of care in the nursing home, where my mother died at 64. Today, out-of-pocket costs for families caring for those with Alzheimer's and the other dementias are triple what they are for other illnesses, and the yearly cost to the U.S economy is now at $148 billion. Every 70 seconds, someone develops the disease.

Years ago, as my sister began giving me pieces of silver, there again were the long, flat knife handles that I had gently fingered during Thanksgiving dinners, the forks I balanced on the backs of my hands as my parents told stories, the spoons from which I had fed the dog under the table. There was a time when I thought that people were supposed to have silver and china and crystal, and I expected to have them, choosing them at the time of my own wedding. It seemed a tribal currency that was securely in the bank. Merely silver, perhaps, but to me it had been gold bullion, a representation of the standard below which you did not slip.

Then the situation changed, and the flatware would be counted among the least of our losses during that awful time.

Right now, the NIH is formulating the research guidelines for the new stem cell policy and has opened a 30-day public comment period.

Here are mine: Not all trades are equal. Sell your stuff? That's easy. But never hock your values. You can't get those back a piece at a time.

Marion Roach, who writes for thesisterproject.com, is based in

New York.
 
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