UK Parliament / Open data

Stem Cell Research

Proceeding contribution from Baroness D'Souza (Crossbench) in the House of Lords on Thursday, 3 May 2007. It occurred during Debate on Stem Cell Research.
My Lords, my thanks go to the noble Lord, Lord Patel, for introducing this debate, which is in large part about principles—whether existing medical and research techniques should conform to current ethical and moral norms in our society, or whether society should recognise the advances in medical science that are made every day and develop new standards to accommodatethose advances. There is, as lawyers point out, a fundamental rule in international law, especially that which governs human rights; customary law obliges states to adhere to standards that have been developed throughout the world—for example certain human rights abuses are subject to customary law and can never under any circumstances be condoned. Stem cell research in one of its aspects at least falls into this category of a widely accepted or customary practice. As we have heard, the UK is a global leader in stem cell research and there are centres throughout the world. Nowhere is this research better regulated than in this country, it would appear. The HFE Act 1990 is clear about what is allowed and what is not, and how research should be monitored. The point here is that stem cell research is an ongoing and major programme in the UK with many successes. Ethical and moral concerns will not cause it suddenly to cease but can guide its procedures as inevitably scientific progress comes up with new techniques to address human suffering. Where should the line be drawn? To assert categorically that it is impermissible to destroy embryos and/or to use animal cells to further this research is to ignore the long path, dating from the early 1970s when the first bone marrow transplant took place, of careful and diligent scientific inquiry and public debate thathas accompanied each stage. Earlier legislationhas allowed us to reach this stage, where radical techniques are now possible. The regulatory safeguards have been amended accordingly. Given that in vitro fertilisation has become almost standard practice, it has to be acknowledged that there will always be excess embryos which will be destroyed whether or not they are objects of research. I understand that, in the normal course of events, up to 30 per cent of fertilised embryos are lost before implantation by women who may not even be aware that they have conceived. It is neither logical nor necessarily ethical to be concerned with preserving excess embryos, especially if there is a strict time limit on their use. I ask your Lordships to consider whether it is moral to deny people access to medical techniques that already exist under stringent conditions. Would we be happy to do so if those we most loved faced degenerative conditions such as motor neurone disease, diabetes and/or dementia? Do we want to ignore the animal rights constituency and continue indefinitely with animal models when cellular ones may become more easily available? My final point concerns the use of embryos as well as of hybrids and chimeras in order to find alternative sources of cells. Much research is going on in these areas and a Stem Cell Bank with international links has already been set up, but needs far more investment to become a genuine alternative resource for medical science. For example, the challenges of safe, long-term storage, if met, could obviate the need for the future collection of embryonic stem cells. In the US, it is claimed that a case of sickle cell anaemia has been cured with transplanted cells harvested from umbilical cords. As I understand it, there is currently interest in amniotic fluid cells and autologous stem cells, which occur naturally in the body. The reprogramming of adult stem cells from brain, eyes, muscles and bone marrow is a fruitful area of research. All these procedures are waiting in the wings but need far more investment and far more research using embryonic and animal cells to become standard practice. The history of medical research is replete with accompanying ethical concerns—rightly so. However, these concerns have to be resolved through public debate, public engagement, transparency, regulation and monitoring, and this process is now taking place. The principle that I adhere to is the harvesting with humanity of stem cells, whatever their origin, thereby continuing what scientists are already doing in the interests of public good and an end to some kinds of human suffering.
Type
Proceeding contribution
Reference
691 c1184-5 
Session
2006-07
Chamber / Committee
House of Lords chamber
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