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Proceeding contribution from Mark Simmonds (Conservative) in the House of Commons on Monday, 12 May 2008. It occurred during Debate on bill on Human Fertilisation and Embryology Bill.


Human Fertilisation and Embryology Bill

This has been an excellent and stimulating debate, which has belied the concerns, rumours and accusations that the House could not cope with such complex issues. There have been contributions demonstrating real passion and real expertise. The contributions have been intelligent and well informed, particularly that of my hon. Friend the Member for South Cambridgeshire (Mr. Lansley), the shadow Secretary of State. The Bill is evolutionary and thought provoking, but the debate has demonstrated the significant diversity and disparity of views in the House, reflecting the diversity and disparity of views outside, although not necessarily in the same proportion. I have enormous respect for those with ethical and moral reservations about the Bill. As one who is married to a south American Catholic, I understand how deeply and passionately held those views are. The comments that I am about to make from the Dispatch Box are therefore my personal views, not necessarily those of the entire party that I represent. The 1990 Act has proved a robust piece of legislation. Credit for that must go to my right hon. and learned Friend the Member for Rushcliffe (Mr. Clarke) who, with his colleagues, piloted the Bill successfully through the House 18 years ago. The Act was also built on the excellent work of Baroness Warnock and her colleagues, whose ideas were its precursors. However, the 1990 Act should now be updated and reviewed, within an ethical framework, in the light of advances in science, medicine and technology. As other Members have said, Britain is a world leader in reproductive stem cell technologies. We should be proud of that heritage and want Britain to remain at the forefront of such scientific research, in a clear ethical framework. Britain has flourished in the field, not only because of the skills of our scientists and our first-class facilities but because of the clearly defined regulatory environment, grounded on ethical platforms. It is right that the complex issues involved should be carefully considered in Parliament and the country as a whole, and I welcome the national debate on many of the controversial and important issues. However, it is also right that Members should be able to vote with their consciences on these key moral issues. It was wrong of the Government to try to whip the Bill, as they originally intended, and it was wrong to whip the Bill in the other place. I am pleased that Conservative Members will have a free vote throughout the Bill's passage. In answering interventions from my right hon. and learned Friends the Members for Rushcliffe and for Devizes (Mr. Ancram), both distinguished and experienced Members, the Secretary of State gave no decent response on why Government Members would not get a completely free vote, which the House had in 1990. I suspect that if the Secretary of State and the Minister had their way, this would be a completely free vote for Government Members. There is a large number of controversial and complex aspects to the Bill and it is right that some of the votes should be on the Floor of the House; we Conservatives have been pressing for that. I am pleased that many more Members will have the opportunity to contribute to the debate. We believe that the programme motion is incorrect and that there should be longer debates, particularly on admix embryos. If we are to debate abortion as part of our discussion of the Bill, that should be for longer than three hours. The debate on schedule 2, which contains provisions on not only saviour siblings, but such important issues as embryo selection, embryo research and, potentially, the issue of birth certificates, will all be taken in a three-hour period next Tuesday afternoon if the programme motion goes through. That will not allow anything like the time that should be allocated for such significant issues. We will have time to debate in detail the four different types of admix embryos, but there are significant differences between them. I will not go through them in detail now, but I want to highlight one or two key differences. Cytoplasmic embryos are a mix of only up to 0.1 per cent. of the genetic material. Transgenic embryos probably usually transmit only one gene—but not gametes, which are sex cells—into animal mitochondria. Human-animal chimera embryos are useful for understanding how stem cells develop into the different types of cells in our bodies. However, the main issue during the debate on admix embryos will be the necessity or otherwise for true hybrids. Some hon. Members have said that they do not believe that there are disparities between the types of potential admix embryos, but there are. True hybrids are the only ones that are 50-50 and the only ones to merge the sex cells of animals and humans. We shall certainly table further amendments to enable further discussion on these important issues. There is a shortage of eggs, a point rightly articulated by my hon. Friend the Member for Buckingham (John Bercow). However, it must be understood that the animal eggs are used only as a vessel to ensure an ample supply of eggs for research. My hon. Friend the Member for Stone (Mr. Cash) and others have cited the work of Professor Yamanaka in Kyoto. Recently, I was fortunate enough to go to Kyoto university to discuss these issues with Professor Yamanaka's team, which does not want embryonic stem cell research to cease. In fact, it needs to have a laboratory in California, which has a more permissive regulatory regime than Japan, in order to carry out embryonic stem cell research and continue its work on pluripotent cells. Let me quote what it said when I asked what would happen if embryonic stem cell research was not allowed: ““We still need embryonic stem cells. If embryonic stem cells were not allowed we would be in trouble. Achievements here are based on former work done on embryonic stem cells.”” These issues are not mutually exclusive. The development of induced pluripotent cells is an excellent advance, but the process is not without problems. Many scientists are concerned about the risk of telomere degeneration in induced pluripotent cells, as well as mitochondrial degeneration, damage from the virus used to stimulate reproduction, and the risk of reintroducing defective genes, culminating in potentially significant tumour growth—a point correctly made by the hon. Member for Bolton, South-East (Dr. Iddon). I believe that all types of stem cell research—embryonic, adult and cord blood—must continue, as we do not know which, if any, will herald cures for some of the serious diseases that exist. However, I have reservations about true hybrids, to which we will return in Committee. Hon. Members rightly raised the issue of saviour siblings and embryo selection. The Bill is absolutely right to outlaw sex selection for non-medical reasons. However, pre-implantation genetic diagnosis—PGD—will be permitted if there is a significant risk of a child developing a serious gender-related physical or mental disability, serious illness or other serious medical condition. It is not compulsory for parents with possible genetic illnesses to use PGD, and rightly they may not use it to select any positive characteristics. The Bill also permits the selection of embryos in order to provide compatible cord blood cells, bone marrow or other tissue to a sibling with a serious medical condition. Cells are taken from the umbilical cord of the saviour sibling, and, as a very last resort, bone marrow. It is clearly very controversial, but the creation of a saviour sibling already occurs, if only rarely: to date, the HFEA has licensed tissue typing for only six families. It is, and should remain, a last resort. In that context, cord blood is known to be an excellent source of useful stem cells. As other hon. Members have pointed out, 98.5 per cent. of cord blood is currently thrown away. Retaining more would not entirely obviate the need for the creation of saviour siblings, but it would increase the chances of a match being found for a seriously ill child. I urge the Government to consider ways of increasing the amount of cord blood that is banked. Let me turn my attention to the so-called ““need for a father”” clause. The important thing is the welfare of the child. The hon. Member for Oxford, West and Abingdon (Dr. Harris) needs to be careful. We will have a great deal of debate throughout the passage of the Bill, and he must not assume that those who disagree with him start from a basis of prejudice—we do not. The Bill requires fertility clinics to take into account the need for a father when providing treatment. It is widely accepted that the clause has not stopped same-sex couples and single women facing barriers in accessing treatment, nor would it in future were it to remain. The hon. Member for Morecambe and Lunesdale (Geraldine Smith), who, sadly, is not in her place, rightly pointed out that there is no evidence to contradict this.


Secondary information

Type
Proceeding contribution
Reference
475 c1152-4 
Session
2007-08
Chamber / Committee
House of Commons chamber
Subjects
Civil partnerships Clones Abortion Blood Fertility Human embryo experiments Diseases Donors Genetics Human Fertilisation and Embryology Authority Ethics IVF Discrimination Foetal tissue NHS Medical treatments Screening Religion Sexuality Research Stem cells Christianity Human-animal hybrid embryos
Legislation
Human Fertilisation and Embryology Bill (HL) 2007-08
Link
View this Proceeding contribution on www.publications.parliament.uk