Mitochondrial replacement therapy

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Mitochondrial replacement therapy
Synonyms Mitochondrial donation
MeSH D000069321

Mitochondrial replacement (MRT, sometimes called mitochondrial donation) is the replacement of mitochondria in one or more cells to prevent or ameliorate disease. MRT originated as a special form of in vitro fertilisation in which the future baby's mitochondrial DNA comes from a third party. This technique is used in cases when mothers carry genes for mitochondrial diseases. It is a approved for use in the United Kingdom. A second use is to use autologous mitochondria to replace mitochondria in damaged tissue to restore the tissue to a functional state. It has been used in clinical research in the United states to treat cardiac-compromised newborns.

Medical uses[edit]

In vitro fertilisation[edit]

Mitochondrial replacement therapy has been used to prevent the transmission of mitochondrial diseases from mother to child; it could only be performed in clinics licensed by the UK's Human Fertilisation and Embryology Authority (HFEA), only for people individually approved the HFEA, for whom preimplantation genetic diagnosis is unlikely to be helpful, and only with informed consent that the risks and benefits are not well understood.[1]

Relevant mutations are found in about 0.5% of the population and disease affects around one in 5000 individuals (0.02%)—the percentage of people affected is much smaller because cells contain many mitochondria, only some of which carry mutations, and the number of mutated mitochondria need to reach a threshold in order to affect the entire cell, and many cells need to be affected for the person to show disease.[2]

The average number of births per year among women at risk for transmitting mtDNA disease is estimated to approximately 150 in the United Kingdom and 800 in the United States.[3]

Prior to the development of MRT, and in places where it is not legal or feasible, the reproductive options for women who are at risk for transmitting mtDNA disease and who want to prevent transmission were using an egg from another woman, adoption, or childlessness.[4]:45

Tissue function[edit]

Autologous mitochondria extracted from healthy tissue and supplied to damaged tissue has been used to treat cardiac-compromised newborns. Alternatives to the approach include use of an extracorporeal membrane oxygenator (ECMO) or tissue/organ transplantation.[5]

Techniques[edit]

In in vitro fertilization and involves removing eggs from a woman, removing sperm from a man, fertilizing the egg with the sperm, allowing the fertilized egg to form a blastocyst, and then implanting the blastocyst. MRT involves an additional egg from a third person, and manipulating both the recipient egg and the donor egg.

As of 2016 there were three MRT techniques: maternal spindle transfer (MST), pronuclear transfer (PNT), and more recently as of that date, polar body transfer (PBT).[4]:46–47

Diagram of the meiotic phases, showing how the chromosomes look in metaphase II

In MST, an oocyte is removed from the recipient, and when it is in the metaphase II stage of cell division, the spindle-chromosome complex is removed; some of cytoplasm comes with it, so some mitochondria are likely included. The spindle-chromosome complex is inserted into a donor oocyte from which the nucleus has already been removed. This egg is fertilized with sperm, and allowed to form a blastocyst, which can then be investigated with preimplantation genetic diagnosis to check for mitochondrial mutations, prior to being implanted in the recipient's uterus.[4]:47–48

In pronuclear transfer, an oocyte is removed from the recipient, and fertilized with sperm. The donor oocyte is fertilized with sperm from the same person. The male and female pronuclei are removed from each fertilized egg prior to their fusing, and the pronuclei from the recipient's fertilized egg are inserted into the fertilized egg from the donor. As with MST, a small amount of cytoplasm from the donor egg may be transferred, and as with MST, the fertilized egg is allowed to form a blastocyst, which can then be investigated with preimplantation genetic diagnosis to check for mitochondrial mutations, prior to being implanted in the recipient's uterus.[4]:50

The process of fertilization in the ovum of a mouse, showing pronuclei.

In polar body transfer, a polar body (a small cell with very little cytoplasm that is created when an egg cell divides) from the recipient is used in its entirety, instead of using nuclear material extracted from the recipient's normal egg; this can be used in either MST or PNT. This technique was first published in 2014 and as of 2015 it had not been consistently replicated, but is considered promising as there is a greatly reduced chance for transmitting mitochondria from the recipient because polar bodies contain very few mitochondria, and it does not involve extracting material from the recipient's egg.[6]

Diagram showing the creation of polar bodies.

Cytoplasmic transfer[edit]

Cytoplasmic transfer was originally developed in the 1980s in the course of basic research conducted with mice to study the role that parts of the cell outside of the nucleus played in embryonic development.[2] In this technique, cytoplasm including proteins, mRNA, mitochondria and other organelles, is taken from a donor egg, and injected into the recipient egg, resulting in a mixture of mitochondrial genetic material.[2] This technique started to be used in the late 1990s to "boost" the eggs of older women who wanted to conceive but were having problems and led to the birth of about 30 babies.[2] Concerns were raised that the mixture of genetic material and proteins could cause problems with respect to epigenetic clashes, or differences in the ability of the recipient and donor materials to effect the development process, or due to the injection of the donor material.[2] After three children born through the technique were found to have developmental disorders (2 cases of Turner's syndrome and one case of pervasive developmental disorder (an autism spectrum disorder), the FDA banned the procedure until a clinical trial could prove its safety.[2] As of 2015 that study had not been conducted, while the procedure was in use in other countries.[2]

A related approach uses autologous mitochondria taken from healthy tissue to replace the mitochondria in damaged tissue. Transfer techniques include direct injection into damaged tissue and injection into vessels that supply blood to the tissue.[5]

Risks[edit]

In vivo fertilisation via MRT involves preimplantation genetic screening of the mother, preimplantation genetic diagnosis after the egg is fertilized, and in vitro fertilization. It has all the risks of those procedures.[4]:60

In addition, both procedures used in MRT entail their own risks. On one level, the procedures physically disrupt two oocytes, removing nuclear genetic material from the recipient egg or fertilized egg, and inserting the nuclear genetic material into the donor unfertilized or fertilized egg; the manipulations for both procedures may cause various forms of damage that were not well understood as of 2016.[7]:23

Maternal mitochondria will be carried over to the donor egg; as of 2016 it was estimated that using techniques current in the UK, maternal mitochondria will comprise only around 2% or less of mitochondria in the resulting egg, a level that was considered safe by the HFEA and within the limits of mitochondrial variation that most people have.[7]:23–24

Because MRT procedures involve actions at precise times during egg development and fertilization, and involves manipulating eggs, there is a risk that eggs may mature abnormally or that fertilization may happen abnormally; as of 2016 the HFEA judged that laboratory techniques in the UK had been well enough developed to manage these risks to proceed cautiously with making MRT available.[7]:33–34

Because mitochondria in the final egg will come from a third party, different from the two parties whose DNA is in the nucleus, and because nuclear DNA codes for genes that make some of the proteins and mRNA used by mitochondria, there is a theoretical risk of adverse "mito-nuclear" interactions. While this theoretical risk could possibly be managed by attempting to match the haplotype of the donor and the recipient, as of 2016 there was no evidence that was an actual risk.[7]:34–37

Finally, there is a risk of epigenetic modification to DNA in the nucleus and mitochondria, caused by the procedure itself, or by mito-nuclear interactions. As of 2016 these risks appeared to be minimal but were being monitored by long-term study of children born from the procedure.[7]:38

History[edit]

In the United States in 1996 embryologist Jacques Cohen and others at the Institute for Reproductive Medicine and Science, Saint Barnabas Medical Center in Livingston, New Jersey first used cytoplasmic transfer in a human assisted reproduction procedure.[8] In 1997 the first baby was born using this procedure (Emma Ott). In 2001, Cohen and others reported that 10 single babies, twins, and a quadruplet at his New Jersey clinic and a further six children in Israel had been born using his technique. Using modifications of his procedure, a baby had been born at Eastern Virginia Medical School, five children at the Lee Women's Hospital Infertility Clinic in Taichung, Taiwan.[9] twins in Naples, Italy[10] and a twins in India.[11] In total as of 2016, 30-50 children worldwide had been reported to have been born using cytoplasmic transfer.[12]

In 2002, the US Food and Drug Administration (FDA) asked a Biological Response Modifiers Advisory Committee Meeting to advise on the technique of cytoplasmic transfer to Treat Infertility. This committee felt that there were risks at the time of inadvertent transfer of chromosomes and enhanced survival of abnormal embryos.[12] The FDA informed clinics that they considered the cytoplasmic transfer technique as a new treatment, and, as such, it would require an Investigational New Drug (IND) application. Cohen's clinic started the pre-IND application but the clinic then went private, funding for the application dried up, the application was abandoned, the research team disbanded,[13] and the cytoplasmic transfer procedure fell out of favor.[14] In 2016, 12 (out of the 13) parents of children born using cytoplasmic transfer at the Saint Barnabas Center participated in a limited follow-up inquiry via online questionnaire. Children whose ages then were 13-18 reported no major problems.[15]

In 2009, a team in Japan published studies of mitochondrial donation.[16] In the same year, a team led by scientists at Oregon Health & Science University published results of mitochondrial donation in monkeys; that team published an update reporting on the health of the monkeys born with the technique, as well as further work it had done on human embryos.[17]

Human trials in oocytes in 2010 by Craven, et al. were successful in reducing transmission of mutated mtDNA. The results of the study found the mean tDNA carryover to stay under 2% in all of the experimental embryos. This was true for both the MI-SCC and PN transfer methods of MTR. This research did not extend past the blastocyst stage because of ethical concerns, but there are still concerns about whether or not results retrieved from the blastocyst stage are viable representations of whole embryos. Because of these speculations and to further the viability of MTR as a safe and effective technique, further research and clinical trials need to be initiated in order to test the efficacy of MTR in the long term in human patients.[18]

In the United Kingdom, following animal experiments and the recommendations of a government commissioned expert committee,[19] the Human Fertilisation and Embryology (Research Purposes) Regulations were passed in 2001 regulating and allowing research into human embryos. In 2004, the Newcastle University applied for a licence to develop pronuclear transfer to avoid the transmission of mitochondrial diseases,[20] and was granted the license in 2005. Following further research by Newcastle and the Wellcome Trust,[21][22] scientific review,[23] public consultations, and debate, the UK government recommended that mitochondrial donation be legalized in 2013.[24] In 2015 parliament passed the Human Fertilisation and Embryology (Mitochondrial Donation) Regulations, which came into force on 29 October 2015, making human mitochondrial donation legal in the UK. The Human Fertilisation and Embryology Authority (HFEA) was authorized to licence and regulate medical centers which wanted to use human mitochondrial donation.[25][26] In February 2016, the US National Academy of Sciences issued a report describing technologies then current and the surrounding ethical issues.[4]

The HFEA Safety Committee issued its fourth report in November 2016 recommending procedures under which HFEA should authorize MRT,[7] the HFEA issued their regulations in December 2016[26][1] and granted their first licence (to Newcastle University) in March 2017.[27] On 6 February 2018, two women in the UK carrying mitochondrial DNA mutations were granted licences to undergo MRT.[28]

Professor Douglass Turnbull, the driving force behind mitochondrial research at Newcastle University, was awarded a knighthood in 2016.[29][30]

In 2016, John Zhang and his team at New Hope Fertility Center in New York, USA used the spindle transfer technique to help a Jordanian woman to give birth to a baby boy in Mexico where there was no law against using such a technique. The mother had Leigh disease and already had four miscarriages and two children who had died of the disease.[31] Valery Zukin, director of the Nadiya clinic of reproductive medicine in Kiev, Ukraine, reported in June 2018 that doctors there had used the pronuclear transfer method of MRT to help four women give birth (three boys and a girl), three women to become pregnant (one from Sweden) and had 14 failed attempts.[32] The doctors first got approval from an ethical committee and a review board of the Ukrainian Association of Reproductive Medicine[33][34] and the Ukrainian Postgraduate Medical Academy, under the auspices of the Ukrainian Ministry of Healthcare,[32] but there was no law in the Ukraine against MRT. One of the first children, a boy, was born to the 34-year-old woman in January 2017 and genetic test results were reported as normal.[35][36] In August and October 2017 the British HFEA authorised MRT for two women who had a genetic mutation in their mitichondria that causes myoclonic epilepsy with ragged red fibers.[37]

In August 2017, in a letter to Darwin Life, Inc. and New Hope Fertility Center, the FDA warned that the technique should not be marketed in the U.S.[38]

In June 2018 Australian Senate's Senate Community Affairs References Committee recommended a move towards legalising MRT and in July 2018 the Australian senate endorsed it.[39] Research and clinical applications of MRT were overseen by laws made by federal and state governments. State laws were, for the most part, consistent with federal law. In all states, legislation prohibited the use of MRT techniques in the clinic, and except for Western Australia, research on a limited range of MRT was permissible up to day 14 of embryo development, subject to a license being granted. In 2010, the Hon. Mark Butler MP, then Federal Minister for Mental Health and Ageing, had appointed an independent committee to review the two relevant acts: the Prohibition of Human Cloning for Reproduction Act 2002 and the Research Involving Human Embryos Act 2002. The committee’s report, released in July 2011, recommended the existing legislation remain unchanged.[40] Singapore was also considering whether to permit the MRT in 2018.[41]

In 2018, researchers announced the use of MRT to restore function to heart tissue in cardiac-compromised newborns. The damaged heart cells absorbed mitochondria extracted from healthy tissue and returned to useful activity.[5]

Society and culture[edit]

Regulation[edit]

As of February 2016, the United States had no regulations governing mitochondrial donation, and Congress barred the FDA from evaluating any applications that involve implanting modified embryos into a woman.[42]

The United Kingdom became the first country to legalize the procedure; the UK's chief medical officer recommended it be legalized in 2013;[24] parliament passed The Human Fertilisation and Embryology (Mitochondrial Donation) Regulations in 2015,[43][44] and the regulatory authority published regulations in 2016.[26]

Ethics[edit]

Despite the promising outcomes of the two techniques, pronuclear transfer and spindle transfer, mitochondrial gene replacement raises ethical and social concerns.[45]

Mitochondrial donation involves modification of the germline, and hence such modifications would be passed on to subsequent generations.[46] Using human embryos for in vitro research is also controversial, as embryos are created specifically for research and the financial compensation of egg donors.[47]

Implications for identity is another ethical concern with psychological and emotional impacts on a child's life regarding of a person's sense of identity. It debates whether the genetic make-up of children born as a result of mitochondrial replacement affect their emotional well-being when they are aware that they are different from other healthy children conceived from two parents.[48]

Opponents argue that scientists are "playing God" and that children with three genetic parents may suffer both psychological and physical damage.[49]

On the other hand, New York University researcher James Grifo, a critic of the American ban, has argued that society "would never have made the advances in treating infertility that we have if these bans had been imposed 10 years" earlier.[50]

On February 3, 2016, a report was issued by the Institute of Medicine of the National Academies of Sciences, Engineering, and Medicine (commissioned by the U.S. Food and Drug Administration) addressing whether it is ethically permissible for clinical research into mitochondrial replacement techniques (MRT) to continue. The report, titled Mitochondrial Replacement Techniques: Ethical, Social, and Policy Considerations analyzes multiple facets of the arguments surrounding MRT and concludes that it is 'ethically permissible' to continue clinical investigations of MRT, so long as certain conditions are met. They recommended that initially it should only be used for male embryos to ensure that DNA with mitochondrial disease would not be passed on.[4]

References[edit]

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