On the 27th of June 2015, it was reported that a Belgian woman had become the first to successfully conceive a child after having her ovarian tissue, which had been removed and frozen when she was thirteen due to sickle cell anaemia, transplanted back into her body.
Sickle cell anaemia is a genetic disorder which causes a base mutation on the coding strand of DNA in the genes that produce haemoglobin, which results in the deformation of red blood cells, making them become sickle shaped and unable to carry enough oxygen. The disorder can lead to fatal complications such as strokes, pulmonary hypertension and kidney dysfunction, which can lead to kidney failure.
Belgian doctors offered the woman in question a stem cell transplant from one of her siblings, at age eleven; however, the procedure involved intense chemotherapy in order to destroy the sickle cells, which would inevitably damage her ovaries and make her infertile. She chose to have fragments of her right ovary removed and frozen. Ten years on, these fragments were grafted onto her left ovary and two years later she conceived a boy. This has been considered a huge medical breakthrough for fertility, especially concerning young women with cancer. This story got me thinking about other critical fertility landmarks in the past decades and how they are affecting society today.
Test tube babies
On the 25th July, 1978, Louise Joy Brown, the first “test tube” baby was born. The baby was the product of the first In Vitro Fertilization (IVF) procedure, developed by gynaecologist Patrick Steptoe and physiologist Robert Edwards (the latter won the Nobel Prize for Medicine in 2010). The basis of the IVF used with Brown’s parents was the mother’s eggs collected from her fallopian tubes after her natural ovulation. The sperm was then fused with the egg outside the womb, dividing to form an embryo, which was then inserted into the uterus. The procedure, although following the same steps, has quickly developed to make it more likely that a foetus will develop and that many women in a high age range can become pregnant, by using techniques such as Transvaginal Oocyte Retrieval, which means many oocytes (immature egg cells can be removed), drugs for ovarian hyperstimulation which have the aim to produce 2-7 eggs which can form embryos and the injection of hormones such as progesterone in order to increase the success rate of implantation.
In 2013 it was estimated that over 5 million people have undergone IVF; however, the process doesn’t always work. According the NHS website the success rates are:
• 32.2% for women under 35
• 27.7% for women aged 35-37
• 20.8% for women aged 38-39
• 13.6% for women aged 40-42
• 5% for women aged 43-44
• 1.9% for women aged over 44
Also, there have been considerable ethical and social issues with the IVF procedure such as a religious view of “playing God” and life beginning with conception and so throwing away embryos not being implanted is murder. There are also medical risks such as multiple births when more than one embryo is transferred back into the uterus, which can lead to prematurity and pregnancy loss. Despite this, IVF has enabled millions of infertile couples be able to have children when previously it had been impossible, changing countless lives.
On the 24th of February of this year, the House of Lords passed an amendment to the 2008 Human Fertilisation and Embryology Act in order to allow a new and controversial IVF technique, the aim of which is to prevent children being born with serious mitochondrial diseases, by using two eggs and a sperm: i.e. two mothers and a father. The process works by the DNA being removed from the donor egg cell through a process called Maternal Spindle Transfer. The DNA from the mother’s egg cell is removed and then is inserted into the donor egg. The rest of the process is very similar to the above process of IVF where the egg is fused with the sperm and is inserted into the uterus. This process has been encouraged as it has shown that the hybrid egg can prevent the inheritance of mitochondrial diseases as the genetic information that codes for the faulty mitochondria from the mother is not inserted into the donor egg.
However, this new procedure has caused great controversy, with The Human Genetics Alert claiming that it will “inevitably lead to a future of “designer babies”.” There are also questions about the safety of the procedure as it has not undergone any clinical trials yet and has only been tested on primates, mice and human eggs that have not been implanted into a uterus. Despite this, this procedure has serious potential to allow women with genetic mitochondrial abnormalities to have children of their own.
Making babies without men (or women)