Charlie Gard would have turned one year old tomorrow.
The day before the British infant died of a mitochondrial disease on July 27, a short article inMIT Technology Reviewteased that Shoukhrat Mtalipov and his team at Oregon Health & Science University and colleagues had used CRISPR-Cas9 to replace a mutation in human embryos, a titillating heads-up that didnt actually name the gene or disease.
Yesterday Naturepublished the details of what the researchers call gene correction, not editing, because it uses natural DNA repair. I covered the news conference, with a bit of perspective, forGenetic Literacy Project.
Might gene editing enable Charlies parents, who might themselves develop mild symptoms as they age, to have another child free of the familys disease? Could anything have saved the baby?
A TRAGIC CASE
The court hearing testimonyon the case between Great Ormond Street Hospital (GOSH) and the family, published April 11, chronicles the sad story. The hospital had requested discontinuing life support based on the lack of tested treatment.
Charlie was born August 4, 2016, at full term and of a good weight, but by a few weeks of age, his parents noticed that he could no longer lift his head nor support any part of his body. By the October 2 pediatrician visit, Charlie hadnt gained any weight, despite frequent breastfeeding. After an MRI and EEG, Charlie had a nasogastric tube inserted to introduce high-caloric nutrition.
By October 11, the baby was lethargic, his breathing shallow. So his parents, Connie Yates and Chris Gard, took him to GOSH. There, physicians noted Charlies persistently elevated lactate. It was an ominous sign.
Remember Bio 101? When cellular respiration in the mitochondria fails, an alternate pathway releases lactic acid this is what causes muscle cramps in a sprinter right after a race. Its what was happening to the thousands of mitochondria in Charlies muscle cells; they werent extracting enough ATP energy from digested nutrients, and so the baby was limp, unable to reach or react much. His brain was running out of energy too.
On October 25, a muscle biopsy indicated only 6% of the normal amount of mitochondrial DNA, well below the 35% that indicates a mitochondrial DNA depletion syndrome (MDDS). But which one did Charlie have? Which gene was mutant? Thats important. With a judge discussing strains of the syndrome, as if it is a bacterial infection and not a monogenic disease, confusion loomed.
In mid November, sequencing of Charlies genome found two mutations in the gene RRM2B, causing infantile onset encephalomyopathic MDDS. It affected the brain and muscles that was obvious but he was also deaf and had heart and kidney abnormalities. With these findings, the Ethics Committee at GOSH advised against a ventilator.
Charlies disease is a block to the machinery in charge of supplying nucleotide building blocks for mitochondrial DNA synthesis, Fernando Scaglia, professor of medical and human genetics at Baylor College of Medicine, told me when I picked his brain on whether gene editing might help Charlies parents.
(A quasi-technical aside: RRM2B encodes an enzyme [ribonucleotide reductase] that, with three other subunits, removes an oxygen from the sugar part of nucleic acid building blocks, leaving deoxyribose as the sugar rather than ribose, with two phosphates attached. This happens just outside the mitochondria. Once these precursors get into the mitochondria, a third phosphate is added, forming the DNA nucleotide building blocks of the 37 mitochondrial genes. Charlie inherited a RRM2B mutation from each parent the gene is in the nucleus, but it is essential to supply the mitochondria with nucleotides. RRM2Bs enzyme works only in cells that arent dividing hence the extreme effects on Charlies muscles and brain.)
Charlies seizures started on December 15 and never let up. Experts began weighing in, including by the end of the month Michio Hirano from Columbia University, who had experience using nucleoside bypass therapy on 18 patients with MDDS due to mutations in a different gene, TK2. A ray of hope?
Nucleoside bypass therapy provides precursors to the DNA building blocks that have only one of the three phosphates, to circumvent the disabled enzyme, and because the full forms are too highly charged to easily enter cells. But the paper analyzingthe strategy, from 2012, clearly showed that it didnt work in an experimental system for Charlies disease myotubes, bits of non-dividing muscle in a dish:
First we suggest that not only myotubes (post-mitotic cells), but also myoblasts and possibly other dividing cells can show mtDNA depletion in RRM2B deficiency. Second, supplementation with dNMPs, as expected, had no beneficial effect in RRM2B deficiency. Based on the function of this protein supplementation with dNDPs could be tried as an alternative strategy in RRM2B deficiency. (This isnt a sentence, albeit the crucial one for the case; it means trying two phosphates instead of one.)
Im guessing that these three sentences are what catalyzed the parents GoFundMeeffort and desire to take their baby to the US. But theres never been a proper clinical trial for nucleoside therapy, said Dr. Scaglia, although 18 patients in Spain and Italy with mutations in a different gene, TK2, have so far tolerated it. But that form only affects muscle. The treatment might not have crossed the blood-brain barrier to reach Charlies more extensive disease.
Justice Francis knew the limitations of what some in the media called the pioneering treatment, if not the difference between a microbe and a gene. In fact, this type of treatment has not even reached the experimental stage on mice let alone been tried on humans with this particular strain of MDDS, he wrote.
From January 9th until the 27th, Charlie had an unrelenting storm of seizures, his EEG erratic even when he wasnt obviously seizing. This setback caused postponement of an ethics committee meeting and all but Dr. Hirano to give up. Perhaps he thought it a theoretical possibility because of that one sentence in the 2012 paper that suggested giving DNA precursors with 2 phosphates instead of one.
For a time, Columbia University considered treating Charlie, with what I dont know. Meanwhile, nurses noted and then testified that the baby was gaining weight but making no obvious progress, countering the parents observations that Charlie felt pain, distress, pleasure, and subtly communicated with them.
Then an EEG from March 30 convinced even Dr. Hirano that an attempt at any treatment would be futile a term that so dominated the court hearing that Justice Francis defined it: for the avoidance of any doubt, the word futile in this context means pointless or of no effective benefit.Goals began to focus on preventing suffering.
Yet the Pope and the Presidentweighed in circa July 4, offering to welcome the baby for unspecified treatment to the Vatican or US. What did they know that the English doctors didnt? And I had to wonder, where are these notables when similar things happen to many other babies born with rare genetic diseases? (See No Ice Buckets or Pink Ribbons for Very Rare Genetic Diseases)
For a time, discussion at the hearing devolved into a UK vs US scenario of the Brits taking a more reasoned approach in denying a futile therapy whereas US docs would try anything if parents could just raise enough money. The single-payer system in the UK was a factor too.
As the Pope and President were making their kind offers, pretty much all the experts were reaching agreement that Charlie should be taken off life support. Still, and understandably, the parents grabbed at any hope. We truly believe that these medicines will work, the father told the court, although nucleoside bypass was more an untested hypothesis than a medicine. Belief cant alter biochemistry.
And so Charlie passed away on July 27.
COULD ANYTHING HAVED SAVED CHARLIE?
It was too soon for nucleoside bypass therapy, nor were approaches for other mitochondrial diseases such as cofactor supplementation (which I wrote abouthere), liver transplant, or stem cell transplant applicable. Nor can a recently-described peptide-like moleculethat silences mitochondrial genes help, because Charlies mutant genes are in the nucleus. (A mitochondrion only houses 37 genes.)
Gene therapy or gene editing couldnt have saved Charlie, because the intervention would have to have infiltrated his many muscle and brain cells, damaged beyond repair. But could either approach enable his parents to avoid having another child with two doses of the RRM2B mutation? (Gene therapy introduces a functioning copy of a gene; gene editing can replace it.)
Couples who are carriers of the same recessive condition already have options to avoid passing on the disease: prenatal genetic testing to identify an affected fetus and ending the pregnancy, or preimplantation genetic diagnosis (PGD) following IVF and selecting healthy embryos to continue development in the uterus.
Unfortunately, yesterdays Nature paper about gene correction of a heart condition doesnt apply to Charlies family. The researchers used CRISPR-Cas9 to snip a dominant mutation from sperm at the brink of fertilizing an egg, jumpstarting a natural DNA repair mechanism that copies a normal version of the gene from the egg to reconstitute two functioning copies a little like me giving my husband a Womens March tee-shirt to match mine and replace his Jets tee-shirt. The approach wouldnt work for a sperm and an egg each bearing a recessive mutation in the same gene, the scenario for Charlie and 1 in 4 of his potential siblings, because there wouldnt be a healthy gene to copy.
Its easier to do PGD and select those embryos that would not have a mutation in the particular gene, as is done for many other conditions, Dr. Scaglia said. However, editing-out mutations can potentially help older women undergoing PGD by upping the percentage of okay embryos both the number of eggs and their quality decline precipitously with age. A more pressing problem, Dr. Scaglia added, is controlling the cost of PGD and getting insurance to cover it, rather than pursuing gene editing.
DID LIMITED UNDERSTANDING OF GENETICS PROLONG CHARLIES SUFFERING?
How should Charlie Gard have been treated? Given my experience as a hospice volunteer and cat owner, plus my knowledge of genetics and the pathways of cellular respiration, I think that he should have been taken off life support, which began in October, and given only love and palliative care, as soon as his mutation was identified from genome sequencing in November.
Sometimes we are kinder to our pets than we are to people.
In May I had to ask the vet to help my cat Panda cross the rainbow bridge. Panda had been losing weight for months, his kidneys failing. I knew the end was near when on a Sunday night he wandered to a spot in the garden where hed never gone before, curled up under a shrub, and stayed there. Cats do this. The next morning I took him to the vet for hydration and further treatment, and he had to stay there. But by Wednesday morning, when Panda backed into the cave of his cage even for me, I knew he was ready, even if I wasnt.
The kind vet gently added a barbiturate to Pandas IV. I didnt have to pull the plug on an invasive medical device, as had to happen for little Charlie. But I held tightly onto my kitty as life left him.
It was the right thing to do.
Here is the original post:
Charlie Gard Post-Mortem: Could He Have Been Saved? - PLoS Blogs (blog)
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