Islet cell transplant trial outcome ‘major milestone' toward cure for diabetes
When Amanda Smith learned at the age of 25 that she had late-onset Type 1 diabetes, she considered the diagnosis a death sentence.
The nurse, from London, Ont., had a particularly dim view of the disease because she grew up watching her mother struggle with it. Her mother would slur her words and lose consciousness when her blood sugar bottomed out. Once, Ms. Smith's grandfather had to break a window to reach her mother, who was passed out in her home holding a banana she had tried to consume to raise her blood sugar.
'It literally eats you from the inside out,' said Ms. Smith, now 36. 'It rots your teeth, it destroys your body, your vision. The complications that come with Type 1 diabetes are so extreme.'
Ms. Smith is confident now that those complications won't be in her future. In February of 2023, she became the first Canadian to receive a transplant of islet cells – the cells in the pancreas that make insulin – derived from embryonic stem cells.
The transplant freed her from insulin and gave her blood sugar control akin to a non-diabetic. It was performed at Toronto General Hospital, the institution where insulin was first tested more than 100 years ago.
On Friday, the results of the clinical trial in which Ms. Smith participated were published in the New England Journal of Medicine. The early-phase trial was small, and the procedure has a significant downside in that patients must take anti-rejection drugs for life, just like recipients of organ transplants.
For people living with diabetes, the push for medical coverage isn't political, it's personal
Nonetheless, the study's outcome counts as 'spectacular,' according to James Shapiro, who holds the Canada Research Chair in transplant surgery and regenerative medicine at the University of Alberta and was not involved in the study. Ten of the 12 participants who received a full dose of the cells were insulin-independent one year later.
'This is a major advance and a major milestone along the journey towards a cure,' he said.
Dr. Shapiro was himself responsible for an earlier breakthrough on that path. In 2000, he and his colleagues at the University of Alberta published a seminal paper on a method they developed for safely and effectively transplanting islet cells from deceased donors into patients with Type 1 diabetes. They dubbed their regimen the 'Edmonton Protocol.'
'We used to call it the drive-through transplant,' Dr. Shapiro said, because giving patients islet cells was less risky and burdensome than a whole pancreas transplant. The cells are infused into patients under mild sedation with an IV-drip into the portal vein of the liver.
The breakthrough described in the new paper is that the islet cells transplanted into Ms. Smith were derived not from deceased donors but from embryonic stem cells, which function as a type of source code that scientists can coax into becoming any cell in the human body.
The supply of such lab-created islets could, in theory, be limitless, unlike the supply of deceased donor islets.
Semaglutide, or Ozempic, reduces symptoms of feared diabetes' complication, study finds
Trevor Reichman, director of the pancreas and islet transplant program at the University Health Network's Ajmera Transplant Centre, said the most encouraging result is that the islet-cell transplants eliminated dangerous blood sugar 'lows' that can cause confusion, seizures and unconsciousness. He ran the study site at UHN and is an author of the new paper.
'All of them, essentially, were able to get rid of their hypoglycemic episodes,' Dr. Reichman said, 'so all of the real risks to them, all of the lows, were essentially eliminated.'
Still, the international trial, funded by Boston-based Vertex Pharmaceuticals, wasn't without its challenges.
The company paused it temporarily last year after two participants died, though not from taking Zimislecel, the brand name of the new islet therapy. Vertex expects to apply for regulatory approval of Zimislecel starting next year.
One participant died of severe dementia 30 months after the infusion. That patient had pre-existing neurocognitive impairment and, before joining the trial, had suffered a brain injury during a motor-vehicle accident caused by a severe blood sugar low.
The other died of cryptococcal meningitis, a fungal infection caused by a sinus surgery. The death was related to the immunosuppressant medication that the participant was taking to preserve the islet transplant, the study said.
That death underscores the tradeoff that people with Type 1 diabetes would have to make with Zimislecel, said Rémi Rabasa-Lhoret, director of the Metabolic Diseases Research Unit and The Diabetes Clinic at the Montreal Clinical Research Institute.
He wonders how many people with Type 1 would be willing to take anti-rejection drugs for life, especially now that advances such as insulin pumps have made diabetes easier to manage for some patients.
'It's probably going to be a very narrow population,' Dr. Rabasa-Lhoret said.
The next step for scientists is finding a way to genetically engineer or encapsulate islets so the immune system won't view them as hostile invaders.
In the meantime, Ms. Smith said taking three pills, three times a day to suppress her immune system is a breeze compared with the round-the-clock work of keeping her blood sugar in check.
Her 10-year-old daughter, Draya, used to say she wanted to become a doctor to cure diabetes. Now, she talks of being a pilot or engineer.
'I would do this a million times over compared to the maintenance I used to have to do to keep myself alive,' Ms. Smith said.
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CBC
37 minutes ago
- CBC
The U.S. is cutting billions from science. Canadian researchers say it's time to step up
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CBC
43 minutes ago
- CBC
How an Indigenous health centre in Montreal is making care more welcoming
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Clinic staff also work to overcome deep-rooted mistrust in the health-care system. Data from a recent Statistics Canada survey found about one in five Indigenous people reported experiencing unfair treatment, racism or discrimination from a health-care professional over the previous year. Pien-Bérubé says patients at her clinic can feel safe and understood. "They are finally being heard — after how many centuries? We are finally being heard," she said. Indigenous clinic aims to close gaps outlined by TRC 7 hours ago Duration 2:14 10 years after TRC's calls to action It's been 10 years since the Truth and Reconciliation Commission, which looked to document the impact of residential schools, released its final report. In it, the commissioners pointed to "troubling gaps in health outcomes between Aboriginal and non-Aboriginal Canadians." Those include disparities in the rates of infant mortality, diabetes and suicide. Seven of the TRC's 94 calls to action focused on health, including a call to identify and close gaps in health outcomes, funding for existing and new Indigenous healing centres and recognizing the value of Indigenous healing practices. Fay Virginia Desjarlais, the family violence prevention co-ordinator at the Indigenous Health Centre of Tio'tia:ke, says the clinic is a sign there has been some progress. "There were gaps in the health system to really understand the needs of the Indigenous people living in Montreal," she said. "People didn't feel safe. A lot of advocates, elders and different organizations came together to say 'We need to do something.' " Desjarlais says hospitals and other health-care settings can be unwelcoming for many Indigenous people. She has seen patients face discrimination and racism, and has been through it herself with a family doctor. 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"I'm hopeful that once this is up and running that we have an opportunity to build centres in each of Nunavut's regions," she said. Beyond that, Aglukark wants to build up the Inuit workforce for the centre and other services and to establish more treatment centres in more communities. "It's very important for Inuit to lead and have that opportunity to provide the services in Inuktitut," she said. Dr. Terri Aldred, academic lead with the National Collaborating Centre for Indigenous Health, says progress on the calls to action around health has been "moderate." While she's impressed with new Indigenous health clinics and healing centres like the ones in Montreal and Iqaluit that are "rooted in our ways of knowing and being," Aldred says such projects need to be scaled up to meet the need. She says they also need sustainable, long-term funding. "Indigenous people that are able to access those services will start to have a different relationship with accessing health care," she said. "And we'll be able to build trust with those providers, and we'll have a positive ripple effect.

CBC
43 minutes ago
- CBC
National vaccine registry needed amid measles resurgence, Canada's outgoing top doctor says
As Dr. Theresa Tam retires as Canada's top doctor, she's calling for a national vaccine registry. Tam says the COVID-19 pandemic, which began in early 2020 and killed at least 60,000 Canadians, showed how badly one is needed to track vaccines and protect vulnerable communities. A national vaccine registry, she says, could help prevent and manage crises like the resurgence of measles that the country now faces. Tam says she's in favour of a "nationally interoperable network of vaccine registries" that connects all of the provincial and territorial health systems and helps identify pockets of the population where there is poor vaccine coverage. While the majority of measles cases so far have occurred in communities that are historically under-vaccinated, she told Dr. Brian Goldman, host of CBC's White Coat, Black Art, "we don't actually know exactly where the situation with vaccine coverage lies." Tam spoke to Goldman from Ottawa for a feature interview reflecting back on her career as the country's chief public health officer. The pandemic proved that the technology for a registry is there, she says, given that almost all provinces and territories made COVID-19 vaccine records available electronically during that time. Although it was the pandemic that made her both a household name — and a target for hate — Tam came to the role of top doctor three years earlier, in June 2017, after occupying a series of other leadership positions within the Public Health Agency of Canada (PHAC), including deputy chief. She has also served as an expert on a number of World Health Organization committees. WATCH | Dr. Theresa Tam on facing personal attacks during the pandemic: Leading Canada's public health response to COVID-19 was as much a personal challenge as it was a professional one, given Tam was also on the receiving end of racist and sexist vitriol during that time. 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Getting cross-Canada support for registry The challenge with getting a network of vaccine registries operating to help with measles and other infectious disease crises in future, Tam says, lies in getting all of the jurisdictions to sign on and co-operate to make their systems speak to one another. "There's in fact quite a lot of work on the way right now to develop those agreements with the provinces, as well as the more technical aspects of this," she said. A national registry, she says, will make things "so much easier" for public health departments, doctors, patients and parents. "That's the most important thing, that you will know whether your kids got the vaccine and that your health provider can have that information as well." Strang says there's agreement on the principle, but "the devil is always in the details." There are a number of groups, including PHAC, working to get the federation to do a better job of sharing health data, he says. "There's certainly support and agreement amongst the chief medical officers and public health leaders of this being a priority," Strang said. But Dr. Iris Gorfinkel, a Toronto family physician and researcher, says she suspects political considerations are behind some of the provinces "literally hoarding their medical data." "When politics stands in the way of science moving forward or health being prioritized, it becomes a serious, potentially life-threatening problem," said Gorfinkel, who is also the founder of PrimeHealth Clinical Research. Some provincial governments may be afraid voters will dislike sharing their health data, she says. But that shouldn't be a factor, given how easy it is to remove identifying details from the information so no one apart from an individual and their health-care provider knows their vaccine status, Gorfinkel says. We're already paying a heavy price — in lives and dollars — for not having a national registry, she says. "First, there's a tremendous waste of vaccines," Gorfinkel said. We saw that during COVID-19, she says, when Canada over-bought vaccines and struggled to administer them before they expired, eventually drawing international criticism for doing so while other parts of the world went without. In the case of the measles outbreaks, she says, "if we don't know where those are happening and we can't ship vaccines to where they're most needed, then what that means is we're not going to make the best use of the vaccines we have." And, of course, people and health systems pay when hospitals fill with people who have become ill from vaccine-preventable illnesses, Gorfinkel says. Looking abroad Other countries have made this work, among them Sweden, France, Finland, Germany, the Netherlands and Spain. In Norway, for example, a national registry that began in 1995 and at first tracked only routine childhood vaccinations, was expanded in 2011 to require mandatory reporting for all vaccines and age groups. Gorfinkel says some of these countries better embrace the sentiment that "what happens to my neighbour does affect me." Public health expert Amir Attaran, a vocal critic of Tam and PHAC during the pandemic, says far more could have been done at the federal level to get a national registry in place in this country, too. WATCH | Tam on why Canada needs better real-time health data: A professor in the faculties of law and school of epidemiology and public health at the University of Ottawa, Attaran says infectious disease experts like Tam have known since the SARS outbreak in 2003 that the country was woefully unprepared to properly track and respond to an outbreak due to poor data sharing. "And because of the experience of SARS in Canada, we should have been very switched on about this," said Attaran, who holds both a law degree and a PhD in biology. He says Canada's Statistics Act empowers the federal government to "require the provinces to cough up statistics," and that's exactly what public health data is. Canada's public health culture is self-defeating, Attaran says, because it recognizes the necessity of accurate and timely data but proceeds "under this false assumption that you can't get those data unless everybody agrees and everybody's happy with it. And then you fail to put in the political energy to bring about that consensus by agreement or coercion." Masking controversy While the pandemic highlighted the need for a national vaccine registry to manage outbreaks better, it also exposed challenges in public health communication. One of the most debated issues was masking. Attaran was among those who said Tam bungled the advice around masking in the earlier stages of the pandemic, for example. "Early in the pandemic, she told people, 'No, you don't need to mask,'" he said. Yet by then the virus had been identified as SARS-CoV-2, and we'd already learned from the 2003 SARS crisis that it required masking, he says. But in Nova Scotia, Strang says, the information scientists were working with early on suggested the virus behaved like an influenza, which spread through droplets, not aerosols. "We don't recommend widespread masking, necessarily, for everybody for influenza." Tam says public health leaders "need to do a better job in explaining to people how the scientific information are coming through, how we analyze it and how we turn them into guidance."