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A new coating method in mRNA engineering points the way to advanced therapies

Researchers from Tokyo Medical and Dental University (TMDU) have developed a novel method for chemically modifying engineered messenger RNA molecules,…

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Researchers from Tokyo Medical and Dental University (TMDU) have developed a novel method for chemically modifying engineered messenger RNA molecules, allowing greater control of their biological functions and advancing mRNA therapeutic technologies

Credit: Department of Advanced Nanomedical Engineering, TMDU

Researchers from Tokyo Medical and Dental University (TMDU) have developed a novel method for chemically modifying engineered messenger RNA molecules, allowing greater control of their biological functions and advancing mRNA therapeutic technologies

Tokyo, Japan – Medicine can help to treat certain illnesses, e.g., antibiotics can help overcome infections, but a new, promising field of medicine involves providing our body with the “blueprint” for how to defeat illnesses on its own.

mRNA therapeutics is the delivery of messenger RNA (mRNA) molecules into the body, which the cellular machinery can use to make specific proteins. The field is rapidly advancing, especially because mRNA vaccines proved successful against COVID-19. However, the delivery of these engineered mRNAs to a specific organ has proved challenging.

Now, a team at Tokyo Medical and Dental University (TMDU) has shown that coating the engineered mRNAs with a molecule called polyethylene glycol, or PEG, allows their delivery selectively to the spleen.

To understand this achievement, let’s first discuss how mRNA therapeutics has worked until now. Engineered mRNAs have been packaged into structures called “polyplexes” for delivery into the body. The polyplex structures allow mRNAs to remain stable while outside cells and to be released in a controlled manner once inside cells. Once inside, the mRNAs are used by cellular machinery to produce proteins that are naturally dysfunctional or absent.

Without modification, the polyplexes tend to accumulate in the lungs, as after injection into the blood they rapidly stick to each other and surrounding proteins and cells and become lodged in the lung’s blood vessels. Treating polyplexes with PEG, a process called “PEGylation”, prevents them from sticking together; however, applying PEG in a controlled, consistent manner to the polyplex surface is very difficult.

The team at TMDU has developed a new method of PEGylation, where the mRNAs are hybridized to PEG molecules before the polyplexes are formed. Using this method, almost all the PEG strands mixed into the reaction become bound to the polyplexes, allowing much greater control over the final amount of PEG on the polyplex surface.

Using a mouse model, the team found that the quantities and lengths of the PEG molecules significantly affected how well the mRNA therapy worked. A small number of short PEG molecules prevented accumulation of the engineered mRNAs in the lungs, facilitating effective delivery to the spleen. This approach has demonstrated utility in mRNA vaccines.

“Our novel method allows fine tuning of the amount of PEGylation of mRNA polyplexes,” explains senior author Dr. Satoshi Uchida, “which in turn allows control of the physicochemical properties of the polyplexes, and thus their biological functionalities.”

mRNA technology has wide-ranging potential for treating many diseases that have previously been considered incurable, as well as for the development of novel cancer treatments and vaccines. The development of this innovative technique paves the way for significant advances in the therapeutic use of mRNA polyplexes, with far-reaching potential consequences for human health.

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The article, “Poly(ethylene Glycol) (PEG)–OligoRNA Hybridization to mRNA Enables Fine-Tuned Polyplex PEGylation for Spleen-Targeted mRNA Delivery”, was published in Small Science at DOI: 10.1002/smsc.202300258.


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International

CAMH develops first ever clinically validated natural supplement to prevent postpartum blues

A new study published in the Lancet discovery science  journal eClinicalMedicine has confirmed that a novel natural supplement—invented, researched,…

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A new study published in the Lancet discovery science  journal eClinicalMedicine has confirmed that a novel natural supplement—invented, researched, developed and commercialized at the Centre for Addiction and Mental Health (CAMH)—prevents postpartum blues, and reduces symptoms of postpartum depression over the following six months after giving birth.

Credit: Image courtesy of CAMH. All rights reserved.

A new study published in the Lancet discovery science  journal eClinicalMedicine has confirmed that a novel natural supplement—invented, researched, developed and commercialized at the Centre for Addiction and Mental Health (CAMH)—prevents postpartum blues, and reduces symptoms of postpartum depression over the following six months after giving birth.

Up to 8 out of ten new mothers experience postpartum, or ‘baby,’ blues, characterized by mood swings, crying spells, anxiety and difficulty sleeping. The condition usually begins within the first few days after delivery and may last for up to two weeks. Postpartum blues strongly raises the risk of postpartum depression, a serious mental illness affecting 13 per cent of mothers. Postpartum depression has important health care consequences: impairing quality of life, increasing risk for future depressive episodes and suicide, and is associated with cognitive and emotional effects in children. Until now, options for widespread prevention have been lacking for either condition.

The study, entitled Dietary Supplement for Mood Symptoms in Early Postpartum: A Double-Blind Randomized Placebo Controlled Trial, involved more than 100 postpartum participants between January 2019 and December 2022 who either took four doses of the natural supplement several days after giving birth, or a matching placebo. Within the supplement group, two-thirds (66 per cent) experienced either no symptoms or only negligible symptoms of postpartum blues. Furthermore, in the following six months, participants who received the supplement experienced less symptoms of depression with none reaching the clinical threshold of postpartum depression six months after giving birth.

“Globally 140 million births take place every year. Most women then experience postpartum blues, which, when severe, increases the likelihood of getting full-blown postpartum depression at least fourfold. Our study showed that both postpartum blues and later symptoms of depression were lower in women who received the dietary supplement,” said Dr. Jeffrey Meyer, inventor of the nutraceutical and study senior author. “Providing this specialized dietary support in the first few days after giving birth is a crucial window to avoid depressive symptoms which is tremendously important given there is considerable risk that they may recur and have lifelong impact.”

Dr. Meyer has been investigating postpartum blues for more than 15 years. His previous imaging research found that a protein called MAO-A rises dramatically in the brains of postpartum women and this protein removes important brain chemicals—like serotonin and dopamine—that support normal mood. It also acts as an oxidant and is linked to the development and progression of certain mental illnesses. To combat this effect, the nutraceutical is made up of a patented unique combination of natural ingredients, including blueberry extract, which contain antioxidants, and amino acids that replenish essential neurochemicals in the brain to support healthy mood and the ability to concentrate under stress. The supplement was well tolerated and women who took it tended to report less symptoms, in part due to less drowsiness, headache and restlessness. The researchers previously showed that the amino acids in the supplement do not affect their total concentrations in breast milk, which was expected since these amino acids are already found in proteins in breast milk.     

CAMH has partnered with international women’s health supplement and pharmaceutical company Exeltis via a licensing agreement to bring the product to market under the name Blues Away®. Exeltis has maintained the natural health product approach in their preparations and manufacture for widespread distribution of the supplement. It is expected that the product will be available for sale in the U.S. beginning April 11, 2024.  It is also in the process of being brought to other global markets—including Canada—with the pace of approvals being dependent on each country’s regulatory requirements and reviews. 

“We are thrilled to unveil the culmination of years of dedication and collaboration in the form of our groundbreaking nutraceutical for postpartum blues prevention. It is great that we are able to simultaneously share our clinical research around this product while also partnering with a  global women’s health industry leader to make it available to the new mothers who need it,” said Klara Vichnevetski, Director of Industry Partnerships and Technology Transfer. CAMH has nurtured this innovation from its inception, guiding it from bench to bedside where it can make an immediate and profound difference in the lives of millions of women and their families.”

A limitation of the study was that, of the several measures of depression in the study, the supplement did not demonstrate the expected protective effect in an experimental test that involves inducing low mood with sad stimuli, although it is possible that the stress of the COVID-19 pandemic and moving the setting of the study to participant’s homes during the pandemic may have influenced the results of this particular test.

Aristotle Voineskos, Vice President of Research, added: “Two major pillars of our CAMH approach to research are the importance of integrating scientific findings into advancing mental health care and the value of early intervention. Through the perseverance and dedication of our researchers and technology transfer team, this novel preventative therapy may contribute to best practice when it comes to postpartum care and help women around the world avoid more serious and chronic mental illness.”

This research was funded by CAMH, with some additional funding from Exeltis.

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About the Centre for Addiction and Mental Health (CAMH)

CAMH is Canada’s largest mental health and addiction teaching hospital and a world leading research centre in this field. CAMH combines clinical care, research, education, policy development and health promotion to help transform the lives of people affected by mental illness and addiction. CAMH is fully affiliated with the University of Toronto, and is a Pan American Health Organization/World Health Organization Collaborating Centre. For more information, please visit camh.ca or follow @CAMHnews on Twitter.

Media Contact:

CAMH Media Relations
media@camh.ca


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Spread & Containment

‘Bird Flu-Pocalypse’ Forces Hong Kong To Suspend Some Imports Of US Poultry Meat

‘Bird Flu-Pocalypse’ Forces Hong Kong To Suspend Some Imports Of US Poultry Meat

The recent spread of bird flu—also known as highly pathogenic…

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'Bird Flu-Pocalypse' Forces Hong Kong To Suspend Some Imports Of US Poultry Meat

The recent spread of bird flu—also known as highly pathogenic avian influenza, or HPAI— across several US states has been hyped by corporate media. Some journalists are quoting 'experts' who warn the bird flu pandemic could be '100 times worse' than Covid.' 

According to Bloomberg data, the story count in corporate media for all things "Bird Flu" last week hit a record high on data going back to 2014. 

The context here is crucial. Bird flu is not just a US issue anymore; it's 'going global,' and this is happening just before the US presidential elections in November.  

On Tuesday, Hong Kong's food safety authority published a memo stating, "Import of poultry meat and poultry products suspended in some areas of the United States." 

Here's the full memo from the Center for Food Safety (CFS) of the Food and Environmental Hygiene Department:

The Center for Food Safety (CFS) of the Food and Environmental Hygiene Department announced today (April 9) that in response to a notification from the World Organization for Animal Health regarding an outbreak of highly pathogenic H5N1 avian influenza in Ionia County, Michigan, and Parmer County, Texas, USA, The CFS immediately instructed the trade to suspend the import of poultry meat and poultry products (including poultry eggs) from the above-mentioned areas to protect public health in Hong Kong.

A spokesman for the CFS said that according to the Census and Statistics Department, Hong Kong imported about 37,770 tonnes of chilled and frozen poultry meat and about 83.84 million poultry eggs from the United States last year.

The spokesman said: "The CFS has contacted the US authorities regarding the incident and will continue to closely monitor information on the outbreak of avian influenza from the World Organization for Animal Health and relevant authorities, and will take appropriate actions in light of the development of the local epidemic."

If it's bird flu or whatever "Disease X" could possibly be, there appears to be a push to "intersect" some type of 'Covid crisis' before the 2024 US elections.

"They will surely try to run their "Disease X" ruse. But they have already lost the trust of the people they made war against in their own country. In which case, expect resistance among the un-sick," James Howard Kunstler penned in a note earlier this month.

Tyler Durden Tue, 04/09/2024 - 21:20

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Government

15 US Agencies Knew Wuhan Lab Was “Trying To Create A Coronavirus Like COVID-19”: Rand Paul

15 US Agencies Knew Wuhan Lab Was "Trying To Create A Coronavirus Like COVID-19": Rand Paul

While a massive body of evidence exists on the…

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15 US Agencies Knew Wuhan Lab Was "Trying To Create A Coronavirus Like COVID-19": Rand Paul

While a massive body of evidence exists on the origins of COVID-19, Senator Rand Paul (R-KY) is conducting his own investigation into the matter.

In a Tuesday op-ed, Paul writes that government officials from 15 federal agencies "knew in 2018 that the Wuhan Institute of Virology was trying to create a coronavirus like COVID-19."

These officials knew that the Chinese lab was proposing to create a COVID 19-like virus and not one of these officials revealed this scheme to the public. In fact, 15 agencies with knowledge of this project have continuously refused to release any information concerning this alarming and dangerous research.

Government officials representing at least 15 federal agencies were briefed on a project proposed by Peter Daszak’s EcoHealth Alliance and the Wuhan Institute of Virology. -Rand Paul

Paul is talking about the DEFUSE project, which was revealed after DRASTIC Research uncovered documents showing that DARPA had been presented with a proposal for EcoHealth to perform gain-of-function research on bat coronavirus.

And according to Rand Paul, officials from 15 agencies knew about this. While the project was never funded (DARPA called it too dangerous) - Paul writes: "This project, the DEFUSE project, proposed to insert a furin cleavage site into a coronavirus to create a novel chimeric virus that would have been shockingly similar to the COVID-19 virus."

And what does this mean?

It means that at least 15 federal agencies knew from the beginning of the pandemic that EcoHealth Alliance and the Wuhan Institute of Virology were seeking federal funding in 2018 to create a virus genetically very similar if not identical to COVID-19.

Disturbingly, not one of these 15 agencies spoke up to warn us that the Wuhan Institute of Virology had been pitching this research. Not one of these agencies warned anyone that this Chinese lab had already put together plans to create such a virus.

Peter Daszak concealed this proposal. University of North Carolina scientist Ralph Baric, a named collaborator on the DEFUSE project, failed to reveal that the Wuhan Institute of Virology had already proposed to create a virus similar to COVID-19.

And now we know that 15 agencies heard the proposal and when each agency discovered that COVID-19 was strangely similar to DEFUSE’s proposed virus creation, not one agency head stepped forward to warn the public that the virus might be man-made and therefore already adapted to transmit freely among humans. -Rand Paul

Paul further writes that Fauci's NIAID was not only briefed on the DEFUSE proposal, his "Rocky Mountain Lab" was named as a partner in it along with the Wuhan Institute of Virology.

Meanwhile, researcher Ian Lipkin, one of the authors of the "proximal origins" coverup paper, was also part of the DEFUSE plan - which he never revealed publicly.

"Did NIAID warn us? Did Anthony Fauci warn us? No! All lips remained sealed," writes Paul.

Tyler Durden Tue, 04/09/2024 - 20:00

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