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Alzheimer's Research

Micro-Particles Carrying Multiple Vaccine Doses Could Reduce Need for Follow-Up Shots

New polymer microparticles can be used to deliver vaccines at different times. The work could lead to childhood vaccines given just once, eliminating the need for booster doses.

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The development of micro-particles that can carry and release multiple vaccine doses has the potential to revolutionize the way vaccines are administered. Researchers at MIT have been working on this technology, which could make it possible for children to receive all their vaccines in just one shot. This is especially important in areas where access to healthcare facilities is limited.

The researchers used a type of polymer called polyanhydride, which is biodegradable and creates a less acidic environment as it breaks down. They were able to use this material to create micro-particles that could deliver two doses of diphtheria vaccine – one released immediately, and the second two weeks later. The results showed that mice receiving this vaccine generated as many antibodies as those receiving two separate doses two weeks apart.

The researchers hope to extend the intervals between doses, making these particles useful for delivering childhood vaccines that require multiple doses over several months. They also developed a machine-learning model to predict how long it takes for the particles to degrade once in the body, which could be used to develop materials that release their payload after longer intervals – months or even years.

This technology has broad potential and could be adapted to deliver other types of vaccines, as well as small molecules or biologics that require durability or multiple doses. The researchers are hopeful that this will make it easier for children living in areas where healthcare facilities are limited to receive the vaccines they need.
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The study was funded by the Koch Institute Support (core) Grant from the National Cancer Institute, and its findings were published in the journal Advanced Materials.

Alzheimer's

“Unlocking Brain Health: Scientists Discover Key Receptor for Microglia to Fight Alzheimer’s”

Scientists at UCSF have uncovered how certain immune cells in the brain, called microglia, can effectively digest toxic amyloid beta plaques that cause Alzheimer’s. They identified a key receptor, ADGRG1, that enables this protective action. When microglia lack this receptor, plaque builds up quickly, causing memory loss and brain damage. But when the receptor is present, it seems to help keep Alzheimer’s symptoms mild. Since ADGRG1 belongs to a drug-friendly family of receptors, this opens the door to future therapies that could enhance brain immunity and protect against Alzheimer’s in more people.

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The scientific community has made significant strides in understanding the complex mechanisms behind Alzheimer’s disease. A recent study by researchers at UC San Francisco has shed light on how microglia, immune cells that play a crucial role in maintaining brain health, can break down and remove toxic proteins associated with the disease. This groundbreaking discovery could pave the way for novel therapeutic approaches to combat Alzheimer’s.

In Alzheimer’s, proteins like amyloid beta clump together, forming plaques that damage the brain. However, in some individuals, microglia effectively engulf and digest these proteins before they can cause harm. The resulting few and smaller clumps are associated with milder symptoms. Researchers at UCSF identified a molecular receptor, ADGRG1, which enables microglia to perform this critical function.

Using a mouse model of Alzheimer’s disease, the researchers observed that the loss of ADGRG1 led to a rapid buildup of amyloid plaques, neurodegeneration, and problems with learning and memory. The study also reanalyzed data from a prior human brain expression study, finding that individuals who died of mild Alzheimer’s had microglia with abundant ADGRG1, whereas those with severe Alzheimer’s had very little ADGRG1.

This discovery has significant implications for the development of new therapies. Since ADGRG1 is one of hundreds of G protein-coupled receptors targeted in drug development, it may be feasible to rapidly translate this finding into new treatments. As Dr. Piao noted, “Some people are lucky to have responsible microglia, but this discovery creates an opportunity to develop drugs to make microglia effective against amyloid-beta in everyone.” The potential for breakthrough therapies is exciting news for those affected by Alzheimer’s and their loved ones.

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Alzheimer's Research

Walking 7000 Steps a Day Can Be Just as Beneficial as 10,000 – Here’s Why

Walking 7000 steps a day may be just as powerful as hitting the much-hyped 10,000-step goal when it comes to reducing the risk of early death and disease. A sweeping global review of 57 studies shows that 7000 steps per day slashes the risk of dying early by nearly half—and brings major benefits across heart health, dementia, depression, and more. The bonus? Even walking from 2000 to 4000 steps per day brings measurable improvements. For millions of people, this study redefines what it means to “move enough.”

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The study, led by Professor Melody Ding from the University of Sydney, has made a groundbreaking discovery that walking 7000 steps a day can offer similar health benefits as walking 10,000 steps. This finding is based on an analysis of data from 57 studies conducted in over ten countries between 2014 and 2025.

The researchers examined the impact of different daily step counts on various health outcomes, including cardiovascular disease and cancer. They found that walking at least 7000 steps a day can significantly improve eight major health outcomes, such as reducing the risk of cardiovascular disease, dementia, and depressive symptoms.

Professor Melody Ding emphasized that aiming for 7000 steps is a realistic goal for people who struggle to meet traditional exercise guidelines. “Even small increases in step counts, like going from 2000 to 4000 steps a day, are associated with significant health gains,” she said.

The researchers compared the health outcomes of people walking at different step increments, starting at 2000 steps per day. They found that:

* When compared to 2000 steps a day, walking 7000 steps a day was associated with a 47% lower risk of death from cardiovascular disease and cancer.
* For those who cannot yet achieve 7000 steps a day, even small increases in step counts can lead to significant health improvements.

Experts are calling for future studies to explore how step goals should vary based on age, health status, and region. They also suggest including diverse populations and longer-term data to strengthen the evidence. Professor Ding emphasizes that this kind of detail is rare and will be useful for health practitioners when tailoring advice for patients.

Overall, the study suggests that walking 7000 steps a day can be a more achievable and beneficial goal than previously thought, and even small increases in daily movement can lead to meaningful health improvements.

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Alzheimer's

Rewinding Stroke Damage and Beyond: The Promise of GAI-17

Stroke kills millions, but Osaka researchers have unveiled GAI-17, a drug that halts toxic GAPDH clumping, slashes brain damage and paralysis in mice—even when given six hours post-stroke—and shows no major side effects, hinting at a single therapy that could also tackle Alzheimer’s and other tough neurological disorders.

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The devastating effects of stroke can be irreversible, leading to loss of neurons and even death. However, researchers have made a groundbreaking discovery that may change this grim reality. A team led by Osaka Metropolitan University Associate Professor Hidemitsu Nakajima has developed a revolutionary drug called GAI-17, which inhibits the protein GAPDH involved in cell death.

GAPDH, or glyceraldehyde-3-phosphate dehydrogenase, is a multifunctional protein linked to various debilitating brain and nervous system diseases. The team’s innovative approach was to create an inhibitor that targets this protein, preventing its toxic effects on neurons. When administered to model mice with acute strokes, GAI-17 showed astonishing results: significantly reduced brain cell death and paralysis compared to untreated animals.

The significance of GAI-17 extends far beyond stroke treatment. Experiments revealed no adverse effects on the heart or cerebrovascular system, making it a promising candidate for addressing other intractable neurological diseases, including Alzheimer’s disease. Moreover, the drug demonstrated remarkable efficacy even when administered six hours after a stroke – a critical window that could revolutionize stroke care.

“We believe our GAPDH aggregation inhibitor has the potential to be a single treatment for many debilitating neurological conditions,” Professor Nakajima expressed. “We will continue to explore its effectiveness in various disease models and strive towards creating a healthier, longer-lived society.”

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