Recent findings at the University of Finland and UVA School of Medicine have overturned 300 years of accepted anatomical fact. Until recent years, the scientific community believed that the lymphatic system — which functions in the body to remove waste and toxins — did not extend into the human brain.
Then came Kari Alitalo. Kari desired a better map of the lymphatic vessels, so three years ago he dosed the lymph cells of mice with a glowing jellyfish gene. At the end of the experiment, he was shocked to see that the mice’s heads were glowing. To be certain his results were correct, he repeated the experiment. His repeat showed exactly the same phenomenon.
As it turns out, Kari had discovered what he termed to be the glymphatic system — the division of the lymphatic system that exists as “glia” cells in the brain.
The Glymphatic System
As it turns out, the glymphatic system may have major implications for degenerative diseases. It’s possible that Alzheimer’s, Huntington’s, and Parkinson’s diseases could be effected by dysfunction in the glymphatic system. A dysfunctional lymphatic system can lead to a buildup of toxins and waste in the body — and a dysfunctional glymphatic system may lead to a buildup of toxins in the brain.
Early studies at Yale and Oregon Health & Science University suggest that a functioning glymphatic system is essential to a healthy brain. Harvard has shown that glymphatic flow is decreased right before a migraine. Research has also shown that the glymphatic system works best when we are asleep, and that sleeping on your side is better than sleeping on your stomach or back.
It’s clear that this revolutionary anatomical discovery will have major impact for clinical therapies for all kinds of neurodegenerative diseases. Read the full article from the Washington Post here, and make sure to subscribe to our blog for the latest news and events across the biotech world.
Alzheimer’s PET Scan – US National Institute on Aging, Alzheimer’s Disease Education and Referral Center
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Although metastasis is the leading cause of death among people with cancer, for the most part, researchers are stumped about which molecular signals allow malignant cells to leave primary tumors and start new ones. Two studies published in Nature this month highlight roles in metastasis for an unexpected group of molecules—lipids.
A preventive DNA vaccine encoding two Zika structural proteins protected Rhesus macaques from viral infection. The results, published today (September 22) in Science, are encouraging for organizers of the ongoing Phase 1 clinical trial testing one of the two vaccines examined in this nonhuman primate study. The new work suggests a minimal antibody level in the blood that is likely necessary for protection against Zika virus infection in in people.
Researchers design a Cas9 enzyme that cuts DNA only in the presence of particular drug.
There are various ways to turn CRISPR/Cas9’s gene-editing activity on and off in cells, such as exposing tailor-made Cas9 enzymes to a particular type of light or to specific drugs. Each technique developed so far has drawbacks—either being complicated or irreversible. So researchers took inspiration from the Cre-recombinase-based method to control gene expression and built a “user-friendly” protocol for reversibly activating and inactivating CRISPR.
The benefits of the cholesterol-reducing drug statins are underestimated and the harms exaggerated, a major review suggests.
Published in the Lancet and backed by a number of major health organisations, it says statins lower heart attack and stroke risk.
The review also suggests side effects such as muscle pain do occur, although in relatively few people.
But critics say healthy people are unnecessarily taking medication.
Statins reduce the build-up of fatty plaques that lead to blockages in blood vessels. According to the report authors:
About six million people are currently taking statins in the UK
Of those, two million are on them because they have already had a heart attack, stroke or other cardiovascular event
The remaining four million take statins because of risk factors such as age, blood pressure or diabetes
Up to two million more should possibly take statins
The Lancet review, led by Prof Rory Collins from the Clinical Trial Service Unit at the University of Oxford, looked at the available evidence for the effects of taking an average 40mg daily dose of statins in 10,000 patients over five years.
It suggested cholesterol levels would be lowered enough to prevent 1,000 “major cardiovascular events” such as heart attacks, strokes and coronary artery bypasses in people who had existing vascular disease – and 500 in people who were at risk due to age or other illnesses such as high blood pressure or diabetes.
IMM-101 drug has extended lives of people with metastatic pancreatic cancer and appears to have no side-effects
A new drug that “wakes up” the immune system to attack cancer has extended the lives of people with metastatic pancreatic cancer and has no side-effects, raising hopes for a new and powerful tool against the most intractable form of the disease.
The drug, IMM-101, is considered groundbreaking because pancreatic cancer that has spread to other parts of the body usually kills within a few months.
The patients who were given the new immunotherapy drug actually felt better than those who were on standard chemotherapy, said Angus Dalgleish, professor of oncology at St George’s, University of London, who led the research.
Dalgleish is excited by the potential of the immunotherapy drug, although the trial is relatively small, involving 110 people. Only 18% of patients with advanced pancreatic cancer are alive after one year and 4% after five years, so new treatments for the disease are badly needed.
Study found a gap between resources, potential need in the case of a U.S. outbreak
As summer drew near, the nation’s health officials took stock of whether they could handle a surge in demand for Zika diagnostic tests if disease-carrying mosquitoes began to proliferate.
A survey of state and local laboratories found enough capacity to perform 3,500 to 5,000 tests a week for the Zika virus. But that wouldn’t be enough to meet demand under the Centers for Disease Control and Prevention’s worst-case scenario for a domestic Zika outbreak.
The gap was “considerable,” said Kelly Wroblewski, director of infectious diseases for the Association of Public Health Laboratories, which conducted the April survey.
The finding set off a rush to expand lab capacity that continues as Zika’s foothold in the U.S. expands. In recent months, dozens of public health laboratories—which work with the government to monitor public health and screen for disease—bought equipment, stockpiled supplies and trained employees needed to start Zika testing, said state and local health officials.
Twelve California public health labs are preparing to start performing Zika tests; five others already do. The health department in Houston conducts one type of Zika test and will perform a second “as soon as we can get the equipment in the door,” said Larry Seigler, director of the city’s health labs.
The recent regulatory approval of the first hematopoietic stem and progenitor cell gene therapy (HSPC-GT) signals the start of a new era for gene therapy and highlights the potential contribution by high-throughput cell culture technologies in propelling HSPC-GT from curing rare diseases to curing more common diseases.
Hematopoietic stem cells (HSCs) are the “fountain” for all blood cells that circulate in our bodies throughout life. Arguably, no other cell type has more profound and far-reaching influence on our well-being than HSCs. They reside in our bone marrow and continuously produce a variety of cells with vital tasks, for example, oxygenation via red blood cells, termination of bleeding via platelets, and immunity via leukocytes, which also provide immune defense to the central nervous system.
There is, however, a flipside to the pre-eminence of HSCs. When faulty HSCs emerge, devastating outcomes can ensue, such as autoimmune diseases like multiple sclerosis and blood cancers like leukemia. Thankfully, a solution to these life-threatening indications is well at hand because HSCs can be removed and replaced with healthy HSCs using HSC transplantation (HSCT)—a highly effective procedure pioneered by Nobelist E. Donnall Thomas over five decades ago.