It originated in middle school.
Anika Chebrolu, 14, of Frisco, Texas, has won this year’s 3M Young Scientist Challenge for her work finding a molecule that can selectively bind to the virus’s spike protein, according to the contest organizers. The eight grader used in-silico methodology for drug discovery to do it.
This includes volunteering to test the new vaccine being developed by the Israeli Institute for Biological Research in Ness Ziona. Meet some of the heroes who are doing their bit for humanity.
The research center said it will begin the clinical trials phase of its COVID-19 vaccine in November and about one hundred Israelis aged 18–55 are expected to participate by the time the trials are over. The first phase will include three brave volunteers and will take place in Sheba Medical Center in Tel HaShomer and Hadassah Medical Center in Jerusalem.
As with any other clinical trials, participants will be divided into two groups: those who will receive the real vaccine and those who will receive a fake vaccine, also known as placebo.
In a major breakthrough an international team of scientists, led by the University of Bristol, has potentially identified what makes SARS-CoV-2 highly infectious and able to spread rapidly in human cells. The findings, published in Science today [20 October] describe how the virus’s ability to infect human cells can be reduced by inhibitors that block a newly discovered interaction between virus and host, demonstrating a potential anti-viral treatment.
Have you gotten your genome sequenced yet? How important do you think genetic testing is to planning your own personalized longevity regimen?
We cover the benefits of genetic testing for longevity, and why you should consider getting a DNA test if you want to extend your lifespan.
Someone from Oxford’s vaccine trial has passed away.
BRAZIL’S health authority has confirmed a volunteer has died after participating in the clinical trials of the coronavirus vaccine developed by AstraZeneca and Oxford University.
Self healing material is being developed for prosthetic limbs.
This material can help us make self-healing prosthetic limbs in the future.
Using the Crispr gene-editing technique that won a recent Nobel Prize, Crispr Therapeutics cleared blood cancers in patients with off-the-shelf immune cells. These so-called CAR-T therapies previously required a patient’s own cells.
In a Wednesday morning announcement, Crispr Therapeutics (ticker: CRSP) said that its gene-editing let doctors use cells from healthy donors—opening up prospects for broadly available, less-expensive use of CAR-T treatment.
In the Phase 1 trial, the lymphoma blood cancer in four of 11 patients responded completely to infusions of T cells whose genes were altered to target the cancer and prevent transplant rejection. Standard treatments had failed all participants. In patients that got higher doses, the complete responses have lasted for months.
Our immune system’s capacity to mount a well-regulated defense against foreign substances, including toxins, weakens with age and makes vaccines less effective in people over age 65. At the same time, research has shown that immunotherapy targeting neurotoxic forms of the peptide amyloid beta (oligomeric Aβ) may halt the progression of Alzheimer’s disease, the most common age-related neurodegenerative disease.
A team led by Chuanhai Cao, Ph.D., of the University of South Florida Health (USF Health), has focused on overcoming, in those with impaired immunity, excess inflammation and other complications that interfere with development of a therapeutic Alzheimer’s vaccine.
Now, a preclinical study by Dr. Cao and colleagues indicates that an antigen-presenting dendritic vaccine with a specific antibody response to oligomeric Aβ may be safer and offer clinical benefit in treating Alzheimer’s disease. The vaccine, called E22W42 DC, uses immune cells known as dendritic cells (DC) loaded with a modified Aβ peptide as the antigen.
WASHINGTON (AP) — Drugmaker Purdue Pharma, the company behind the powerful prescription painkiller OxyContin that experts say helped touch off an opioid epidemic, will plead guilty to federal criminal charges as part of a settlement of more than $8 billion, the Justice Department announced Wednesday.
The deal does not release any of the company’s executives or owners — members of the wealthy Sackler family — from criminal liability, and a criminal investigation is ongoing. Family members said they acted “ethically and lawfully,” but some state attorneys general said the agreement fails to hold the Sacklers accountable.
The company will plead guilty to three counts, including conspiracy to defraud the United States and violating federal anti-kickback laws, the officials said, and the agreement will be detailed in a bankruptcy court filing in federal court.
