Historic $64 million NIH Award for Palliative Care Research ushers in new era; Icahn School of Medicine at Mount Sinai to lead
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Updates every hour. Last Updated: 13-Jan-2026 04:11 ET (13-Jan-2026 09:11 GMT/UTC)
An innovative method that uses modified versions of a bacterial virus effective at delivering treatments to human cells shows promise as a more inexpensive and efficient way to treat some deadly genetic diseases.
Researchers from the School of Pharmacy at the University of Waterloo use a modified version of a bacterial virus called M13 to target specific human cells while carrying only the genes they want delivered, with no unwanted virus or bacteria. Scientists can fine-tune the modified M13 to deliver different therapeutic genes for the treatment of many different diseases.
When SARS-CoV-2, the coronavirus that causes COVID-19, began spreading worldwide in 2020, many research teams immediately set to work developing a vaccine against it. Building on decades of previous work on mRNA technology and on other viral vaccines, including HIV, they achieved their goal within the year. The most widely used mRNA vaccine design contains the genetic instructions for the body to make the spike protein that the virus uses to enter cells. The resulting immune response protects against infection and, more importantly, disease and death. However, developing a vaccine for HIV has proven much more difficult.
Overly aggressive treatment of diabetes and hypertension in older adults is causing preventable harm—including dangerously low blood sugar or blood pressure, hospitalizations, disability and even death. Despite existing guidelines urging individualized, cautious care, these complications remain widespread, especially among frail seniors and nursing home residents. Researchers call for urgent change in how health care providers are supported and held accountable. They argue that they should be actively encouraged – not merely expected – to avoid overtreatment through carefully designed quality measures.