This study attempts to answer the question: “Is hearing the last to go?” We present evidence of hearing among unresponsive actively dying hospice patients. Individual ERP (MMN, P3a, and P3b) responses to deviations in auditory patterns are reported for conscious young, healthy control participants, as well as for hospice patients, both when the latter were conscious, and again when they became unresponsive to their environment. Whereas the MMN (and perhaps too the P3a) is considered an automatic response to auditory irregularities, the P3b is associated with conscious detection of oddball targets. All control participants, and most responsive hospice patients, evidenced a “local” effect (either a MMN, a P3a, or both) and some a “global” effect (P3b) to deviations in tone, or deviations in auditory pattern. Importantly, most unresponsive patients showed evidence of MMN responses to tone changes, and some showed a P3a or P3b response to either tone or pattern changes. Thus, their auditory systems were responding similarly to those of young, healthy controls just hours from end of life. Hearing may indeed be one of the last senses to lose function as humans die.

Plague is an age-old disease that can still be deadly today, but now researchers are developing new vaccines that could potentially protect against plague infection, early research in animals suggests.

In a new study, researchers tested three vaccines that were designed to protect people against infection from the bacteria that cause plague, known as Yersinia pestis. To create the vaccines, the researchers modified several genes of the bacteria so that they couldn’t cause disease, but would likely trigger an immune response in an animal. Specifically, the vaccines were designed to protect people against the bacteria that cause pneumonic plague, the most serious form of plague and the only type that spreads through airborne transmission.

Synairgen, a drug company founded by professors from the University of Southampton, UK, has announced promising results from its clinical trial of SNG001 – an inhaled formulation of interferon beta, in hospitalised COVID-19 patients.

17 years after the Human Genome Project, researchers unlocked the X chromosome.

Circa 2016

In a world first, Australian scientists have figured out how to reprogram adult bone or fat cells to form stem cells that could potentially regenerate any damaged tissue in the body.

The researchers were inspired by the way salamanders are able to replace lost limbs, and developed a technique that gives adult cells the ability to lose their adult characteristics, multiply and regenerate multiple cell types — what is known as multipotency. That means the new stem cells can hypothetically repair any injury in the body, from severed spinal cords to joint and muscle degeneration. And it’s a pretty big deal, because there are currently no adult stem cells that naturally regenerate multiple tissue types.

“This technique is a significant advance on many of the current unproven stem cell therapies, which have shown little or no objective evidence they contribute directly to new tissue formation,” said lead researcher John Pimanda from the University of New South Wales, Faculty of Medicine (UNSW Medicine). “We are currently assessing whether adult human fat cells reprogrammed into [induced multipotent stem cells (iMS cells)] can safely repair damaged tissue in mice, with human trials expected to begin in late 2017.”