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A decade in the making, NASA and SpaceX have set May 27 as the target launch date for the first crewed space mission to launch into orbit from U.S. soil since the retirement of the space shuttle in 2011.

NASA astronauts Doug Hurley and Bob Behnken, two veterans of the shuttle program, will ride SpaceX’s Crew Dragon spacecraft into orbit on top of a Falcon 9 rocket from pad 39A at NASA’s Kennedy Space Center in Florida. That’s the same historic launch facility used by the last space shuttle flight.

Liftoff time on May 27 is expected to be around 4:32 p.m. EDT (2032 GMT), when the Earth’s rotation brings the launch pad under the orbital plane of the International Space Station.

Talk being ahead of the curve;


Event 201 was a 3.5-hour pandemic tabletop exercise that simulated a series of dramatic, scenario-based facilitated discussions, confronting difficult, true-to-life dilemmas associated with response to a hypothetical, but scientifically plausible, pandemic. 15 global business, government, and public health leaders were players in the simulation exercise that highlighted unresolved real-world policy and economic issues that could be solved with sufficient political will, financial investment, and attention now and in the future.

The exercise consisted of pre-recorded news broadcasts, live “staff” briefings, and moderated discussions on specific topics. These issues were carefully designed in a compelling narrative that educated the participants and the audience.

The Johns Hopkins Center for Health Security, World Economic Forum, and Bill & Melinda Gates Foundation jointly propose these recommendations.

The discovery that immune T cells have a spectrum of responsiveness could shed light on how our immune system responds to infections and cancer, and what goes wrong in immune diseases. Researchers at the Wellcome Sanger Institute, Open Targets, Biogen, GSK and their collaborators found that T cells responded very differently to immune signals the more ‘training’ they had been exposed to, rather than being a simple switch from naïve to experienced. This could help guide research into finding drug targets for immune diseases such as asthma and rheumatoid arthritis.

Today’s study (14th April), published in Nature Communications, also revealed that even highly trained memory T cells are less rigidly specialized than previously thought, and are able to respond to new immune signals. This has implications for immune research, and could help understand for example how the body responds to infections.

T cells are key white blood cells that fight infection and disease, and act like police directing the immune system response. Babies are born with inexperienced — naïve — T cells, which change as they come into contact with bacteria or viruses, to create specific memory T cells that can ‘remember’ fighting against these infections. These memory T cells can then react more quickly the next time they meet the same threat, telling the immune system to remove the infection rapidly. This is how vaccination protects against disease, by delivering a safe form of an invading virus or bacterium, to train our immune system by building up specific memory T cells.