Faith Jones – Lifeboat News: The Blog https://lifeboat.com/blog Safeguarding Humanity Mon, 04 Apr 2022 21:02:36 +0000 en-US hourly 1 https://wordpress.org/?v=6.7.1 Scientist Who Genetically Modified Human Babies Released From Prison https://lifeboat.com/blog/2022/04/scientist-who-genetically-modified-human-babies-released-from-prison Mon, 04 Apr 2022 21:02:36 +0000 https://lifeboat.com/blog/2022/04/scientist-who-genetically-modified-human-babies-released-from-prison

Remember He Jiankui, the Chinese scientist who shocked the world when it emerged in late 2018 that he had used CRISPR to tinker with the genetic code of IVF embryos, leading to the birth of twins who are likely the world’s first genetically modified humans?

The news led to a broad outcry among scientists, ethicists and regulators, not the least because experts in the field later found the experiment to be tainted by “egregious scientific and ethical lapses.”

Long story shot, China ended up imprisoning He, who also lost his research position at the Southern University of Science and Technology in China — but now MIT Technology Review, which first broke the news of the experiment back in 2018, reports that he’s out of prison and even answered his cell phone for a brief call.

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Scientists Create Synthetic Organisms That Can Reproduce https://lifeboat.com/blog/2022/04/scientists-create-synthetic-organisms-that-can-reproduce Sun, 03 Apr 2022 15:02:30 +0000 https://lifeboat.com/blog/2022/04/scientists-create-synthetic-organisms-that-can-reproduce

Scientists have created synthetic organisms that can self-replicate. Known as “Xenobots,” these tiny millimeter-wide biological machines now have the ability to reproduce — a striking leap forward in synthetic biology.

Published in the Proceedings of the National Academy of Sciences 0, a joint team from the University of Vermont, Tufts University, and Harvard University used Xenopus laevis frog embryonic cells to construct the Xenobots.

Their original work began in 2020 when the Xenobots were first “built.” The team designed an algorithm that assembled countless cells together to construct various biological machines, eventually settling on embryonic skin cells from frogs.

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Reflections on the ethics of genetic enhancement https://lifeboat.com/blog/2022/02/reflections-on-the-ethics-of-genetic-enhancement Thu, 24 Feb 2022 01:22:35 +0000 https://lifeboat.com/blog/2022/02/reflections-on-the-ethics-of-genetic-enhancement Public policy includes efforts by governmental as well as nongovernmental agencies (other than professional associations) to manage genetic enhancement. For example, the International Olympic Committee has a policy on performance-enhancing drugs in sport. In the United States, the Food and Drug Administration classified synthetic anabolic steroids as a restricted class of drugs, making it more difficult to get access to them. Such measures will not always be successful. Epoetin alfa (EPO) is a useful medication for the many people who suffer from chronic anemia, including people who must undergo regular renal dialysis. As a consequence, it is in very wide supply for legitimate therapeutic purposes, unlike the synthetic anabolic steroids. Imposing strict limitations on access to EPO would create an enormous inconvenience for the large number of people who benefit from the drug. The fact that some athletes are able to get their hands on EPO is an unintended consequence of having the drug widely available for legitimate therapeutic uses. The appropriate public policy will not be the same, necessarily, for every drug.

By “personal policy” we mean the moral understandings and social practices of individuals, parents, and families, including those moral convictions that would cause them to refrain from unwise or unfair use of genetic enhancement technologies. The Worth of a Child, for example, focuses on ethical issues involving children and parents.11 How does one engage that sort of personal policy response? The means we have are limited but powerful: education, public dialogue, and the encouragement of ethical reflection.

In conclusion, there are four points worth reiterating. First, as we think about genetic enhancement, we should use a broad definition of genetic-enhancement technologies, not merely gene manipulation, but indirect genetic technologies, such as biosynthetic drugs. Second, we should try to anticipate the enhancement temptations of new therapies. Such anticipation may help us in shaping the marketing, availability, or other aspects of those technologies. Third, we should promote the adoption of appropriate public and professional policies. Finally, we should provide public education and dialogue to encourage personal ethical reflection on the appropriate uses and limits of genetic-enhancement technologies.

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Jeff Bezos Startup Hires Top Scientist to Defeat Death https://lifeboat.com/blog/2022/01/jeff-bezos-startup-hires-top-scientist-to-defeat-death Fri, 21 Jan 2022 03:23:15 +0000 https://lifeboat.com/blog/2022/01/jeff-bezos-startup-hires-top-scientist-to-defeat-death

Jeff Bezos has backed anti-aging startup Alto Labs, which has recently hired former chief scientific officer of GlaxoSmithKline Hal Barron as its CEO.

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New Virus-Like Particles Can Deliver CRISPR to Any Cell in the Body https://lifeboat.com/blog/2022/01/new-virus-like-particles-can-deliver-crispr-to-any-cell-in-the-body Thu, 20 Jan 2022 08:23:25 +0000 https://lifeboat.com/blog/2022/01/new-virus-like-particles-can-deliver-crispr-to-any-cell-in-the-body

One critical difference? Unlike a Mars mission’s “seven minutes of terror,” during which the entry, descent, and landing occur too fast for human operators to interfere, gene therapy delivery is completely blind. Once inside the body, the entire flight sequence rests solely on the design of the carrier “spaceship.”

In other words, for gene therapy to work efficiently, smarter carriers are imperative.

This month, a team at Harvard led by Dr. David Liu launched a new generation of molecular carriers inspired by viruses. Dubbed engineered virus-like particles (eVLPs), these bubble-like carriers can deliver CRISPR and base editing components to a myriad of organs with minimal side effects.

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