Human-animal hybrids: Senate approves billions of dollars for their chilling creation

Jose Hermosa – June 15, 2021

After a long debate, The Senate approved with 68–32 votes a budget of $250 billion to continue with the controversial creation of hybrid beings by mixing human and animal genetic material.

The bill called the “Endless Frontier Act,” was introduced by Senate Majority Leader Chuck Schumer, D-New York, according to Life Site on June 14.

Sen. James Lankford (R-Okla.) referred to the ethical incompatibility and the need to establish clear definitions on the matter in an attitude of submission to international competition.

“We shouldn’t need to clarify in law that creating animal-human hybrids or ‘chimeras’ is ethically unthinkable, but sadly the need for that very clear distinction has arrived,” said Lankford, who, along with Sens. Mike Braun R-Ind.), and Steve Daines (R-Mont.) sought to criminalize the creation of such creatures.

He added: “There’s a real difference in taking human cells and injecting them into a mouse for cancer research and for other research. That’s been done, and it’s been done for a very long time, and we’ve had time to be able to process that, but trying to be able to create life is a very different threshold for me.”

Senator Daines noted, “In trying to compete with China, we shouldn’t become like them, It’s critical that we draw a bright line against unethical forms of research that fail to recognize the distinct value of humans over animals.”

Although the 2019 Trump Administration had shut down the procurement of human fetal tissue from elective abortions for research and created an ethics board to review any such research in laboratories and universities, the National Institutes of Health (NIH) reversed these provisions in April 2021.

On the other hand, private research at U.S. universities continues its experiments.

https://m.thebl.tv

Biden Admin Clears The Way To Allow Research On Fetal Tissue From Abortions

Charlotte Pence Bond – April 16, 2021

On Friday, the Biden administration announced the removal of a previous barrier that restricted certain kinds of research conducted on fetal tissue from elective abortions.

The National Institutes of Health (NIH) released a statement on Friday saying that it was undoing some of the previous administration’s policies regarding research conducted on fetal tissue gathered from abortions.

The statement said that the Department of Health and Human Services (HHS) is “reversing its 2019 decision that all research applications for NIH grants and contracts proposing the use of human fetal tissue from elective abortions will be reviewed by an Ethics Advisory Board.” It added that another Human Fetal Tissue Research Ethics Advisory Board will not be created.

The statement noted: “NIH reminds the community of expectations to obtain informed consent from the donor for any NIH-funded research using human fetal tissue … and of continued obligations to conduct such research only in accord with any applicable federal, state, or local laws and regulations, including prohibitions on the payment of valuable consideration for such tissue.”

During a hearing at the House of Representatives on Thursday, HHS Secretary Xavier Becerra discussed the changes prior to the official announcement, as reported by Politico.

“We believe that we have to do the research it takes to make sure that we are incorporating innovation and getting all of those types of treatments and therapies out there to the American people,” he said.

Pro-life groups have spoken out against the measure, saying that the topic would be a main issue in the midterm elections next year, the outlet reported.

https://www.dailywire.com

New deadly disease dubbed VEXAS gives men fevers, blood clots, and inflammation

Strange Sounds – October 28, 2020

There are likely hundreds of men in the United States, if not more, who suffer from a just-discovered genetic disease that causes symptoms including blood clots in veins, recurrent fevers, lung system abnormalities, and — in 40% of patients — death. 

Researchers from the National Institutes of Health discovered the disease, named VEXAS, by working backwards: Rather than grouping people with similar symptoms and searching for biological explanations, they searched the genetic makeup of 2,500 people for variations that could be linked to the wide-ranging symptoms of their undiagnosed inflammatory conditions.

We had many patients with undiagnosed inflammatory conditions who were coming to the NIH Clinical Center, and we were just unable to diagnose them,” said Dr. David B. Beck, clinical fellow at NHGRI and lead author of the paper.

That’s when we had the idea of doing it the opposite way. Instead of starting with symptoms, start with a list of genes. Then, study the genomes of undiagnosed individuals and see where it takes us.

Using that method, the scientists eventually identified three middle-aged men who all had the same mutations in a gene called UBA1. They later discovered 22 other men with the same mutations and similar symptoms, like blood clots and fevers.

The research team named the disease VEXAS after its key characteristics: vacuoles (unusual cavity-like structures in certain cells), E1 enzyme (which is related to UBA1), X-linked (per the chromosome it’s connected to), autoinflammatory (meaning the immune system accidentally attacks the body) and somatic (since the condition seems ot pop up sometime during the patient’s life, rather than at birth).

The researchers suspect VEXAS has only been found in men because it’s linked to the X chromosome, of which men only have one. Women’s additional X chromosome, they hypothesize, could be protective in this case.

https://strangesounds.org

Scientists discover ‘devastating’ NEW genetic disease that’s killed 40% of known patients by attacking lungs and immune system

RT – November 1, 2020

The new condition, which is caused by genetic mutations, has shown a particularly high death rate, as patients were not responding to any currently available treatments, the researchers said.

The disease – ‘vacuoles, E1 enzyme, X-linked, autoinflammatory and somatic syndrome’ – has been dubbed VEXAS. It causes symptoms that include blood clots in veins, recurrent fevers, abnormalities in the lungs, and vacuoles – unusual cavity-like structures – in the myeloid cells, which play a crucial part in the human immune system.

Researchers at the US National Institutes of Health (NIH) came across the disease after analyzing the genome sequences of more than 2,500 people with undiagnosed inflammatory diseases. In comparing the data, they found that 25 adult males had particular mutations in the UBA1 gene, which is believed to be the source of VEXAS.

“Instead of looking at clinical similarities, we were instead taking advantage of shared genomic similarities that could help us discover a completely new disease,” said Daniel Kastner, the scientific director of the Intramural Research Program at the National Human Genome Research Institute.

The NIH reported that the new disease “can be life-threatening,” as 40 percent of the VEXAS patients the researchers studied have died. The high death toll revealed “the devastating consequences of the severe condition,” the team stated.

Kastner told NBC News that patients with VEXAS become “really sick,” and “don’t respond to any treatments, from high doses of steroids to various chemotherapies.”

https://www.rt.com