Anonymous ID: 1947ca Nov. 24, 2022, 10:36 a.m. No.17805249   🗄️.is 🔗kun   >>5258 >>5340 >>5346 >>5350 >>5375 >>5458

>>17805213 (lb)

5G & 6G.

invisible containment, active denial systems, remote cardiac failure triggering, etc…

 

Nanometals = conductivity increase. (M)antennas

 

Recall King Charles last year calling for a military stylee campaign against climate change at COP26?

 

Bio/nano weapons, weather technology, propaganda, human and livestock germs, and microwave technology would all be correctly considered military weapons platforms… and humans are the carbon they wish to reduce.

 

Also remember Trump saying something like " 5G, 6G, and beyond"…

Anonymous ID: 1947ca Nov. 24, 2022, 11:22 a.m. No.17805356   🗄️.is 🔗kun   >>5367 >>5375 >>5440 >>5458

>>17805326

> treatments is what killed them

and know the vaxed all have VAIDS/ADE.

 

https://www.nih.gov/news-events/news-releases/nih-launches-clinical-trial-three-mrna-hiv-vaccines

 

NIH launches clinical trial of three mRNA HIV vaccines

Phase 1 study is among first to examine mRNA technology for HIV.NIH launches clinical trial of three mRNA HIV vaccines

 

Phase 1 study is among first to examine mRNA technology for HIV.

 

The National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health, has launched a Phase 1 clinical trial evaluating three experimental HIV vaccines based on a messenger RNA (mRNA) platform—a technology used in several approved COVID-19 vaccines. NIAID is sponsoring the study, called HVTN 302, and the NIAID-funded HIV Vaccine Trials Network (HVTN), based at Fred Hutchinson Cancer Research Center in Seattle, is conducting the trial.

 

“Finding an HIV vaccine has proven to be a daunting scientific challenge,” said Anthony S. Fauci, M.D. NIAID director. “With the success of safe and highly effective COVID-19 vaccines, we have an exciting opportunity to learn whether mRNA technology can achieve similar results against HIV infection.”

 

An mRNA vaccine works by delivering a piece of genetic material that instructs the body to make a protein fragment of a target pathogen (such as a virus), which the immune system recognizes and remembers, so it can mount a substantial response if later exposed to that pathogen. The HVTN 302 study will examine whether the following three experimental HIV mRNA vaccines are safe and can induce an immune response: 1) BG505 MD39.3 mRNA, 2) BG505 MD39.3 gp151 mRNA, and 3) BG505 MD39.3 gp151 CD4KO mRNA. Each investigational vaccine candidate is designed to present the spike protein found on the surface of HIV that facilitates entry into human cells. Each of the experimental vaccines encodes for different but highly related, stabilized proteins. None of the three vaccine candidates can cause HIV infection.

 

The specific mRNA sequences contained in the vaccines were designed and developed by investigators at the NIAID-funded Scripps Consortium for HIV/AIDS Vaccine Development (CHAVD) at the Scripps Research Institute and the Bill & Melinda Gates Foundation-funded IAVI Neutralizing Antibody Center at Scripps, in collaboration with scientists at Cambridge, Massachusetts-based Moderna, Inc. Moderna manufactured the investigational vaccines through a NIAID-supported contract.

 

Led by principal investigators Jesse Clark, M.D., of the University of California Los Angeles, and Sharon Riddler, M.D., of the University of Pittsburgh, the HVTN 302 study will enroll up to 108 adults ages 18 to 55 years at 11 sites in: Birmingham, Alabama; Boston; Los Angeles; New York City; Philadelphia; Pittsburgh; Rochester, New York and Seattle. Each participant will be randomly assigned to one of six groups each receiving three vaccinations of one of the experimental vaccines. The first three groups (18 participants each), called Group A, will receive intramuscular injections of 100 micrograms (mcg) of their assigned vaccine candidate at the initial visit, at month two and again at month six. Participants in Group A will be evaluated two weeks after initial vaccination to ensure safety criteria have been met. If so, the remaining three groups of 18 participants each (Group B) will be vaccinated with 250 mcg of the assigned investigational vaccine, followed by injections two and six months after the initial vaccination.

 

Safety and immune responses will be examined via blood and lymph node fine-needle aspiration samples taken at specified timepoints throughout the trial. Clinical staff will closely monitor participant safety throughout the study. The clinical trial is expected to be completed by July 2023.

 

More information about the HVTN 302 study is available on ClinicalTrials.gov using the identifier NCT05217641.

Anonymous ID: 1947ca Nov. 24, 2022, 11:43 a.m. No.17805400   🗄️.is 🔗kun

>>17805315

Good idea, but how does it help those who will see it (assuming they are vaxxed) from also Dying Suddenly? It might even expedite it, as it will me a stress/anger/cortisol/heart overload for many of those who 'get it'.