NIAID, DARPA, Bill Gates Intentionally Infect 80 Americans With Lab-Made Pandemic Influenza Virus: HHS Study

A federally run experiment funded by the National Institute of Allergy and Infectious Diseases (NIAID), the Defense Advanced Research Projects Agency (DARPA), and the Bill & Melinda Gates Foundation deliberately infected 80 American adults with a lab-grown pandemic influenza virus at the National Institutes of Health (NIH) Clinical Center in Bethesda, Maryland.

Data from 74 of those infected were analyzed, and 53 of them (72% of analyzed participants, or at least 66% of all infected participants) were confirmed to be shedding the pathogen, meaning they were actively contagious and could infect others.

We do not know whether six participants who were excluded from the study after being deliberately infected were shedding the virus or not.

Regardless, 53 of the individuals became contagious to others.

The human-infection experiment—officially published in Science Translational Medicine (Aug. 2025) under the title “Nasal and systemic immune responses correlate with viral shedding after influenza challenge in people with complex preexisting immunity”—was conducted entirely under the jurisdiction of the U.S. Department of Health and Human Services (HHS).

The original HHS manuscript can be found here: https://pmc.ncbi.nlm.nih.gov/articles/PMC12375958/pdf/nihms-2097372.pdf

Lab-Made Pandemic Virus Used to Infect Humans

According to the paper, participants were “challenged with 107 half-maximal tissue culture infectious dose (TCID50) of a 2009 pandemic H1N1 strain, A/Bethesda/MM2/H1N1.”

That purported virus was not naturally circulating.

It was a lab-engineered clone of the 2009 pandemic influenza A (H1N1) virus, manufactured by NIH scientists in Bethesda and maintained as a standardized “human challenge” stock.

The virus name itself—A/Bethesda/MM2/H1N1—identifies it as an NIH-made strain.

The “Bethesda” designation marks its laboratory origin at NIH’s Maryland facility, and “MM2” denotes the second master-mix batch of the cloned challenge stock.

80 Individuals Deliberately Infected Under HHS Oversight

The study describes the deliberate exposure of 80 adults to this laboratory-made pandemic influenza strain in 2019.

“The challenge study (clinicaltrials.gov NCT01971255) was performed at the NIH Clinical Center between April and October 2019,” the study reads.

Interestingly, that means the 80 human participants were intentionally infected with the NIH-made H1N1 influenza virus roughly five to six months before COVID-19 was first reported in Wuhan, China (December 2019).

So, while the study was published in Science Translational Medicine in August 2025, the actual human infections occurred in mid-2019.

Half of those deliberately infected had been vaccinated roughly two months earlier with a commercial quadrivalent influenza vaccine; the other half had not.

“All 80 participants were brought into the NIH Clinical Center as mixed cohorts and challenged with 107 TCID50 of influenza A/Bethesda/MM2/H1N1 virus … and assessed daily for a minimum of 9 days.”

Although only 74 participants were ultimately included in the analysis (after six were excluded), every one of them was intentionally inoculated with a live, replication-competent pandemic virus.

The experiment was run on U.S. federal property by U.S. government scientists.

It was approved by the NIAID Institutional Review Board (IRB No. 19-I-0058), making it an officially sanctioned HHS human-infection study.

The human infection experiment was carried out under a multi-million U.S. taxpayer dollar project titled “Universal Influenza Vaccine Development” (project number 1ZIAAI001372), led by Dr. Jeffery Taubenberger.

Dr. Taubenberger—listed as an author on the study—is the current NIAID Director, taking over Anthony Fauci’s spot.

Taubenberger holds a patent for the carcinogenic BPL technology at the center of the Trump administration’s new ’Generation Gold Standard’ influenza bird flu pandemic vaccine platform.

His agency is also directing U.S. tax dollars to fund the creation of never-before-seen “Frankenstein” bird flu viruses.

Confirmed 72% of Analyzed Participants—& at Least 66% of All Infected—Became Infectious

A total of 80 volunteers were deliberately infected with the NIH-made influenza virus, but data from only 74 participants were included in the final published analysis.

Among those 74 analyzed participants, 53 were confirmed to actively shed virus, meaning they were contagious.

Because the six excluded individuals were not evaluated for viral shedding, the true number of infectious participants could be higher, but only 53 are confirmed in the published dataset.

That equates to 72% of the analyzed group and at least 66% of everyone infected becoming contagious, some for several days.

Shedding was tracked by daily nasal swabs using the BioFire Respiratory Pathogen Panel and qRT-PCR testing for the influenza M gene.

Participants were considered “shedding” when viral RNA was detected in nasal-wash samples.

“[P]articipants shedding virus for two or more days showed higher early viral loads and exhibited stronger induction of antiviral responses compared with participants who shed virus for one day.”

The highest viral loads appeared in multiday shedders on days 1–3 post-infection, coinciding with the most severe flu-like symptoms, as measured by NIH’s FluPro symptom scoring system.

Vaccination Failed to Prevent Infection or Shedding

Vaccination did not prevent infection.

The paper admits that “vaccinated shedders” displayed increased T-cell activity and inflammatory markers, including CD8A, PD-L1, IFN-?, IL-6, and TNF-ß, compared to unvaccinated shedders—indicating that vaccination did not stop infection but instead triggered a hyper-inflammatory immune response.

Females were three times more likely to clear the infection after only one day of shedding, while males were more likely to shed virus for multiple days.

Funding: NIAID, DARPA, and Gates Foundation

The study lists its financial backers as:

NIAID Intramural Research Program (grants AI000986-12 and AI001157-07)

DARPA (Defense Advanced Research Projects Agency), contract HR0011831160

Bill & Melinda Gates Foundation, grant OPP1178956

That combination of government and private funders represents the same triad—HHS, the Pentagon, and the Gates Foundation—responsible for many dual-use biological and “pandemic preparedness” programs that blur the line between public health and bio-defense research.

Containment & Biosafety Measures Not Disclosed

Remarkably, the 2025 Science Translational Medicine paper and HHS manuscript provide no description whatsoever of biosafety precautions—no mention of negative-pressure rooms, isolation conditions, or post-infection quarantine protocols to prevent secondary transmission.

Readers of the study are unable to verify how the government prevented infected subjects from spreading the lab-made virus to others, raising national security concerns.

It further raises grave informed-consent concerns, as individuals who interacted with these infected volunteers beyond the study setting were never informed that they might be exposed to an NIH-made pandemic influenza virus.

Given that 72 percent of participants were confirmed viral shedders, this omission raises serious biosafety and public-transmission concerns.

Conducted Entirely Under HHS Authority

The trial was hosted, funded, staffed, and overseen by HHS agencies from start to finish:

Conducted at the NIH Clinical Center in Bethesda, Maryland

Run by the NIAID Laboratory of Infectious Diseases

Reviewed by an HHS Institutional Review Board

Carried out under HHS Good Clinical Practice guidelines

In short, the U.S. Department of Health and Human Services infected 74 American adults with a lab-grown pandemic influenza virus to study viral shedding and immune-system responses—while omitting basic transparency about containment.

The nation’s top health agency is infecting Americans with pandemic-grade pathogens.

Bottom Line

The federally directed experiment—funded by NIAID, DARPA, and the Bill & Melinda Gates Foundation—was a live human-infection challenge using a lab-engineered influenza strain created by NIH scientists in Bethesda.

Eighty adults were deliberately infected with the laboratory-made pandemic H1N1 virus; data from 74 were analyzed, and 53 of them (72 % of those analyzed, or at least 66 % of everyone infected) were confirmed to be shedding the pathogen—actively contagious and capable of transmitting it to others.

The six excluded participants were also infected, but the government provided no data indicating whether they shed virus, leaving the full extent of contagiousness unknown.

No description was provided for biosafety controls, isolation conditions, or post-infection release criteria, meaning the public record offers no verification of how HHS prevented the spread of its own lab-created virus beyond the NIH facility.

This omission raises not only national-security concerns but also informed-consent violations, since people who may have interacted with participants outside the study were never notified of possible exposure to an NIH-made pathogen.

Although the paper frames the experiment as advancing “next-generation vaccine development,” its findings instead showed that vaccination failed to prevent infection or viral shedding and appeared to trigger immune hyperactivation in vaccinated participants.

The newly published HHS study therefore stands as a rare, fully documented example of the U.S. Department of Health and Human Services deliberately infecting American citizens with a laboratory-grown pandemic-grade virus—underwritten by HHS, DARPA, and the Gates Foundation, with no transparent account of how the resulting contagion was contained.

Finish reading: https://open.substack.com/pub/jonfleetwood/p/niaid-darpa-bill-gates-intentionally

Your Risk Of Dying From The Vaccine Far Exceeds Your Risk Of Death From The Disease

Risk Of Death From Vaccine Greater Than Risk Of Death From Disease

“Unequivocally…For Every Single Vaccine On The Childhood Schedule…Your Risk Of Dying From The Vaccine Far Exceeds Your Risk Of Death From The Disease.”
Dr Paul Thomas, MD

“If You’re Afraid Of Your Child Dying, If That’s What You Fear The Most…Do Not Give Them A Vaccine.”

Full Data—Rounded For Ease Of Reference… Unrounded Raw Data Listed At Bottom Of Post.
Polio:
Death From The Disease: 1 in 1 Trillion
Death From The Vaccine: 1 in 215K

Diphtheria:
Death From The Disease: 1 in 42.5 Million
Death From The Vaccine: 1 in 76K

Tetanus:
Death From The Disease: 1 in 1.5 Million
Death From The Vaccine: 1 in 76K

Pertussis:
Death From The Disease: 1 in 2.3 Million
Death From The Vaccine: 1 in 76K

Measles:
Death From The Disease: 1 in 106.5 Million
Death From The Vaccine: 1 in 108K

Mumps:
Death From The Disease: 1 in 40.3 Million
Death From The Vaccine: 1 in 108K

Rubella:
Death From The Disease: 0/ Negligible
Death From The Vaccine: 1 in 108K

Varicella:
Death From The Disease: 1 in 32.3 Million
Death From The Vaccine: 1 in 202K

Hepatitis A:
Death From The Disease: 1 in 1.6 Million
Death From The Vaccine: 1 in 73K

Hepatitis B:
Death From The Disease: 1 in 305K
Death From The Vaccine: 1 in 96K

HIB:
Death From The Disease: 1 in 1.5 Million
Death From The Vaccine: 1 in 46K

Pneumococcal:
Death From The Disease: 1 in 236K
Death From The Vaccine: 1 in 50K

Meningococcal:
Death From The Disease: 1 in 822K
Death From The Vaccine: 1 in 141K

Influenza:
Death From The Disease: 1 in 136K
Death From The Vaccine: 1 in 15K

Dr. Paul Thomas, Dr. Kenneth P. Stoller & Stand for Health Freedom, are suing the CDC. The lawsuit accuses the CDC of recommending 72+ vaccine doses for American children without ever testing the cumulative schedule for safety.

The Lawsuit…
No safety testing: The CDC & FDA has never studied the long term, combined effects of the full childhood schedule. The Institute Of Medicine has issued two decades of warnings, but no accountability or action has resulted.

27 years of silence: By law, HHS must file biennial reports to Congress on vaccine safety efforts. No reports have been issued since 1998.

Constitutional violations: The suit charges the CDC with First Amendment violations(silencing dissenting doctors), the Fifth Amendment violations(due process & bodily integrity) & the Administrative Procedure Act violations(arbitrary & capricious rulemaking).

The Plaintiffs Seek…
Reclassification of all childhood vaccines to Category B. This shifts to shared decision making, which would make medical exemptions far easier to obtain.

That rigorous safety studies be required, comparing fully vaccinated vs. unvaccinated children before any return to a mandated schedule.

To end retaliation against doctors. Physicians who issue exemptions based on individualized medical judgment, would be protected.

If the case is won, this lawsuit will expose the unlawful CDC hyper vaccination program. It will mark a massive victory for families who seek vaccine exemptions & for physicians fighting to practice real ‘patient focused’ medicine.

Full Raw Data—‘Unrounded’ Complete Numbers…
POLIO: Risk of death from Polio is 1 in 1 Trillion. Risk of death from the Polio Vaccine is 1 in 214,973.

DIPHTHERIA: Risk of death from Diphtheria is 1 in 42,509,839. Risk of death from the DTaP Vaccine is 1 in 76,341.

TETANUS: Risk of death from Tetanus is 1 in 1,506,184. Risk of death from the DTaP Vaccine is 1 in 76,341.

PERTUSSIS: Risk of death from Pertussis is 1 in 2,346,718. Risk of death from the DTaP Vaccine is 1 in 76,341.

MEASLES: Risk of death from Measles is 1 in 106,506,429. Risk of death from the MMR Vaccine is 1 in 108,666.

MUMPS: Risk of death from Mumps is 1 in 40,371,594. Risk of death from the MMR Vaccine is 1 in 108,666.

RUBELLA: Risk of death from Rubella is 0. Risk of death from the MMR Vaccine is 1 in 108,666.

VARICELLA: Risk of death from Chickenpox is 1 in 32,331,860. Risk of death from the Vaccine is 1 in 202,398.

HEPATITIS A: Risk of death from Hepatitis A is 1 in 1,667,135. Risk of death from the Vaccine is 1 in 72,948.

HEPATITIS B: Risk of death from Hepatitis B is 1 in 305,465. Risk of death from the vaccine is 1 in 96,314.

HIB: Risk of death from HIB is 1 in 1,494,710. Risk of death from the HIB Vaccine is 1 in 45,966.

PNEUMOCOCCAL: Risk of death from Pneumonia is 1 in 236,562. Risk of death from the vaccine is 1 in 50,056.

MENINGOCOCCAL: Risk of death from Meningitis is 1 in 821,925. Risk of death from the Vaccine is 1 in 141,124.

INFLUENZA: Risk of death from Influenza is 1 in 135,905. Risk of death from the Flu Vaccine is 1 in 15,702.

Dr Paul Thomas, MD “Vax Facts”
https://a.co/d/h2HLWEk

Stand For Health Freedom
https://standforhealthfreedom.com

Dr Paul Thomas’ Research Data
https://doctorsandscience.com/presentations.html

Speaker:
@Paulthomasmd

Video: @toxins_in_children

Click to view the video: https://x.com/ValerieAnne1970/status/1977615087847321647

Deadly Cancer-Causing Chemical ‘BPL’ at Center of $500 Million Pandemic Bird Flu Vaccine Platform

Atomic Structure

The chemical used in the Trump administration’s new ‘Generation Gold Standard’ bird flu vaccine platform—beta-propiolactone (BPL)—is classified as a ‘Group 2B’ carcinogen by U.S. regulators (meaning the substance is possibly cancer-causing in humans) and as a ‘Group 1B’ carcinogen in Europe (meaning it’s presumed to cause cancer in humans).

A carcinogen is any substance or agent capable of causing cancer by damaging a cell’s DNA and leading to uncontrolled cell growth.

The revelation follows this website’s report that the U.S. National Institute of Allergy and Infectious Diseases (NIAID)—under Dr. Jeffery Taubenberger’s direction—has been funding the creation of chimeric, lab-engineered bird flu viruses in American and foreign laboratories, even as Taubenberger himself is named on a federal patent for the very BPL-utilizing bird flu vaccine platform those experiments are designed to justify.

A May 2025 government press release announced the multi-million dollar BPL platform will be used to generate bird flu pandemic vaccines:

The U.S. Department of Health and Human Services (HHS) and the National Institutes for Health (NIH) today announced the development of the next-generation, universal vaccine platform, Generation Gold Standard, using a beta-propiolactone (BPL)-inactivated, whole-virus platform.

This initiative represents a decisive shift toward transparency, effectiveness, and comprehensive preparedness, funding the NIH’s in-house development of universal influenza and coronavirus vaccines, including candidates BPL-1357 and BPL-24910. These vaccines aim to provide broad-spectrum protection against multiple strains of pandemic-prone viruses like H5N1 avian influenza and coronaviruses including SARS-CoV-2, SARS-CoV-1, and MERS-CoV.

https://open.substack.com/pub/jonfleetwood/p/deadly-cancer-causing-chemical-bpl

Ivermection Reduces Tumours

Ivermection Reduces Tumours

Another ivermectin study is out, and like the long list of similar studies lately, it shows more cancer treatment potential. This one was published in July in ACS Biomaterials Science, titled, “Intranasal Delivery of Ivermectin Nanosystems as an Antitumor Agent: Focusing on Glioma Suppression.”

In short, the study found low-dose ivermectin shrank brain tumors by a whopping 70% in rats. The treated rodents also had less dead tissue, less swelling, and fewer new blood vessels forming, which means the remaining tumors were less invasive and less aggressive.

The ivermectin was delivered using a nasal spray in a very fine (nanoscale) form, since oral ivermectin can’t cross the blood-brain barrier. The rats that got the treatment showed no negative side effects.

The serendipitous discovery of ivermectin is one of the most remarkable stories in medical science. In the 1970s, Japanese microbiologist Satoshi Omura set out to find new microorganisms that might produce useful medicines. He collected hundreds of soil samples from around Japan, including one from a golf course in Kawana, south of Tokyo.

In one of his golf-course soil samples, Omura’s team isolated a previously unknown bacterium that produced compounds found to be extraordinarily effective at killing parasitic worms. He sent it to a U.S. lab at Merck, which developed ivermectin: a safer and even more potent chemical derivative of the bacterial compound.

As you know, in 2015, Omura and Merck researcher Bill Campbell jointly received the Nobel Prize in Medicine for a cheap dirt drug that has saved millions from disease and blindness. If ivermectin’s cancer-fighting abilities bear out —and the studies and anecdotes keep mounting up— it will become the single most beneficial accidental discovery in human history.

Here’s a question to ponder: would ivermectin have broken out of the pharma wilderness absent its high-profile role during the pandemic as a cultural and political flashpoint? Without this extraordinary exposure, efforts to study ivermectin as a cancer agent would almost certainly have remained niche— buried in the literature amid hundreds of other “drug repurposing” efforts, lacking funding, conference time, or media coverage.

Ivermectin may wind up being the greatest covid miracle of all.

https://open.substack.com/pub/coffeeandcovid/p/dizzying-dichotomies-saturday-october

Overview Of The Fertility Impacts Of COVID Vaccines

The jump in miscarriages/stillbirths with vaccine uptake.

Miscarriages/Stillbirths Post VaccineThe correlation of injection to fetal death showed very tight timing, with by far the most fetal deaths occurring the same day.

Stillbirths Post Covid Vaccine

And for guys…

The likely mechanism of reduced sperm production is that both spermatogonia and spermatozoa, as well as their support cells, Leydig and Sertoli cells, all abundantly express the ACE2 receptor and various TMPRSS and furin proteases, all of which attach the spike protein, and this has been known since 2020. Those cells are all in the testicles, which the Pfizer-Acuitas study found to receive the mRNA vaccine content within minutes.

Sperm are dependent for their survival and function on the participation of ACE2 in the angiotensin system. When the spike protein attaches to the ACE2 receptor, which it specifically targets, it cleaves the latter, rendering the sperm non-viable.

Read more: https://open.substack.com/pub/colleenhuber/p/overview-of-fertility-impacts-of

On Poisoning: Lead vs. The Spike Protein: Both Parallel Each Other In How They Poison Us

We have heard it over and over: The COVID mRNA gene therapies are poison. Many have scoffed at this claim, most notably governing medical agencies. However, when you take the time to look at the mechanisms at work, the claim is not far-fetched – at all. Let’s dive into how lead and the spike protein poison the body in similar ways.

https://open.substack.com/pub/wmcresearch/p/on-poisoning-lead-vs-the-spike-protein