2015: VACCINES, RETROVIRUSES, DNA, AND THE DISCOVERY THAT DESTROYED JUDY MIKOVITS’ CAREER

http://www.blacklistednews.com/2015%3A_Vaccines%2C_Retroviruses%2C_DNA%2C_and_the_Discovery_that_Destroyed_Judy_Mikovits’_Career/61017/0/38/38/Y/M.html
[size=35]2015: VACCINES, RETROVIRUSES, DNA, AND THE DISCOVERY THAT DESTROYED JUDY MIKOVITS’ CAREER[/size]
Published: September 27, 2017

SOURCE: ORGANIC LIFESTYLE MAGAZINE

Judy Mikovits, PhD is a biochemist and molecular biologist with more than 33 years of experience. Internationally known, a veritable “rock star” of the scientific world, she served as the director of the lab of Antiviral Drug Mechanisms at the National Cancer Institute before directing the Cancer Biology program at EpiGenX Pharmaceuticals. She later developed the first neuroimmune institute. Her early work focused on cancer and HIV, her latest on Chronic Fatigue Syndrome and autism. She has published more than 50 peer-reviewed articles.
In 2011, she made the discovery that destroyed her career. She found that at least 30% of our vaccines are contaminated with gammaretroviruses. Not only is this contamination associated with autism and chronic fatigue syndrome, it is also associated with Parkinson’s, Lou Gehrig’s disease, and Alzheimer’s.
When she released this shocking information, she was warned by Dr. Andrew Wakefield that she would become a target, just as he had been. But she assured him that all of her work had been properly reviewed and, of course, she was safe.
She was wrong. She was threatened and told to destroy her data; she refused. She was fired, then arrested for supposedly stealing her data from her worksite. She had been facing charges and was bound by a gag order from the court for the last four years. Recently, charges were dropped and the gag order was lifted. Dr. Mikovits is now free to talk, and boy is she talking.
The retroviruses contaminating vaccines originate from mice used for research. Dr. Mikovits asks, “How many new retroviruses have we created through all the mouse research, the vaccine research, gene therapy research? More importantly, how many new diseases have we created?”
“When they destroyed all of our work, and discredited everything I or Frank Ruscetti had ever published, and arranged for the publication of my mug shot in Science, the NIH very deliberately sent the message to researchers everywhere about what would happen to any honest scientist who dared ask those important questions.”

https://fellowshipoftheminds.com/2017/09/27/new-study-finds-aluminum-in-vaccines-triggers-autism-esp-in-boys/

New study finds aluminum in vaccines triggers autism, esp. in boys
Posted on September 27, 2017 by Dr. Eowyn | 10 Comments
Despite the MSM and the medical establishment’s demonization of vaccine skeptics (see “Baylor U. professor & M.D. Carol Baker: ‘Let’s just get rid of all the whites in the United States’ (includes discussion on enforcing childhood vaccination, we actually do have compelling evidence of the deleterious effects of vaccines. See:

• Flu vaccine linked to significantly higher rate of miscarriages
  
  
• HPV vaccines have infertility side-effects
  
  
• CDC admits millions of Americans given cancer virus via polio vaccine
  
  
• Some thoughts on the globalist agenda, vaccines and population control
  
  
• German government officials get ‘safer’ vaccines
  
  
• Aborted human fetal cells in your food, vaccines, and cosmetics
  
  

Particularly troubling is the association of childhood vaccination and autism. See:

• New study finds link between child vaccination and autism – CENSORED
  
  
• It’s not paranoia: Maker of DTaP vaccine admits it causes autism
  
  
• Physicians say aborted human fetal cells used for measles vaccine may cause autism
  
  

Now, a new study has pinpointed the aluminum in vaccines as the agent in triggering autism, especially in boys.
The study was conducted by a team of four scientists at the University of British Columbia in Vancouver, BC, Canada:

• Dan Li, Dept. of Ophthalmology and Visual Sciences.
  
  
• Lucija Tomljenovic, Dept. of Ophthalmology and Visual Sciences.
  
  
• Yongling Li,  Dept. of Ophthalmology and Visual Sciences.
  
  
• Christopher A. Shaw, Dept. of Ophthalmology and Visual Sciences, Program in Experimental Medicine, and Program in Neuroscience.
  
  

The four scientists reported their findings in an article titled, “Subcutaneous injections of aluminum at vaccine adjuvant levels activate innate immune genes in mouse brain that are homologous with biomarkers of autism,” in the peer-reviewed Journal of Inorganic Biochemistry, Volume 177, December 2017, pp. 39-54.
Here’s a summary of the study:

• Vaccines contain aluminum adjuvant — a pharmacological agent added to a drug to increase or aid its effect.
  
  
• The scientists injected aluminum into mice.
  
  
• The aluminum had neuro-inflammatory effects on the mice’s frontal cortex.
  
  
• The frontal cortex is  involved in emotional and social functions which are impaired in autism.
  
  
• Male mice are especially susceptible to aluminum’s neuro-toxic effects.
  
  

ABSTRACT

Quote :

Autism is a neurobehavioral disorder characterized by immune dysfunction. It is manifested in early childhood, during a window of early developmental vulnerability where the normal developmental trajectory is most susceptible to xenobiotic insults. Aluminum (Al) vaccine adjuvants are xenobiotics with immunostimulating and neurotoxic properties to which infants worldwide are routinely exposed. To investigate Aluminum′s immune and neurotoxic impact in vivo, we tested the expression of 17 genes which are implicated in both autism and innate immune response in brain samples of Aluminum-injected mice in comparison to control mice. Several key players of innate immunity, such as cytokinesCCL2, IFNG and TNFA, were significantly upregulated, while the nuclear factor-kappa beta (NF-κB) inhibitor NFKBIB, and the enzyme controlling the degradation of the neurotransmitteracetylcholine (ACHE), were downregulated in Aluminum-injected male mice. Further, the decrease of the NF-κB inhibitor and the consequent increase in inflammatory signals, led to the activation of the NF-κB signaling pathway resulting in the release of chemokineMIP-1A and cytokines IL-4 and IL-6. It thus appears that Aluminum triggered innate immune system activation and altered cholinergicactivity in male mice, observations which are consistent with those in autism. Female mice were less susceptible to Aluminum exposure as only the expression levels of NF-κB inhibitor and TNFA were altered. Regional patterns of gene expression alterations also exhibited gender differences, as frontal cortex was the most affected area in males and cerebellum in females. Thus, Aluminum adjuvant promotes brain inflammation and males appear to be more susceptible to Aluminum′s toxic effects.

GRAPHICAL ABSTRACT

Quote :

Upon peripheral injection, aluminum activates the nuclear factor-kappa beta (NF-κB) pathway in the brain, resulting in the release of proinflammatory molecules. The increased immunoinflammatory signal downregulates the activity of acetylcholinesterase to activate acetylcholine-mediated immunosuppression. If immunosuppression is not achieved, the excessive immunoinflammatory response may impair neurodevelopmental processes producing autistic pathology.

Some other observations from the article:

• Aluminum is an environmental toxin with demonstrated negative impact on human health, especially the nervous system, to which humans are regularly exposed.
  
  
• Aluminum can enter the human body through various sources including food, drinking water, many infant formulas, cosmetic products, cooking utensilsand pharmaceutical products including antacids and vaccines.
  
  
• Why aluminum in vaccines is particularly toxic: Compared to dietary aluminum of which only ~ 0.25% is absorbed into systemic circulation, aluminum from vaccines is poorly excreted by the body and may be absorbed at over 50% efficiency in the short term and at nearly 100% efficiency long-term. Thus, vaccine-derived Al has a much greater potential to produce toxic effects in the body than that obtained through diet.
  
  
• Aluminum in vaccines affect other body organs, not just the brain: In a series of experiments, a French group found that aluminum injected in vaccine-relevant amounts into 8–10 week old mice (mimicking the amount that adult humans receive through vaccinations) is able to travel to distant organs including the spleen and the brain, where it can be detected one year after injection.
  
  
• Furthermore, aluminum not just damages specific body organs, it triggers the body’s “systemic inflammatory responses.”
  
  
• Even dietary aluminum is deleterious, shown to accumulate in our central nervous system over time, resulting in Alzheimer’s type disease. Aluminum’s neurotoxic effect has also been observed in experimental animals fed equivalent amounts of aluminum to what humans consume through a typical Western diet.
  
  

The study concludes:

Quote :

Altogether, these observations show that the adjuvant form of Aluminum has a unique potential to induce neuroimmune disorders, including those of the autism spectrum.
Given that infants worldwide are regularly exposed to Aluminum adjuvants through routine pediatric vaccinations, it seemed warranted to reassess the neurotoxicity of Aluminum in order to determine whether Aluminum may be considered as one of the potential environmental triggers involved in ASD (autism spectrum disorders).

You can read/download the entire article in PDF format here.
~Eowyn