Vaccine and Autism- a New Scientific Review
Summary of previous Journal of Immunology
Autism and Resulting Medical Conditions
Mercury, Vaccines, and Autism
Impact of environmental factors on the prevalence of autism disorder after 1979
Influence of pediatric vaccines on amygdala growth
Delayed acquisition of neonatal reflexes in newborn primates receiving a thimerosal-containing hepatitis B vaccine
Effect of thimerosal on the neurodevelopment of premature rats
Vaccine World Summit
Nanomolar aluminum induces expression of the inflammatory systemic biomarker C-reactive protein (CRP) in human brain microvessel endothelial cells
"For example, just 10 nM added aluminum (sulfate) to the hBMEC cells increased CRP in the external medium 4-fold" 10nM of aluminum is roughly 27nano grams of aluminum and as you can see here with 27 nano grams of aluminum they show crp increases (markers of inflammation) there are 250MICRO grams of alumthe average vaccine meaning there is roughly 1000-10000 times the amount shown here to cause inflammation is the average vaccine
Toby RogersFlarend et al, source detected Al adjuvant in the brain, kidneys, spleen, liver, lymph nodes and heart. and found that most aluminum was retained in rabbits, even after 28 days - unlike the argument brought forward by Oxford Vaccine Group source which use to argue (in archives) that aluminum was excreted "in a few days", now thanged their wording to "gradually" Movsas Et Al, observed that "No significant change in levels of urinary or serum aluminum were seen after vaccination" - which prompts the question: where did the aluminum go? It was retained in the body, and also possibly through inflammatory granulomas at injection site. To be more specific, in the Flarend study - only about 6% (of Al hydroxide) or 22% (of Al phosphate) is eliminated in urine. Most aluminum adjuvant was retained in the body 1 month after injection been a while since i read these lol Also theres a specific mechscussed in other papers, on how Al adjuvant nanoparticles reach the brain this paper exposes a culture of monocytes (which eventually become macrophages) to Al Adjuvant (in vitro) - now one may argue, that macrophages inside the body may behave differently, which is a reasonable argument. There are other papers below, which rebut this argument. source "Following the injection of AlOOH-containing vaccine in vivo, mfiltrated macrophages bear crystalline inclusions of aluminum hydroxide. We assessed the presence of such inclusions in AlOOH-treated macrophages in vitro. By electron microscopy, we observed numerous, large crystalline inclusions in macrophages treated for 2 days with AlOOH (Fig. 2B and C), very similar to those observed in vivo" source and this paper provides also shows the same mechanism of macrophage uptake of alum particles (which CAN be transported across the BBB, effectively reaching the brain - possibly when macrophages are needed to counter brain inflammation) and these particles are less than less than 100 nm (hence nano) source It's essentially that the macrophages become polluted by alum particles, due to lack of enzymes to digest nanoparticles. And exploiting this, macrophages can access the BBB - it's sort of like a Trojan Horse. This mechanism has been explored in other treatments for cancer, especially brain cancer. source And this paper is about biopersistence, which shows alum particles being observed in various organs, even at 270 day mark in rats. 6-in-1 vaccine: Infanrix Hexa (0.82 milligrams) PCV (pneumococcal conjugate vaccine):ar 13 (0.125 milligrams) MenB vaccine: Bexsero (0.5 milligrams) Pre-school Booster vaccines: Repevax (0.33 milligrams), Infanrix IPV (0.5 milligrams) and Boostrix-IPV (0.5 milligrams) HPV vaccine: Gardasil (0.225 milligrams) Teenage Booster vaccine: Revaxis (0.35 milligrams) HepB vaccine: HBVaxPro (0.25 to 0.5 milligrams, depending on which version of HBVaxPro is given) All these vaccines, have aluminum, and many of these are given to infants... IPV, 6-in-1, HepB... and in 1 mole, there are 27g of aluminum - this paper shows that at 10 nanomolar, alum can cause inflammation - which is 27g * (10^-9) * 10 = 270 nano grams, of aluminum. source A typical vaccine contains 250 micrograms (250,000 nano grams), in other words (270/250,000) less than 0.01 % of an alum vaccine can cause inflammation in organs. yet, each vaccine exceeds the "limit" by a factor of almost a thousand times
It's the aluminum suspended in lipid nanoparticles, conjugated with surfactants like polysorbate that greatly open the blood brain barrier, to which the aluminum can biodistribute in lymph after being injected into muscle and then get into the brain. We only just recently discovered the connection between the lymph and nervous system/brain. Our brain detoxification system uses this and it's a 2 way system that distributes immunological factors, neurotransmitters, glutathione and antioxidants, etc. If there are any toxins in the lymph, especially lipid suspended toxins with surfactants, they VERY EASILY get into the brain. This is just objective and I will link the research below substantiating it. source Wanna know how we know vaccines cause autism, primarily through aluminum? Autopsy analysis of the brains of those with autism, as well as alzheimers and MS. They found INORDINATE amounts of Al compared to control. Vaccines are the only vector possible, oral cannot explain such quantities based on all available evidence. source Even with oral exposure, you only absorb 0.01% of it and it rarely goes systemic, nor does it ever go to the brain and deposit into tissue. source source Not only do we have these problems with biodistribution into the brain, we also have severe quality control problems with the vaccines and the amount of Al in the first place, thanks to the complete legal protection pharma has to not give a shit. Demonstrated in these 2 papers. source "However, we present the first robust data obtained using state-of-the-art methods on the aluminium content of vaccines currently being administered in infants. The data are not reassuring. They suggest that vaccine manufacturers have limited control over the aluminium content of their vaccines. The aluminium content of individual vaccines within vaccine lots vary significantly. The amount of aluminium an infant receives in a vaccine is, it would appear, akin to a lottery." source Here is the most damning revelation found. "It should be a matter of concern that a recent freedom of information act request (FOIA Case Number 50882, and HHS Appeal No.;19-0083-AA) revealed that the NIH were unable to provide a single study relied upon by them in relation to the safety of injection of aluminium adjuvants in infants" Here are 2 more papers discussing mechanisms of toxicity and autoimmunity. source source ------------------------------- So in summary, the autopsy brain analysis + quality control concerns + inherent vaccine design with adjuvant conjugations that open blood brain barrier = definitive CAUSAL evidence that vaccines cause autism. We'd know this for absolute sure if the gov/pharma did a double blind placebo RCT with long term health outcomes, but they refuse to do such studies for obvious reasons.
100-1000x more aluminum in vaccines than breast milk in first 6 months of life
"In this context, given their serious conceptual and methodological weaknesses, the 3 available toxico-kinetic studies objectively constitute insufficient bases to guarantee the absolute safety of aluminum adjuvants administered at very large scale, in particular over the long term."