Mitochondrial Destruction in Autistic Children a Present in Early Childhood From Vaccine Makers
Abstract Autism spectrum disorder (ASD) consists of a group of complex developmental disabilities characterized by impaired social interactions, deficits in communication and repetitive behavior. Multiple lines of evidence implicate mitochondrial dysfunction in ASD. In postmortem BA21 temporal cortex, a region that exhibits synaptic pathology in ASD, we found that compared to controls, ASD patients exhibited altered protein levels of mitochondria respiratory chain protein complexes, decreased Complex I and IV activities, decreased mitochondrial antioxidant enzyme SOD2, and greater oxidative DNA damage. Mitochondrial membrane mass was higher in ASD brain, as indicated by higher protein levels of mitochondrial membrane proteins Tom20, Tim23 and porin. No differences were observed in either mitochondrial DNA or levels of the mitochondrial gene transcription factor TFAM or cofactor PGC1α, indicating that a mechanism other than alterations in mitochondrial genome or mitochondrial biogenesis underlies these mitochondrial abnormalities. We further identified higher levels of the mitochondrial fission proteins (Fis1 and Drp1) and decreased levels of the fusion proteins (Mfn1, Mfn2 and Opa1) in ASD patients, indicating altered mitochondrial dynamics in ASD brain. Many of these changes were evident in cortical pyramidal neurons, and were observed in ASD children but were less pronounced or absent in adult patients. Together, these findings provide evidence that mitochondrial function and intracellular redox status are compromised in pyramidal neurons in ASD brain and that mitochondrial dysfunction occurs during early childhood when ASD symptoms appear.
Highlights
► We identify mitochondria respiratory chain protein defects and oxidative stress in autism brain temporal lobe. ► We found altered mitochondrial dynamics in autism temporal lobe. ► We report the neuronal accumulation of compromised mitochondria in temporal lobe of autism brain. ► We detected no mtDNA mutations in ASD brain. ► Mechanisms regulating mitochondrial gene transcription are intact in autism brain temporal lobe.
► We identify mitochondria respiratory chain protein defects and oxidative stress in autism brain temporal lobe. ► We found altered mitochondrial dynamics in autism temporal lobe. ► We report the neuronal accumulation of compromised mitochondria in temporal lobe of autism brain. ► We detected no mtDNA mutations in ASD brain. ► Mechanisms regulating mitochondrial gene transcription are intact in autism brain temporal lobe.
http://www.sciencedirect.com/science/article/pii/S0969996113000302
What is the root cause of Autism Spectrum Disorder?
Vaccines are the root cause of Autism (until recently occurring at a rate of 1 in 67…then 1 in 60, now spiking exponentially to as high as 1 in 38 in some regions– ‘individuals born in 2003 have 16.6 times the odds of an autism diagnosis compared with those born in 1992.‘). Officially, the rate of Autism amongst children has risen to as high as 1 in 50, based on the glaring testimony of 100,000 parents in the US. By 2015, the statistics will conservatively match that of 1 in 38.
This is primarily due to accumulative damage from the Hepatitis B (Hep B), Pneumococcal conjugate vaccine (PCV), Haemophilus-B influenza (HIB),Inactivated Polio (IPV), Influenza (seasonal), Diphtheria, Tetanus, Pertussis (DTaP) & Measles, Mumps, Rubella (MMR) shots (an accumulation of multiple live viruses, excipient + heavy metal build-up)…
– leading to Ischemia, a singing/clogging of the delicate neural pathways from toxic overload which prevents vital oxygen from reaching the brain, literally inhibiting normal development, triggering what are termed “microvascular strokes” (‘as large white blood cells rush to attack the foreign particles injected into our bloodstream…surround tiny capillaries where the foreign particles land, clog and collapse the capillaries.’).
Anaphylaxis, a system-wide allergic & functional breakdown, described as ‘a severe, whole-body allergic reaction to a chemical that has become an allergen‘, and Encephalitis, inflammation of the brain & meninges (Meningoencephalitis) manifesting as ‘diffuse and/or focal neuropsychological dysfunction‘, inevitably follow.
‘Ischemia is known to lead to hyperexcitability of neural tissue.’ Charles A. Lantz, Ph.D. on the impact of Ischemia & resulting vertebral subluxation (misalignment of spinal bones) on neural function
“Almost any vaccination can lead to noninfectious inflammatory reaction involving the nervous system. The common denominator consists of vasculopathy (disease of the blood vessels) that is often associated with demyelination (permeation of the critical “electrical” insulator of the brain cells).” Charles M. Poser, Harvard Medical School Department of Neurology, 1947..
https://www.youtube.com/watch?feature=player_embedded&v=3Gqfr7GTB7w
“Vaccination to Conserved Influenza Antigens in Mice Using a Novel Simian Adenovirus Vector, PanAd3, Derived from the Bonobo Pan paniscus”
PLoS ONE 8(3): e55435. doi:10.1371/journal.pone.0055435
"scientists made their vaccine by genetically modifying a virus called PanAd3, which was isolated from a bonobo (a type of great ape). The modified virus, called a vector,"
FDA approves first GMO Flu Vaccine containing Reprogrammed Insect Virus
A new vaccine for influenza has hit the market, and it is the first ever to contain genetically-modified (GM) proteins derived from insect cells. According to reports, the U.S. Food and Drug Administration (FDA) recently approved the vaccine, known as Flublok, which contains recombinant DNA technology and an insect virus known as baculovirus that is purported to help facilitate the more rapid production of vaccines.
According to Flublok’s package insert, the vaccine is trivalent, which means it contains GM proteins from three different flu strains. The vaccine’s manufacturer, Protein Sciences Corporation (PSC), explains that Flublok is produced by extracting cells from the fall armyworm, a type of caterpillar, and genetically altering them to produce large amounts of hemagglutinin, a flu virus protein that enables the flu virus itself to enter the body quickly.
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