Sep 18

Reprint

 

The following open letter by a PhD Immunologist completely demolishes the current California legislative initiative to remove all vaccine exemptions. That such a draconian and cynical state statute is under consideration in the ‘Golden State’ is as shocking as it is predictable. After all, it was mysteriously written and submitted shortly after the manufactured-in-Disneyland measles ‘outbreak’.

The indisputable science that is employed by Tetyana Obukhanych, PhD ought to be read by every CA legislator who is entertaining an affirmative vote for SB277. Dr. Obukhanych skillfully deconstructs the many false and fabricated arguments that are advanced by Big Pharma and the U.S Federal Government as they attempt to implement a nationwide Super-Vaccination agenda.


When the California Senate refuses to consider authoritative scientific evidence which categorically proves the dangerous vaccine side effects on the schoolchildren, something is very wrong. Such conduct by the Senate constitutes criminal action that endangers the lives and welfare of children. Their official behavior must be acknowledged for what it is — CRIMINAL — and prosecuted to the fullest extent of the law.

An Open Letter to Legislators Currently Considering Vaccine Legislation from Tetyana Obukhanych, PhD in Immunology

Re: VACCINE LEGISLATION

Dear Legislator:

My name is Tetyana Obukhanych. I hold a PhD in Immunology. I am writing this letter in the hope that it will correct several common misperceptions about vaccines in order to help you formulate a fair and balanced understanding that is supported by accepted vaccine theory and new scientific findings.

Do unvaccinated children pose a higher threat to the public than the vaccinated?

It is often stated that those who choose not to vaccinate their children for reasons of conscience endanger the rest of the public, and this is the rationale behind most of the legislation to end vaccine exemptions currently being considered by federal and state legislators country-wide. You should be aware that the nature of protection afforded by many modern vaccines – and that includes most of the vaccines recommended by the CDC for children – is not consistent with such a statement. I have outlined below the recommended vaccines that cannot prevent transmission of disease either because they are not designed to prevent the transmission of infection (rather, they are intended to prevent disease symptoms), or because they are for non-communicable diseases. People who have not received the vaccines mentioned below pose no higher threat to the general public than those who have, implying that discrimination against non-immunized children in a public school setting may not be warranted.

IPV (inactivated poliovirus vaccine) cannot prevent transmission of poliovirus (see appendix for the scientific study, Item #1). Wild poliovirus has been non-existent in the USA for at least two decades. Even if wild poliovirus were to be re-imported by travel, vaccinating for polio with IPV cannot affect the safety of public spaces. Please note that wild poliovirus eradication is attributed to the use of a different vaccine, OPV or oral poliovirus vaccine. Despite being capable of preventing wild poliovirus transmission, use of OPV was phased out long ago in the USA and replaced with IPV due to safety concerns.

 

Polio Chart

 

Tetanus is not a contagious disease, but rather acquired from deep-puncture wounds contaminated with C. tetani spores. Vaccinating for tetanus (via the DTaP combination vaccine) cannot alter the safety of public spaces; it is intended to render personal protection only.

 

While intended to prevent the disease-causing effects of the diphtheria toxin, the diphtheria toxoid vaccine (also contained in the DTaP vaccine) is not designed to prevent colonization and transmission of C. diphtheriae. Vaccinating for diphtheria cannot alter the safety of public spaces; it is likewise intended for personal protection only.

The acellular pertussis (aP) vaccine (the final element of the DTaP combined vaccine), now in use in the USA, replaced the whole cell pertussis vaccine in the late 1990s, which was followed by an unprecedented resurgence of whooping cough. An experiment with deliberate pertussis infection in primates revealed that the aP vaccine is not capable of preventing colonization and transmission of B. pertussis (see appendix for the scientific study, Item #2). The FDA has issued a warning regarding this crucial finding.[1]

 

Furthermore, the 2013 meeting of the Board of Scientific Counselors at the CDC revealed additional alarming data that pertussis variants (PRN-negative strains) currently circulating in the USA acquired a selective advantage to infect those who are up-to-date for their DTaP boosters (see appendix for the CDC document, Item #3), meaning that people who are up-to-date are more likely to be infected, and thus contagious, than people who are not vaccinated.

 

Among numerous types of H. influenzae, the Hib vaccine covers only type b. Despite its sole intention to reduce symptomatic and asymptomatic (disease-less) Hib carriage, the introduction of the Hib vaccine has inadvertently shifted strain dominance towards other types of H. influenzae (types a through f).These types have been causing invasive disease of high severity and increasing incidence in adults in the era of Hib vaccination of children (see appendix for the scientific study, Item #4). The general population is more vulnerable to the invasive disease now than it was prior to the start of the Hib vaccination campaign. Discriminating against children who are not vaccinated for Hib does not make any scientific sense in the era of non-type b H. influenzae disease.

Hepatitis B is a blood-borne virus. It does not spread in a community setting, especially among children who are unlikely to engage in high-risk behaviors, such as needle sharing or sex. Vaccinating children for hepatitis B cannot significantly alter the safety of public spaces. Further, school admission is not prohibited for children who are chronic hepatitis B carriers. To prohibit school admission for those who are simply unvaccinated – and do not even carry hepatitis B – would constitute unreasonable and illogical discrimination.

 

In summary, a person who is not vaccinated with IPV, DTaP, HepB, and Hib vaccines due to reasons of conscience poses no extra danger to the public than a person who is. No discrimination is warranted.

How often do serious vaccine adverse events happen?

It is often stated that vaccination rarely leads to serious adverse events. Unfortunately, this statement is not supported by science. A recent study done in Ontario, Canada, established that vaccination actually leads to an emergency room visit for 1 in 168 children following their 12-month vaccination appointment and for 1 in 730 children following their 18-month vaccination appointment (see appendix for a scientific study, Item #5).

When the risk of an adverse event requiring an ER visit after well-baby vaccinations is demonstrably so high, vaccination must remain a choice for parents, who may understandably be unwilling to assume this immediate risk in order to protect their children from diseases that are generally considered mild or that their children may never be exposed to.

Can discrimination against families who oppose vaccines for reasons of conscience prevent future disease outbreaks of communicable viral diseases, such as measles?

Measles research scientists have for a long time been aware of the “measles paradox.” I quote from the article by Poland & Jacobson (1994) “Failure to Reach the Goal of Measles Elimination: Apparent Paradox of Measles Infections in Immunized Persons.” Arch Intern Med 154:1815-1820:

“THE APPARENT PARADOX IS THAT AS MEASLES IMMUNIZATION RATES RISE TO HIGH LEVELS IN A POPULATION, MEASLES BECOMES A DISEASE OF IMMUNIZED PERSONS.”[2]

Further research determined that behind the “measles paradox” is a fraction of the population called LOW VACCINE RESPONDERS. Low-responders are those who respond poorly to the first dose of the measles vaccine. These individuals then mount a weak immune response to subsequent RE-vaccination and quickly return to the pool of “susceptibles’’ within 2-5 years, despite being fully vaccinated.[3]

Re-vaccination cannot correct low-responsiveness: it appears to be an immuno-genetic trait.[4] The proportion of low-responders among children was estimated to be 4.7% in the USA.[5]

Studies of measles outbreaks in Quebec, Canada, and China attest that outbreaks of measles still happen, even when vaccination compliance is in the highest bracket (95-97% or even 99%, see appendix for scientific studies, Items #6&7). This is because even in high vaccine responders, vaccine-induced antibodies wane over time. Vaccine immunity does not equal life-long immunity acquired after natural exposure.


It has been documented that vaccinated persons who develop breakthrough measles are contagious. In fact, two major measles outbreaks in 2011 (in Quebec, Canada, and in New York, NY) were re-imported by previously vaccinated individuals.[6] – [7]

Taken together, these data make it apparent that elimination of vaccine exemptions, currently only utilized by a small percentage of families anyway, will neither solve the problem of disease resurgence nor prevent re-importation and outbreaks of previously eliminated diseases.

Is discrimination against conscientious vaccine objectors the only practical solution?

The majority of measles cases in recent US outbreaks (including the recent Disneyland outbreak) are adults and very young babies, whereas in the pre-vaccination era, measles occurred mainly between the ages 1 and 15. Natural exposure to measles was followed by lifelong immunity from re-infection, whereas vaccine immunity wanes over time, leaving adults unprotected by their childhood shots. Measles is more dangerous for infants and for adults than for school-aged children.

Despite high chances of exposure in the pre-vaccination era, measles practically never happened in babies much younger than one year of age due to the robust maternal immunity transfer mechanism. The vulnerability of very young babies to measles today is the direct outcome of the prolonged mass vaccination campaign of the past, during which their mothers, themselves vaccinated in their childhood, were not able to experience measles naturally at a safe school age and establish the lifelong immunity that would also be transferred to their babies and protect them from measles for the first year of life.

Luckily, a therapeutic backup exists to mimic now-eroded maternal immunity. Infants as well as other vulnerable or immunocompromised individuals, are eligible to receive immunoglobulin, a potentially life-saving measure that supplies antibodies directed against the virus to prevent or ameliorate disease upon exposure (see appendix, Item #8).

In summary: 1) due to the properties of modern vaccines, non-vaccinated individuals pose no greater risk of transmission of polio, diphtheria, pertussis, and numerous non-type b H. influenzae strains than vaccinated individuals do, non-vaccinated individuals pose virtually no danger of transmission of hepatitis B in a school setting, and tetanus is not transmissible at all; 2) there is a significantly elevated risk of emergency room visits after childhood vaccination appointments attesting that vaccination is not risk-free; 3) outbreaks of measles cannot be entirely prevented even if we had nearly perfect vaccination compliance; and 4) an effective method of preventing measles and other viral diseases in vaccine-ineligible infants and the immunocompromised, immunoglobulin, is available for those who may be exposed to these diseases.

Taken together, these four facts make it clear that discrimination in a public school setting against children who are not vaccinated for reasons of conscience is completely unwarranted as the vaccine status of conscientious objectors poses no undue public health risk.

Sincerely Yours,

~ Tetyana Obukhanych, PhD

Tetyana Obukhanych, PhD, is the author of the book Vaccine Illusion. She has studied immunology in some of the world’s most prestigious medical institutions. She earned her PhD in Immunology at the Rockefeller University in New York and did postdoctoral training at Harvard Medical School, Boston, MA and Stanford University in California.

Dr. Obukhanych offers online classes for those who want to gain deeper understanding of how the immune system works and whether the immunologic benefits of vaccines are worth the risks: Natural Immunity Fundamentals.

 

 

Appendix

Item #1. The Cuba IPV Study collaborative group. (2007) Randomized controlled trial of inactivated poliovirus vaccine in Cuba. N Engl J Med 356:1536-44

http://www.ncbi.nlm.nih.gov/pubmed/17429085

The table below from the Cuban IPV study documents that 91% of children receiving no IPV (control group B) were colonized with live attenuated poliovirus upon deliberate experimental inoculation. Children who were vaccinated with IPV (groups A and C) were similarly colonized at the rate of 94-97%. High counts of live virus were recovered from the stool of children in all groups. These results make it clear that IPV cannot be relied upon for the control of polioviruses.

polio chart

Item #2. Warfel et al. (2014) Acellular pertussis vaccines protect against disease but fail to prevent infection and transmission in a nonhuman primate model.Proc Natl Acad Sci USA 111:787-92

http://www.ncbi.nlm.nih.gov/pubmed/24277828

“Baboons vaccinated with aP were protected from severe pertussis-associated symptoms but not from colonization, did not clear the infection faster than naïve [unvaccinated] animals, and readily transmitted B. pertussis to unvaccinated contacts. By comparison, previously infected [naturally-immune] animals were not colonized upon secondary infection.”

Item #3. Meeting of the Board of Scientific Counselors, Office of Infectious Diseases, Centers for Disease Control and Prevention, Tom Harkins Global Communication Center, Atlanta, Georgia, December 11-12, 2013

http://www.cdc.gov/maso/facm/pdfs/BSCOID/2013121112_BSCOID_Minutes.pdf

Resurgence of Pertussis (p.6)

“Findings indicated that 85% of the isolates [from six Enhanced Pertussis Surveillance Sites and from epidemics in Washington and Vermont in 2012] were PRN-deficient and vaccinated patients had significantly higher odds than unvaccinated patients of being infected with PRN-deficient strains. Moreover, when patients with up-to-date DTaP vaccinations were compared to unvaccinated patients, the odds of being infected with PRN-deficient strains increased, suggesting that PRN-bacteria may have a selective advantage in infecting DTaP-vaccinated persons.”

Item #4. Rubach et al. (2011) Increasing incidence of invasive Haemophilus influenzae disease in adults, Utah, USA. Emerg Infect Dis 17:1645-50

http://www.ncbi.nlm.nih.gov/pubmed/21888789

The chart below from Rubach et al. shows the number of invasive cases of H. influenzae(all types) in Utah in the decade of childhood vaccination for Hib.

Hib chart

Item #5. Wilson et al. (2011) Adverse events following 12 and 18 month vaccinations: a population-based, self-controlled case series analysis. PLoS One 6:e27897

http://www.ncbi.nlm.nih.gov/pubmed/22174753

“Four to 12 days post 12 month vaccination, children had a 1.33 (1.29-1.38) increased relative incidence of the combined endpoint compared to the control period, or at least one event during the risk interval for every 168 children vaccinated. Ten to 12 days post 18 month vaccination, the relative incidence was 1.25 (95%, 1.17-1.33) which represented at least one excess event for every 730 children vaccinated. The primary reason for increased events was statistically significant elevations in emergency room visits following all vaccinations.”

Item #6. De Serres et al. (2013) Largest measles epidemic in North America in a decade–Quebec, Canada, 2011: contribution of susceptibility, serendipity, and superspreading events. J Infect Dis 207:990-98

http://www.ncbi.nlm.nih.gov/pubmed/23264672

“The largest measles epidemic in North America in the last decade occurred in 2011 in Quebec, Canada.”

“A super-spreading event triggered by 1 importation resulted in sustained transmission and 678 cases.”

“The index case patient was a 30-39-year old adult, after returning to Canada from the Caribbean. The index case patient received measles vaccine in childhood.”

“Provincial [Quebec] vaccine coverage surveys conducted in 2006, 2008, and 2010 consistently showed that by 24 months of age, approximately 96% of children had received 1 dose and approximately 85% had received 2 doses of measles vaccine, increasing to 97% and 90%, respectively, by 28 months of age. With additional first and second doses administered between 28 and 59 months of age, population measles vaccine coverage is even higher by school entry.”

“Among adolescents, 22% [of measles cases] had received 2 vaccine doses. Outbreak investigation showed this proportion to have been an underestimate; active case finding identified 130% more cases among 2-dose recipients.”

Item #7. Wang et al. (2014) Difficulties in eliminating measles and controlling rubella and mumps: a cross-sectional study of a first measles and rubella vaccination and a second measles, mumps, and rubella vaccination. PLoS One9:e89361

http://www.ncbi.nlm.nih.gov/pubmed/24586717

“The reported coverage of the measles-mumps-rubella (MMR) vaccine is greater than 99.0% in Zhejiang province. However, the incidence of measles, mumps, and rubella remains high.”

Item #8. Immunoglobulin Handbook, Health Protection Agency

http://webarchive.nationalarchives.gov.uk/20140714084352/http://www.hpa.org.uk/webc/HPAwebFile/HPAweb_C/1242198450982

HUMAN NORMAL IMMUNOGLOBULIN (HNIG):

Indications

To prevent or attenuate an attack in immuno-compromised contacts

To prevent or attenuate an attack in pregnant women

To prevent or attenuate an attack in infants under the age of 9 months

[1] http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm376937.htm

[2] http://archinte.jamanetwork.com/article.aspx?articleid=619215

[3] Poland (1998) Am J Hum Genet 62:215-220

http://www.ncbi.nlm.nih.gov/pubmed/9463343

“ ‘poor responders,’ who were re-immunized and developed poor or low-level antibody responses only to lose detectable antibody and develop measles on exposure 2–5 years later.”

[4] ibid

“Our ongoing studies suggest that seronegativity after vaccination [for measles] clusters among related family members, that genetic polymorphisms within the HLA [genes] significantly influence antibody levels.”

[5] LeBaron et al. (2007) Arch Pediatr Adolesc Med 161:294-301

http://www.ncbi.nlm.nih.gov/pubmed/17339511

“Titers fell significantly over time [after second MMR] for the study population overall and, by the final collection, 4.7% of children were potentially susceptible.”

[6] De Serres et al. (2013) J Infect Dis 207:990-998

http://www.ncbi.nlm.nih.gov/pubmed/23264672

“The index case patient received measles vaccine in childhood.”

[7] Rosen et al. (2014) Clin Infect Dis 58:1205-1210

http://www.ncbi.nlm.nih.gov/pubmed/24585562

“The index patient had 2 doses of measles-containing vaccine.”

 

Source: Aletho News


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Sep 18

Neuro Immune Connections, MMR Vaccine, Autism and a CDC Whistleblower

Scientists have revealed many neuro-immune connections, a link between the immune system and the brain.

Stunning discovery links the brain and the immune system

This phenomenon is influencing social behavior. The CDC has manipulated studies which are clearly indicating that an MMR vaccine can cause Autism.

CDC Whistleblower Dr William Thomson confesses to MMR vaccine research fraud in historic public statement.
http://www.naturalnews.com/046630_CDC_whistleblower_public_confession_Dr_William_Thompson.html

Quote: https://news.virginia.edu/illimitable/discovery/theyll-have-rewrite-textbooks „It’s a stunning discovery that overturns decades of textbook teaching: researchers at the School of Medicine have determined that the brain is directly connected to the immune system by vessels previously thought not to exist. “I really did not believe there were structures in the body that we were not aware of. I thought the body was mapped,” said Jonathan Kipnis, a professor in the Department of Neuroscience and director of the University’s Center for Brain Immunology and Glia. How these vessels could have escaped detection when the lymphatic system has been so thoroughly mapped throughout the body is surprising on its own.

http://www.nature.com/nature/journal/v535/n7612/full/nature18626.html

But the true significance of the discovery lies in its ramifications for the study and treatment of neurological diseases ranging from autism to Alzheimer’s disease to multiple sclerosis. Kipnis said researchers no longer need to ask questions such as, “How do we study the immune response of the brain?” or “Why do multiple sclerosis patients have immune system attacks?” “Now we can approach this mechanistically — because the brain is like every other tissue connected to the peripheral immune system through meningeal lymphatic vessels,” Kipnis said. “We believe that for every neurological disease that has an immune component to it, these vessels may play a major role.” Kevin Lee, who chairs the Department of Neuroscience, recalled his reaction the first time researchers in Kipnis’ lab shared their basic result with him.“

“I just said one sentence: ‘They’ll have to rewrite the textbooks.’ There has never been a lymphatic system for the central nervous system, and it was very clear from that first singular observation — and they’ve done many studies since then to bolster the finding — that it will fundamentally change the way people look at the central nervous system’s relationship with the immune system,” Lee said.“ Unquote

Quote by University of Virginia (UVA Today): „In a startling discovery that raises fundamental questions about human behavior, researchers at the University of Virginia School of Medicine have determined that the immune system directly affects – and even controls – creatures’ social behavior, such as their desire to interact with others.

https://news.virginia.edu/content/shocking-new-role-found-immune-system-controlling-social-interactions
So could immune system problems contribute to an inability to have normal social interactions? The answer appears to be yes, and that finding could have significant implications for neurological diseases such as autism-spectrum disorders and schizophrenia.

“The brain and the adaptive immune system were thought to be isolated from each other, and any immune activity in the brain was perceived as sign of a pathology. And now, not only are we showing that they are closely interacting, but some of our behavior traits might have evolved because of our immune response to pathogens,” explained Jonathan Kipnis, chair of UVA’s Department of Neuroscience. “It’s crazy, but maybe we are just multicellular battlefields for two ancient forces: pathogens and the immune system. Part of our personality may actually be dictated by the immune system.”
Unquote

Quote by Neuroscience News: „The researchers note that a malfunctioning immune system may be responsible for “social deficits in numerous neurological and psychiatric disorders.” But exactly what this might mean for autism and other specific conditions requires further investigation.

http://neurosciencenews.com/social-behavior-immune-system-4679/
Unquote

Autism can be caused by an immune response and being grasped by a systemic approach called systems biology. Autism is not caused by a mental disorder but by neuro-immune connections

http://www.nature.com/nature/journal/v523/n7560/full/nature14432.html, an area called neuroimmunology. This is closely related to the lymphatic drainage system: Quote (Nature)

http://www.nature.com/nature/journal/v523/n7560/full/nature14432.html : “ Although it is now accepted that the central nervous system undergoes constant immune surveillance that takes place within the meningeal compartment the mechanisms governing the entrance and exit of immune cells from the central nervous system remain poorly understood. In searching for T-cell gateways into and out of the meninges, we discovered functional lymphatic vessels lining the dural sinuses. These structures express all of the molecular hallmarks of lymphatic endothelial cells, are able to carry both fluid and immune cells from the cerebrospinal fluid, and are connected to the deep cervical lymph nodes. The unique location of these vessels may have impeded their discovery to date, thereby contributing to the long-held concept of the absence of lymphatic vasculature in the central nervous system. The discovery of the central nervous system lymphatic system may call for a reassessment of basic assumptions in neuroimmunology and sheds new light on the aetiology of neuroinflammatory and neurodegenerative diseases associated with immune system dysfunction.“ Unquote

This is something that Henry Markram will never figure out by his mathematical models!

Unexpected role of interferon-γ in regulating neuronal connectivity and social behaviour (Nature),
http://www.nature.com/nature/journal/v535/n7612/full/nature18626.html

Quote:
„Immune dysfunction is commonly associated with several neurological and mental disorders. Although the mechanisms by which peripheral immunity may influence neuronal function are largely unknown, recent findings implicate meningeal immunity influencing behaviour, such as spatial learning and memory1. Here we show that meningeal immunity is also critical for social behaviour; mice deficient in adaptive immunity exhibit social deficits and hyper-connectivity of fronto-cortical brain regions. Associations between rodent transcriptomes from brain and cellular transcriptomes in response to T-cell-derived cytokines suggest a strong interaction between social behaviour and interferon-γ (IFN-γ)-driven responses. Concordantly, we demonstrate that inhibitory neurons respond to IFN-γ and increase GABAergic (γ-aminobutyric-acid) currents in projection neurons, suggesting that IFN-γ is a molecular link between meningeal immunity and neural circuits recruited for social behaviour. Meta-analysis of the transcriptomes of a range of organisms reveals that rodents, fish, and flies elevate IFN-γ/JAK-STAT-dependent gene signatures in a social context, suggesting that the IFN-γ signalling pathway could mediate a co-evolutionary link between social/aggregation behaviour and an efficient anti-pathogen response. This study implicates adaptive immune dysfunction, in particular IFN-γ, in disorders characterized by social dysfunction and suggests a co-evolutionary link between social behaviour and an anti-pathogen immune response driven by IFN-γ signalling.“ Unquote

VAXXED, Dr Andrew Wakefield, the Lancet and more fraud by CDC Scientists

In 1998, Dr Andrew Wakefield has published a research paper about „Ileal-lymphoid-nodular hyperplasia, non-specific colitis, and pervasive developmental disorder in children“ http://www.thelancet.com/journals/lancet/article/PIIS0140-6736(97)11096-0/abstract in the Lancet Magazine. This research by Andrew Wakefield has been unjustifiably discredited by many of his colleagues and he was forced to retract the study, accused of fraud and discredited as a scientist.

Despite to all those allegations, Andrew Wakefield, MB.BS, an academic gastroenterologist http://vaxxedthemovie.com/andrew-wakefield-biography/ , moved to Texas in order to prove his claims, a task that he successfully managed. Andrew Wakefield was fully rehabilitated.

 

The cause for Autism is not about the brain but about the bodies problems for detoxification, because there are some poisonous substances in an MMR- Vaccine. Dr Andrew Wakefield has coined some consequences of the toxication in the gut „Autistic Enterocolitis“ and „Inflammatory Bowel  Syndrome“.

 

VAXXED: Dr. Andrew Wakefield Deals With Allegations

Frank DeStefano et al:

Age at first measles-mumps-rubella vaccination in children with autism and school-matched control subjects: a population-based study in metropolitan atlanta.

Quote by John Hewitt on Twitter: There’s 2 Eisens in the progressive academic sphere and they are both total wackjobs. both want our minds controlled by microbiome. https://twitter.com/jhewitt123/status/751026655368536064 M. Eisen, PlosOne editor, has publicly called anyone watching ‚Vaxxed‘ an accessory to murder, that tells you something of his fear. https://twitter.com/jhewitt123/status/751028666088431616

Link between antibiotics in early childhood and autism

Host microbiota constantly control maturation and function of microglia in the CNS
https://www.ncbi.nlm.nih.gov/pubmed/26030851

Host microbiota keep the brain healthy

http://www.bioss.uni-freiburg.de/newsroom-and-media/2015/prinz-microglia-2015/

Quote: „Host microbiota control maturing and functioning of brain immune cells / Short-chain fatty acids function as messengers between the gut and the brain / Publication in Nature Neuroscience

The gut’s microbiome has an impact on the brain’s immune response throughout life, with a possible effect on the course of diseases affecting the brain, such as Alzheimer’s disease or multiple sclerosis. A neuropathological research team at the University Medical Center Freiburg has uncovered these effects in mice. The scientists have been able to demonstrate that the function of microglia, also called brain macrophages, is controlled by metabolites of gut bacteria. During the digestion of fibres, in particular, intestinal bacteria produce short-chain fatty acids necessary for proper microglia function. Mice whose intestines were free of bacteria developed immature and stunted microglia. When intestinal flora was reintroduced, microglia cell morphology and function recovered. This study highlights the importance of a balanced diet for the prevention of brain diseases and indicates that there may be a link between gut bacteria and the genesis of neurodegenerative diseases. These findings will be published in the July issue of the renowned journal Nature Neuroscience and already available as advance online publication.

 

Microglia are also known as phagocytes of the brain, or brain macrophages. They eliminate invading pathogens and dead brain cells, thus contributing to the brain’s life-long plasticity. Malfunctioning microglia cells play a role in a number of brain diseases. Until now, the maturing and activation of these cells has been unclear.“
Unquote

Some Explanations, Quantum Biology, Demise of the Central Dogma of Molecular Biology and Surface Physics

This works by a similar mechanism that works via antibiotics as well, especially when the combined vaccine for measles, mumps and rubella or MMR-Vaccine is applied in early childhood (the stress is on „early“) by an immune response via enteric flora (ENS, Enteric Nervous System) and neurons in conjunction with microorganisms, the lymphatic system, short chain fatty acids and scavenger cells which are influencing the Brain/CNS/Microglia, overcoming the blood cerebral barrier.

The link between an MMR Vaccine and autism is obvious but it is NOT about an anti-vaxxer movement, stop to think in terms of pro vaccination and anti-vaccination. Statistics and studies are misleading about what happens on a global scale.

It is no about an imperative mechanism which is enforcing something, for instance a ‚disease‘, which is a human classification, neglecting the high variability of pathogens. Every human being is a random sample, microorganisms are ‚reproducing‘ themselves in a random process (look up Bet Hedging), it is not a ‚process‘ at all (classic world view) but happens on quantum level.

P-values should not be abused, they are derived by a post Gauß’ian observation (visible light), they are debunked by quantum biology, which says that there is no attribution of cause and effect in the observable world, means that dna cannot be described properly by a static model. There is no direct link between a ‚disease‘ and genetics.

An interpretation of observations by visible light only is misleading about “cause and effect”.

 

These questions are legit: is there any disease in nature? What does it mean when scientists claim to have exterminated a „disease“?

Is there a mismatch between these claims and our observations or our interpretations of our observations?

More appropriate and effective ways in order to protect human beings from a disease are to strengthen their adaptability and their immune system, preparing them for an ongoing change (pathogens) and to research possible causes for health related problems, applying models taking into account multi-causality. Assertions derived by a ‚vaccination coverage rate‘ (by 95% of the targeted population in case of the MMR Vaccine, proposed by the German Robert Koch Institute, RKI) is neglecting this.

In the case of for instance Yersinia pestis, a weakening of the immune system by a small climate shift (no more rain) causing crop failure has prepared the „success“ of this virus within the population of the 14th century in Europe (yersinia pestis exists since the Bronze Age or even longer http://www.cell.com/abstract/S0092-8674(15)01322-7 ). Small pox was not exterminated as well, the same for poliomyelitis: new outbreaks have been reported recently (2016). The polio vaccine is contaminated with SV40, a cancer virus.

Every human being is a random sample, the same for microorganisms, DNA is not determining who we are:

1. p-values are debunked
http://fivethirtyeight.com/features/statisticians-found-one-thing-they-can-agree-on-its-time-to-stop-misusing-p-values/

2. Look up ‚Dark Matter of our genome‘ The demise of the Central Dogma of Molecular Biology.
http://sandwalk.blogspot.de/2007/01/central-dogma-of-molecular-biology.html

3. Spatial alignment and quantum properties reveal the mistakes made by Crick and Watson:
The interpretation of DNA as a static model with base pairs and a double-helix structure is not taking into account the ‚Dark Matter‘ of our genome. Crick and Watson were even not able to figure out an appropriate interpretation of the double helix structure (guess who has done this? http://www.biography.com/people/rosalind-franklin-9301344), DNA is just a basic pattern which permanently transforms and is being transformed by, for instance, epigenetics, proteomics, junk-dna, RNA viruses, virome, trans-splicing, transposons, prions, gene rearrangements and so forth, but the more appropriate model is a quantum state model that is not interfering in a 3D world but within topological layers and a permanent phase transition, indicated by quantum markers, in view to permanent changes, by, for instance, surface physics (for instance docking mechanism for T-Cells or Antibodies), epigenetics or protein membrane foldings. These are metastatical states on quantum level.

 

Quantum Markers are about a phase transition, for instance, the transition of IgA to IgM.

Please remind that there are no “perfect” quantum states as such as “start” or “finishing” point as such in nature, for the instance, there is no representation of the “ 1” or 0 (Zero) in nature as such but the (space) topological (transition, phase transition) n-fractal “measuring up” of existence via non existence and vice versa. There are no spatial rotations within a “3D” space, as Carl Friedrich Gauß has shown. Look up “Inner Infinity Notion of Existence in n-fractal dimensional transitions at horizons” and “ A phase Crystal for the economic phase transition”.

Further reading and sources:

Topical gentamicin-induced hearing loss: a mitochondrial ribosomal RNA study of genetic susceptibility.
https://www.ncbi.nlm.nih.gov/pubmed/8915412

VAXXED Documentary Explored with Filmmakers on Antidote

Andy Wakefield on the History and Causation of Autism

John Hewitt on Twitter: „discovery was very well hyped, definitely many neuro-immune connections“

Impfungen verursachen Autismus – der Betrug der CDC – gefälschte Studien

https://www.youtube.com/watch?v=0OgLDexr4Io&t=0s

Link between the immune system and the brain – neuro-immune connections

http://hixgrid.de/blog/view/49410/link-between-the-immune-system-and-the-brain-neuro-immune-connections

 

 

WATCH DOCUMENTARY MOVIE -An Autism Media Channel Film
Directed by Andrew Wakefield & Produced by Del Bigtree

“Our children are being destroyed by vaccines,” says Del Bigtree
In 2013, biologist Dr. Brian Hooker received a call from a Senior Scientist at the U.S. Centers for Disease Control and Prevention (CDC) who led the agency’s 2004 study on the Measles-Mumps-Rubella (MMR) vaccine and its link to autism.
The scientist, Dr. William Thompson, confessed that the CDC had omitted crucial data in their final report that revealed a causal relationship between the MMR vaccine and autism. Over several months, Dr. Hooker records the phone calls made to him by Dr. Thompson who provides the confidential data destroyed by his colleagues at the CDC.

Dr. Hooker enlists the help of Dr. Andrew Wakefield, the British gastroenterologist falsely accused of starting the anti-vax movement when he first reported in 1998 that the MMR vaccine may cause autism. In his ongoing effort to advocate for children’s health, Wakefield directs this documentary examining the evidence behind an appalling cover-up committed by the government agency charged with protecting the health of American citizens.
Interviews with pharmaceutical insiders, doctors, politicians, and parents of vaccine-injured children reveal an alarming deception that has contributed to the skyrocketing increase of autism and potentially the most catastrophic epidemic of our lifetime.

 

 

Google Short URL  goo.gl/ttlwkj

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