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Will the Zika Virus Open the Door to Studies on Stealth Adapted Viruses?


February 14, 2016 - 5:00 PM


SOUTH PASADENA, CA - The world is quickly realizing the enormous devastation that virus infections can cause on the developing brain of children prior to birth. Unfortunately, this realization is coming years after the public health authorities disregard of a grouping of viruses, which fail to evoke an inflammatory response; the accepted hallmark of an infectious process. The immune system normally targets only a few of the different components that comprise each virus type. Deletion or mutation of these relatively few, normally targeted antigens can lead to derivative viruses that are not recognized by the cellular immune system. These viruses are termed stealth and the immune evasion mechanism called stealth adaptation.


The early reluctance of public health authorities to acknowledge the existence of stealth adapted viruses was due, in part, to the unequivocal finding that some of these viruses arose from cytomegaloviruses of monkeys used to produce polio vaccine. Moreover, cytomegalovirus contamination of polio vaccines tested in Africa best explains the origin of HIV.

Microcephaly in infants born to Zika virus infected mothers is presently largely confined to Brazil. This may reflect a genetic change in the Brazilian Zika virus. It is also consistent with a facilitating role of co-infection with a stealth adapted virus. Cytomegalovirus can infect the placenta and can promote the replication of other viruses in normally on-permissive cells. Certainly, the affected infants should be examined for stealth adapted virus infections. This can most readily be accomplished using virus cultures. Animals and certain insects can also be susceptible to stealth adapted viruses.

Possibly relevant to the Brazilian outbreak is that routine vaccination can provoke the severity of stealth adapted virus infections. This is relevant in view of the Brazilian government to earlier decision to administer tetanus, diphtheria and acellular pertussis vaccine (Tdap) to all pregnant women.

Once public health authorities engage in these studies, they will come to realize that stealth adapted virus infection is the underlying cause of many neuropsychiatric illnesses, including autism in children. This finding will have major ramifications with regards to the safety of vaccines.

The more promising aspect of studies on stealth adapted viruses is the identification of a non-immunological virus defense mechanism mediated by the alternative cellular energy (ACE) pathway. This pathway has been shown to be effective against herpes viruses, papillomaviruses and HIV. It is likely effective against flaviviruses, including the Zika virus. The ACE pathway is mediated by a dynamic (kinetic) energy of the body's fluids. It results from the absorption of a natural environmental force termed KELEA (kinetic energy limiting electrostatic attraction). Water can be activated by the addition of KELEA attracting compounds, which can subsequently be removed by filtration or repeated dilutions, as in homeopathy. Water can also be activated by being placed in the vicinity of KELEA attracting energy fields. Consuming KELEA activated water provides a convenient way of activating the ACE pathway. Even while waiting for the results of controlled clinical, animal and laboratory testing, urgent consideration should be given to providing KELEA activated water to pregnant women in Zika endemic areas.

A research article addressing this issue has appeared in the Journal of Human Virology and Retrovirology and is available at http://medcraveonline.com/JHVRV/JHVRV-03-00080.pdf
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