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Influenza and acellular pertussis vaccines not only fail to protect, they increase susceptibility and severity of disease upon infection – benefits are overrated and the risks are being ignored

Arumugham, Vinu

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        <foaf:name>Arumugham, Vinu</foaf:name>
    <dct:title>Influenza and acellular pertussis vaccines not only fail to protect, they increase susceptibility and severity of disease upon infection – benefits are overrated and the risks are being ignored</dct:title>
    <dct:issued rdf:datatype="">2019</dct:issued>
    <dcat:keyword>mucosal immunity</dcat:keyword>
    <dcat:keyword>cell mediated immunity</dcat:keyword>
    <dcat:keyword>linked epitope suppression</dcat:keyword>
    <dcat:keyword>aluminum adjuvant</dcat:keyword>
    <dcat:keyword>multiple sclerosis</dcat:keyword>
    <dct:issued rdf:datatype="">2019-01-05</dct:issued>
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    <dct:description>&lt;p&gt;The influenza vaccine fails often. The influenza vaccines cause the development of IgE mediated&lt;br&gt; allergy to the influenza virus. The reason for failure include antigenic mismatch between vaccine strain&lt;br&gt; and wild virus, IgE mediated antigen neutralization, etc. Naturally acquired immunity against influenza&lt;br&gt; lasts for decades. Vaccine based immunity lasts for a few months. Replacing natural immunity with&lt;br&gt; vaccine-based immunity, progressively increases susceptibility over time. In 2016-18, between 46 and&lt;br&gt; 68% of patients admitted to the ICU for severe influenza were vaccinated with the influenza vaccine, in&lt;br&gt; California. The influenza vaccine uptake in the general population in California during that same period&lt;br&gt; was between 40-48%. This adds to evidence that not only does the influenza vaccine fail, it can&lt;br&gt; contribute to increased disease severity. The increase in disease severity is due to patients suffering an&lt;br&gt; allergic reaction against the virus, concurrent with the influenza infection.&lt;br&gt; The acellular pertussis vaccine (APV) fails to protect for more than a year in most patients, fails to&lt;br&gt; provide mucosal immunity, fails to provide cell mediated immunity and fails to protect against airway&lt;br&gt; colonization with Bordetella pertussis (BP) bacteria. Therefore the APV causes asymptomatic&lt;br&gt; spreading of BP. The exact opposite effect of herd immunity - herd spreading. The APV causes IgE&lt;br&gt; mediated sensitization directed against BP antigens. Therefore once colonized, continuing exposure to&lt;br&gt; BP antigens results in asthma. Colonization with BP can cause multiple sclerosis. The APV contains&lt;br&gt; cow&amp;rsquo;s milk proteins used to manufacture the vaccine. The milk proteins include bovine casein, bovine&lt;br&gt; insulin and bovine folate receptor proteins. The result is the development of milk allergy, type 1&lt;br&gt; diabetes and autism respectively. Colonization can induce immune tolerance to BP, making an infection&lt;br&gt; even more dangerous and rendering the patient potentially unprotectable for life with a future pertussis&lt;br&gt; vaccine.&lt;/p&gt; &lt;p&gt;&amp;nbsp;&lt;/p&gt;</dct:description>
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