Is it time to call Chronic Fatigue Syndrome HHV-6/CFS?

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Human Herpesvirus-6 Reactivation, Mitochondrial Fragmentation, and the Coordination of Antiviral and Metabolic Phenotypes in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome




Philipp Schreiner, Thomas Harrer, Carmen Scheibenbogen, Stephanie Lamer, Andreas Schlosser, Robert K. Naviaux and Bhupesh K. Prusty


ImmunoHorizons April 1, 2020, 4 (4) 201-215; DOI: https://doi.org/10.4049/immunohorizons.2000006

Abstract

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a multifactorial disorder with many possible triggers. Human herpesvirus (HHV)–6 and HHV-7 are two infectious triggers for which evidence has been growing. To understand possible causative role of HHV-6 in ME/CFS, metabolic and antiviral phenotypes of U2-OS cells were studied with and without chromosomally integrated HHV-6 and with or without virus reactivation using the histone deacetylase inhibitor trichostatin-A. Proteomic analysis was conducted by pulsed stable isotope labeling by amino acids in cell culture analysis. Antiviral properties that were induced by HHV-6 transactivation were studied in virus-naive A549 cells challenged by infection with influenza-A (H1N1) or HSV-1. Mitochondria were fragmented and 1-carbon metabolism, dUTPase, and thymidylate synthase were strongly induced by HHV-6 reactivation, whereas superoxide dismutase 2 and proteins required for mitochondrial oxidation of fatty acid, amino acid, and glucose metabolism, including pyruvate dehydrogenase, were strongly inhibited. Adoptive transfer of U2-OS cell supernatants after reactivation of HHV-6A led to an antiviral state in A549 cells that prevented superinfection with influenza-A and HSV-1. Adoptive transfer of serum from 10 patients with ME/CFS produced a similar fragmentation of mitochondria and the associated antiviral state in the A549 cell assay. In conclusion, HHV-6 reactivation in ME/CFS patients activates a multisystem, proinflammatory, cell danger response that protects against certain RNA and DNA virus infections but comes at the cost of mitochondrial fragmentation and severely compromised energy metabolism.

https://www.immunohorizons.org/content/4/4/201

From 1988-1997, a newspaper called New York Native warned the world about HHV-6. The AIDS activists and HIV establishment tried to silence them, but they continued to publish uncompromising information about HHV-6 and Chronic Fatigue Syndrome that the CDC, Fauci, and NIH didn't want the public to know about. Now read the whole story about New York Native and the cover-up of HHV-6 epidemic that includes AIDS, Chronic Fatigue Syndrome, Multiple Sclerosis, autism, and many other immunological illnesses.

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New cartoon

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From a forthcoming Julian Lake collection of cartoons about P-hacking in AIDS and Chronic Fatigue Syndrome research. Don't know what P-hacking is? Read this article in the New York Times . Julian Lake most recent collection of cartoons about Chronic Fatigue Syndrome and AIDS is here . See more of Julian Lake's P-hacking cartoon at P-hack University . To learn more about the P-hacking culture of AIDS, Chronic Fatigue Syndrome, and public health science at the CDC and NIH, read Truth to Power , or Iatrogenocide , or if you really have a sense of humor and like wicked satire, Pig: A Memoir .
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  The case for rethinking AIDS based on autopsies like those by George Hensley centers on findings that Kaposi's Sarcoma (KS)—long considered an opportunistic disease secondary to immunodeficiency—may in fact be an essential and primary feature of the AIDS disease process itself, rather than merely a side consequence. ​ Autopsy Evidence: KS as Core to AIDS Studies led by George Hensley demonstrated KS-like lesions in approximately 95% of AIDS autopsies, far higher than the clinical diagnosis rate for KS in living AIDS patients. ​ Inflammatory and morphologic variants of KS were found almost universally in the bodies of those who died with AIDS, across all known risk groups—not just the well-recognized visible lesions but also internal ones. ​ These findings suggest KS is not rare nor merely opportunistic in the context of AIDS, but rather a fundamental tissue pathology, casting doubt on the belief that KS is a secondary event following profound immunosuppression. ​ HHV-8 Weakness a...
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Oral Kaposi's Sarcoma looks like the Crimson Crescents in Chronic Fatigue Syndrome patients.

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This is what oral Kaposi's Sarcoma looks like. Source:  https://doctorspiller.com/kaposis-sarcoma/ Compare it to these crimson crescent lesions in the mouths of Chronic Fatigue Syndrome patients. "Burke A. Cunha, MD, discovered what he called crimson crescents in the mouths of 80% of his CFS patients. After the word got out, Cunha received calls from other parts of the country. Physicians began telling him that they also were finding the crimson crescents in their patients once they looked for them." https://www.prohealth.com/library/crimson-crescents-facilitate-chronic-fatigue-syndrome-cfs-diagnosis-11266 Chronic Fatigue Syndrome patients may have undiagnosed internal Kaposi's Sarcoma. Susan Levin found HHV-8, the Kaposi's Sarcoma virus, in half of CFS patients she looked at. Prevalence in the Cerebrospinal Fluid of the Following Infectious Agents in a Cohort of 12 CFS Subjects Susan Levine Published online: 04 Dec 2011 ABSTR...
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