Myalgic encephalomyelitis/chronic fatigue syndrome and gulf war illness patients exhibit increased humoral responses to the herpesviruses‐encoded dUTPase: Implications in disease pathophysiology

Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Gulf War Illness (GWI) are debilitating diseases with overlapping symptomology and there are currently no validated tests for definitive diagnosis of either syndrome. While there is evidence supporting the premise that some herpesviruse...

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Veröffentlicht in:Journal of medical virology 2017-09, Vol.89 (9), p.1636-1645
Hauptverfasser: Halpin, Peter, Williams, Marshall Vance, Klimas, Nancy G., Fletcher, Mary Ann, Barnes, Zachary, Ariza, Maria Eugenia
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container_issue 9
container_start_page 1636
container_title Journal of medical virology
container_volume 89
creator Halpin, Peter
Williams, Marshall Vance
Klimas, Nancy G.
Fletcher, Mary Ann
Barnes, Zachary
Ariza, Maria Eugenia
description Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Gulf War Illness (GWI) are debilitating diseases with overlapping symptomology and there are currently no validated tests for definitive diagnosis of either syndrome. While there is evidence supporting the premise that some herpesviruses may act as possible triggers of ME/CFS, the involvement of herpesviruses in the pathophysiology of GWI has not been studied in spite of a higher prevalence of ME/CFS in these patients. We have previously demonstrated that the deoxyuridine triphosphate nucleotidohydrolases (dUTPase) encoded by Epstein‐Barr virus (EBV), human herpesvirus‐6 (HHV‐6), and varicella‐zoster virus (VZV) possess novel functions in innate and adaptive immunity. The results of this study demonstrate that a significant percentage of patients with ME/CFS (30.91‐52.7%) and GWI (29.34%) are simultaneously producing antibodies against multiple human herpesviruses‐encoded dUTPases and/or the human dUTPase when compared to controls (17.21%). GWI patients exhibited significantly higher levels of antibodies to the HHV‐6 and human dUTPases than controls (P = 0.0053 and P = 0.0036, respectively), while the ME/CFS cohort had higher anti‐EBV‐dUTPase antibodies than in both GWI patients (P = 0.0008) and controls (P 
doi_str_mv 10.1002/jmv.24810
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While there is evidence supporting the premise that some herpesviruses may act as possible triggers of ME/CFS, the involvement of herpesviruses in the pathophysiology of GWI has not been studied in spite of a higher prevalence of ME/CFS in these patients. We have previously demonstrated that the deoxyuridine triphosphate nucleotidohydrolases (dUTPase) encoded by Epstein‐Barr virus (EBV), human herpesvirus‐6 (HHV‐6), and varicella‐zoster virus (VZV) possess novel functions in innate and adaptive immunity. The results of this study demonstrate that a significant percentage of patients with ME/CFS (30.91‐52.7%) and GWI (29.34%) are simultaneously producing antibodies against multiple human herpesviruses‐encoded dUTPases and/or the human dUTPase when compared to controls (17.21%). GWI patients exhibited significantly higher levels of antibodies to the HHV‐6 and human dUTPases than controls (P = 0.0053 and P = 0.0036, respectively), while the ME/CFS cohort had higher anti‐EBV‐dUTPase antibodies than in both GWI patients (P = 0.0008) and controls (P &lt; 0.0001) as well as significantly higher anti‐human dUTPase antibodies than in controls (P = 0.0241). 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GWI patients exhibited significantly higher levels of antibodies to the HHV‐6 and human dUTPases than controls (P = 0.0053 and P = 0.0036, respectively), while the ME/CFS cohort had higher anti‐EBV‐dUTPase antibodies than in both GWI patients (P = 0.0008) and controls (P &lt; 0.0001) as well as significantly higher anti‐human dUTPase antibodies than in controls (P = 0.0241). 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GWI patients exhibited significantly higher levels of antibodies to the HHV‐6 and human dUTPases than controls (P = 0.0053 and P = 0.0036, respectively), while the ME/CFS cohort had higher anti‐EBV‐dUTPase antibodies than in both GWI patients (P = 0.0008) and controls (P &lt; 0.0001) as well as significantly higher anti‐human dUTPase antibodies than in controls (P = 0.0241). These results suggest that screening of patients’ sera for the presence of various combinations of anti‐dUTPase antibodies could be used as potential biomarkers to help identify/distinguish patients with these syndromes and better direct treatment.</abstract><cop>United States</cop><pmid>28303641</pmid><doi>10.1002/jmv.24810</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-2560-5367</orcidid><oa>free_for_read</oa></addata></record>
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source Wiley-Blackwell Journals; MEDLINE
subjects Adult
antibodies
Antibodies, Viral - blood
Autoantibodies - blood
chronic fatigue syndrome
Cohort Studies
deoxyuridine triphosphate nucleotidohydrolase
Diagnosis, Differential
Epstein‐Barr virus
Fatigue Syndrome, Chronic - diagnosis
Fatigue Syndrome, Chronic - immunology
Female
Herpesvirus 4, Human - enzymology
Herpesvirus 4, Human - immunology
Herpesvirus 6, Human - enzymology
Herpesvirus 6, Human - immunology
human herpesvirus 6
Humans
Male
Middle Aged
Persian Gulf Syndrome - diagnosis
Persian Gulf Syndrome - immunology
Pyrophosphatases - immunology
varicella‐zoster virus
title Myalgic encephalomyelitis/chronic fatigue syndrome and gulf war illness patients exhibit increased humoral responses to the herpesviruses‐encoded dUTPase: Implications in disease pathophysiology
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