Antibodies to Human Herpesviruses in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Patients

Jonas Blomberg1, Muhammad Rizwan1, Agnes Böhlin-Wiener1

  • 1Section of Clinical Microbiology, Department of Medical Sciences, Uppsala University, Uppsala, Sweden.

Frontiers in Immunology
|September 3, 2019
PubMed

Insights

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) patients showed similar overall IgG antibody levels to herpesviruses as healthy controls. However, subtle differences in reactivity suggest a distinct immune response to certain herpesviruses in ME/CFS.

Area of Science:

  • Immunology
  • Virology
  • Neurology

Background:

  • Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a complex, debilitating illness often triggered by infection.
  • Human herpesviruses (HHV), including Epstein-Barr virus (EBV), have been investigated for their potential role in ME/CFS pathogenesis.

Purpose of the Study:

  • To investigate serological evidence of past infections and reactivations of human herpesviruses (HHV-1-7) in ME/CFS patients.
  • To compare immunoglobulin G (IgG) antibody reactivities to various herpesviral antigens between ME/CFS patients and healthy controls.

Main Methods:

  • Utilized a suspension multiplex immunoassay (SMIA) to measure IgG antibodies against whole viruses, recombinant proteins, and synthetic peptides of HHV-1-7.
  • Analyzed samples from ME/CFS patients diagnosed using Canada criteria and healthy Swedish blood donors.

Main Results:

  • Overall IgG antibody reactivity to HHV-1-7 antigens did not significantly differ between ME/CFS patients and controls.
  • Minor, yet notable, relative differences in antibody reactivity were observed for specific antigens, including whole virus HHV-1 and recombinant EBV antigens (EBNA6, EA).

Conclusions:

  • ME/CFS patients exhibit largely comparable IgG antibody levels to common herpesviruses as healthy individuals.
  • Subtle serological distinctions in immune responses to certain herpesviral antigens in ME/CFS patients may indicate unique interactions between their immune systems and these ubiquitous viruses.

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