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Frequent HHV-6 reactivation in multiple sclerosis (MS) and chronic fatigue syndrome (CFS) patients
D V Ablashi1, H B Eastman, C B Owen
1Department of Microbiology, Georgetown University, School of Medicine, Washington, DC, USA. dablashi@abionline.com
Background:
HHV-6 is a ubiquitous virus and its infection usually occurs in childhood and then becomes a latent infection. HHV-6 reactivation has been shown to play a role in the pathogenesis of AIDS and several other diseases.
Objectives:
To determine what role HHV-6 infection or reactivation plays in the pathogenesis of multiple sclerosis (MS) and chronic fatigue syndrome (CFS).
Results:
Twenty-one MS and 35 CFS patients were studied and followed clinically. In these patients, we measured HHV-6 IgG and IgM antibody levels and also analyzed their peripheral blood mononuclear cells (PBMCs) for the presence of HHV-6, using a short term culture assay. In both MS and CFS patients, we found higher levels of HHV-6 IgM antibody and elevated levels of IgG antibody when compared to healthy controls. Seventy percent of the MS patients studied contained IgM antibodies for HHV-6 late antigens (capsid), while only 15% of the healthy donors (HD) and 20% of the patients with other neurological disorders (OND) had HHV-6 IgM antibodies. Higher frequency of IgM antibody was also detected in CFS patients (57.1%) compared to HD (16%). Moreover, 54% of CFS patients exhibited antibody to HHV-6 early protein (p41/38) compared to only 8.0% of the HD. Elevated IgG antibody titers were detected in both the MS and the CFS patients. PBMCs from MS, CFS and HD were analyzed in a short term culture assay in order to detect HHV-6 antigen expressing cells and to characterize the viral isolates obtained as either Variant A or B. Fifty-four percent of MS patients contained HHV-6 early and late antigen producing cells and 87% of HHV-6 isolates were Variant B. Isolates from CFS, patients were predominately Variant A (70%) and isolates from HD were predominately Variant B (67%). Moreover, one isolate from OND was also Variant B. Persistent HHV-6 infection was found in two CFS patients over a period of 2.5 years and HHV-6 specific cellular immune responses were detected in PBMCs from ten CFS patients.
Conclusion:
In both MS and CFS patients, we found increased levels of HHV-6 antibody and HHV-6 DNA. A decrease in cellular immune responses was also detected in CFS patients. These data suggest that HHV-6 reactivation plays a role in the pathogenesis of these disorders.
Insights
Human herpesvirus 6 (HHV-6) reactivation may contribute to multiple sclerosis (MS) and chronic fatigue syndrome (CFS). Studies show elevated HHV-6 antibodies and DNA in MS and CFS patients, suggesting a role in disease development.
Area of Science:
- Virology
- Immunology
- Neurology
Background:
- Human herpesvirus 6 (HHV-6) is a common virus causing latent infections.
- HHV-6 reactivation is implicated in the pathogenesis of AIDS and other diseases.
Purpose of the Study:
- To investigate the role of HHV-6 infection and reactivation in the pathogenesis of multiple sclerosis (MS).
- To determine the role of HHV-6 infection and reactivation in the pathogenesis of chronic fatigue syndrome (CFS).
Main Methods:
- Measured HHV-6 IgG and IgM antibody levels in MS and CFS patients compared to healthy donors.
- Analyzed peripheral blood mononuclear cells (PBMCs) for HHV-6 presence using short-term culture assays.
- Characterized HHV-6 isolates as Variant A or B.
Main Results:
- MS and CFS patients exhibited higher HHV-6 IgM and IgG antibody levels than healthy controls.
- HHV-6 DNA was detected in PBMCs of MS and CFS patients, with specific variants predominant in each group.
- Persistent HHV-6 infection and altered cellular immune responses were observed in CFS patients.
Conclusions:
- Elevated HHV-6 antibodies and DNA in MS and CFS patients suggest a role in disease pathogenesis.
- Decreased cellular immune responses in CFS patients may be linked to HHV-6 reactivation.
- Further research is warranted to elucidate the precise mechanisms of HHV-6 involvement in MS and CFS.