Epstein-Barr Virus Load Correlates with Multiple Sclerosis-Associated Retrovirus Envelope Expression.
Silvia Perez-PerezMaría Inmaculada Domínguez-MozoMaría Ángel García-MartínezRubén Ballester-GonzálezIsrael GañánRafael ArroyoRoberto Álvarez-LafuentePublished in: Biomedicines (2022)
pHERV-W ENV and syncytin-1, the envelope proteins of the human endogenous retrovirus W family (HERV-W), have been proposed as etiological factors for MS development. In addition, herpesviruses, such as the Epstein-Barr virus (EBV) and the human herpesvirus 6A/B (HHV-6A/B), have been also strongly associated with the disease. This work aims to study the possible link between viral loads and antibody titers against EBV and HHV-6A/B and the pHERV-W ENV/syncytin-1 protein/gene expression. For this purpose, we conducted a 12-month longitudinal study involving 98 RRMS patients. Peripheral blood samples were obtained from each patient. Serum antibody titers against EBV and HHV-6A/B were determined by ELISA, while viral loads were analyzed using qPCR. HLA MS-related alleles were also genotyped. pHERV-W ENV/syncytin-1 protein and gene expression levels in immune cells were assessed by flow cytometry and qPCR, respectively. We found that the 12-month variation of the pHERV-W ENV gene expression levels positively correlated with the variation of the EBV viral load, especially in those patients with high baseline EBV loads. Therefore, these results could support previous studies pointing to the transactivation of pHERV-W ENV by EBV. However, further studies are needed to better understand this possible relationship.
Keyphrases
- epstein barr virus
- gene expression
- multiple sclerosis
- diffuse large b cell lymphoma
- dna methylation
- endothelial cells
- flow cytometry
- peripheral blood
- end stage renal disease
- mass spectrometry
- sars cov
- newly diagnosed
- chronic kidney disease
- induced pluripotent stem cells
- ms ms
- peritoneal dialysis
- pluripotent stem cells
- prognostic factors
- case control
- amino acid
- white matter
- long non coding rna