Activation of Transposable Elements in Immune Cells of Fibromyalgia Patients.
Tamara Ovejero, Océane Sadones, Teresa Sánchez-Fito, Eloy Almenar-Pérez, José Andrés Espejo, Eva Martín-Martínez, Lubov Nathanson, Elisa Oltra
Author Information
Tamara Ovejero: School of Medicine, Universidad Católica de Valencia San Vicente Mártir, 46001 Valencia, Spain.
Océane Sadones: Université de Poitiers, CEDEX, 86073 Poitiers, France. ORCID
Teresa Sánchez-Fito: Escuela de Doctorado, Universidad Católica de Valencia San Vicente Mártir, 46008 Valencia, Spain. ORCID
Eloy Almenar-Pérez: Escuela de Doctorado, Universidad Católica de Valencia San Vicente Mártir, 46008 Valencia, Spain.
José Andrés Espejo: School of Biotechnology, Universidad Católica de Valencia San Vicente Mártir, 46001 Valencia, Spain.
Eva Martín-Martínez: National Health Service, Manises Hospital, 46940 Valencia, Spain.
Lubov Nathanson: Institute for Neuro Immune Medicine, Nova Southeastern University, Ft Lauderdale, FL 33314, USA. ORCID
Elisa Oltra: School of Medicine, Universidad Católica de Valencia San Vicente Mártir, 46001 Valencia, Spain. ORCID
中文译文
English
Advancements in nucleic acid sequencing technology combined with an unprecedented availability of metadata have revealed that 45% of the human genome constituted by transposable elements (TEs) is not only transcriptionally active but also physiologically necessary. Dysregulation of TEs, including human retroviral endogenous sequences (HERVs) has been shown to associate with several neurologic and autoimmune diseases, including Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS). However, no study has yet addressed whether abnormal expression of these sequences correlates with fibromyalgia (FM), a disease frequently comorbid with ME/CFS. The work presented here shows, for the first time, that, in fact, HERVs of the H, K and W types are overexpressed in immune cells of FM patients with or without comorbid ME/CFS. Patients with increased HERV expression (N = 14) presented increased levels of interferon (INF-β and INF-γ) but unchanged levels of TNF-α. The findings reported in this study could explain the flu-like symptoms FM patients present with in clinical practice, in the absence of concomitant infections. Future work aimed at identifying specific genomic loci differentially affected in FM and/or ME/CFS is warranted.
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2018-121-001/Universidad Católica de Valencia San Vicente Mártir
Adult
Aged
Cytokines
DNA Transposable Elements
Endogenous Retroviruses
Fatigue
Female
Fibromyalgia
Humans
Leukocytes
Linear Models
Male
Middle Aged
Models, Biological
RNA, Transfer
Surveys and Questionnaires
Cytokines
DNA Transposable Elements
RNA, Transfer