Epstein-Barr Virus and Multiple Sclerosis

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Standard

Epstein-Barr Virus and Multiple Sclerosis. / Houen, Gunnar; Trier, Nicole Hartwig; Frederiksen, Jette Lautrup.

I: Frontiers in Immunology, Bind 11, 587078, 2020.

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Harvard

Houen, G, Trier, NH & Frederiksen, JL 2020, 'Epstein-Barr Virus and Multiple Sclerosis', Frontiers in Immunology, bind 11, 587078. https://doi.org/10.3389/fimmu.2020.587078

APA

Houen, G., Trier, N. H., & Frederiksen, J. L. (2020). Epstein-Barr Virus and Multiple Sclerosis. Frontiers in Immunology, 11, [587078]. https://doi.org/10.3389/fimmu.2020.587078

Vancouver

Houen G, Trier NH, Frederiksen JL. Epstein-Barr Virus and Multiple Sclerosis. Frontiers in Immunology. 2020;11. 587078. https://doi.org/10.3389/fimmu.2020.587078

Author

Houen, Gunnar ; Trier, Nicole Hartwig ; Frederiksen, Jette Lautrup. / Epstein-Barr Virus and Multiple Sclerosis. I: Frontiers in Immunology. 2020 ; Bind 11.

Bibtex

@article{8d12c944356c45a9bc486ca3e6ef0035,
title = "Epstein-Barr Virus and Multiple Sclerosis",
abstract = "Multiple sclerosis (MS) is a neurologic disease affecting myelinated nerves in the central nervous system (CNS). The disease often debuts as a clinically isolated syndrome, e.g., optic neuritis (ON), which later develops into relapsing-remitting (RR) MS, with temporal attacks or primary progressive (PP) MS. Characteristic features of MS are inflammatory foci in the CNS and intrathecal synthesis of immunoglobulins (Igs), measured as an IgG index, oligoclonal bands (OCBs), or specific antibody indexes. Major predisposing factors for MS are certain tissue types (e.g., HLA DRB1*15:01), vitamin D deficiency, smoking, obesity, and infection with Epstein-Barr virus (EBV). Many of the clinical signs of MS described above can be explained by chronic/recurrent EBV infection and current models of EBV involvement suggest that RRMS may be caused by repeated entry of EBV-transformed B cells to the CNS in connection with attacks, while PPMS may be caused by more chronic activity of EBV-transformed B cells in the CNS. In line with the model of EBV{\textquoteright}s role in MS, new treatments based on monoclonal antibodies (MAbs) targeting B cells have shown good efficacy in clinical trials both for RRMS and PPMS, while MAbs inhibiting B cell mobilization and entry to the CNS have shown efficacy in RRMS. Thus, these agents, which are now first line therapy in many patients, may be hypothesized to function by counteracting a chronic EBV infection.",
keywords = "central nervous system, chronic infection, Epstein-Barr virus, immune evasion, multiple sclerosis, relapsing-remitting",
author = "Gunnar Houen and Trier, {Nicole Hartwig} and Frederiksen, {Jette Lautrup}",
year = "2020",
doi = "10.3389/fimmu.2020.587078",
language = "English",
volume = "11",
journal = "Frontiers in Immunology",
issn = "1664-3224",
publisher = "Frontiers Research Foundation",

}

RIS

TY - JOUR

T1 - Epstein-Barr Virus and Multiple Sclerosis

AU - Houen, Gunnar

AU - Trier, Nicole Hartwig

AU - Frederiksen, Jette Lautrup

PY - 2020

Y1 - 2020

N2 - Multiple sclerosis (MS) is a neurologic disease affecting myelinated nerves in the central nervous system (CNS). The disease often debuts as a clinically isolated syndrome, e.g., optic neuritis (ON), which later develops into relapsing-remitting (RR) MS, with temporal attacks or primary progressive (PP) MS. Characteristic features of MS are inflammatory foci in the CNS and intrathecal synthesis of immunoglobulins (Igs), measured as an IgG index, oligoclonal bands (OCBs), or specific antibody indexes. Major predisposing factors for MS are certain tissue types (e.g., HLA DRB1*15:01), vitamin D deficiency, smoking, obesity, and infection with Epstein-Barr virus (EBV). Many of the clinical signs of MS described above can be explained by chronic/recurrent EBV infection and current models of EBV involvement suggest that RRMS may be caused by repeated entry of EBV-transformed B cells to the CNS in connection with attacks, while PPMS may be caused by more chronic activity of EBV-transformed B cells in the CNS. In line with the model of EBV’s role in MS, new treatments based on monoclonal antibodies (MAbs) targeting B cells have shown good efficacy in clinical trials both for RRMS and PPMS, while MAbs inhibiting B cell mobilization and entry to the CNS have shown efficacy in RRMS. Thus, these agents, which are now first line therapy in many patients, may be hypothesized to function by counteracting a chronic EBV infection.

AB - Multiple sclerosis (MS) is a neurologic disease affecting myelinated nerves in the central nervous system (CNS). The disease often debuts as a clinically isolated syndrome, e.g., optic neuritis (ON), which later develops into relapsing-remitting (RR) MS, with temporal attacks or primary progressive (PP) MS. Characteristic features of MS are inflammatory foci in the CNS and intrathecal synthesis of immunoglobulins (Igs), measured as an IgG index, oligoclonal bands (OCBs), or specific antibody indexes. Major predisposing factors for MS are certain tissue types (e.g., HLA DRB1*15:01), vitamin D deficiency, smoking, obesity, and infection with Epstein-Barr virus (EBV). Many of the clinical signs of MS described above can be explained by chronic/recurrent EBV infection and current models of EBV involvement suggest that RRMS may be caused by repeated entry of EBV-transformed B cells to the CNS in connection with attacks, while PPMS may be caused by more chronic activity of EBV-transformed B cells in the CNS. In line with the model of EBV’s role in MS, new treatments based on monoclonal antibodies (MAbs) targeting B cells have shown good efficacy in clinical trials both for RRMS and PPMS, while MAbs inhibiting B cell mobilization and entry to the CNS have shown efficacy in RRMS. Thus, these agents, which are now first line therapy in many patients, may be hypothesized to function by counteracting a chronic EBV infection.

KW - central nervous system

KW - chronic infection

KW - Epstein-Barr virus

KW - immune evasion

KW - multiple sclerosis

KW - relapsing-remitting

U2 - 10.3389/fimmu.2020.587078

DO - 10.3389/fimmu.2020.587078

M3 - Review

C2 - 33391262

AN - SCOPUS:85098671902

VL - 11

JO - Frontiers in Immunology

JF - Frontiers in Immunology

SN - 1664-3224

M1 - 587078

ER -

ID: 255105401