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. 2020 Mar;80(3):320-325.
doi: 10.1016/j.jinf.2019.10.017. Epub 2019 Oct 31.

A different response to cytomegalovirus (CMV) and Epstein-Barr virus (EBV) infection in UK people with multiple sclerosis (PwMS) compared to controls

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A different response to cytomegalovirus (CMV) and Epstein-Barr virus (EBV) infection in UK people with multiple sclerosis (PwMS) compared to controls

Peter A C Maple et al. J Infect. 2020 Mar.

Abstract

Objectives: The nature of past cytomegalovirus (CMV) infection in multiple sclerosis (MS) populations is relatively unexplored. Relationships between CMV infection markers and Epstein-Barr virus (EBV) infection markers in a UK resident population of people with MS (PwMS) and controls have been investigated.

Methods: CMV and EBV nuclear antigen-1(EBNA-1)/virus capsid antigen (VCA) IgG levels were determined for 78 MS patients and anonymised controls by enzyme immunoassays. CMV IgG levels were expressed as Paul Ehrlich Institute (PEI) units/ml (U/ml) and EBNA-1/VCA IgG levels as enzyme units/ml.

Results: CMV IgG seroprevalence was lower (p = 0.0003) in PwMS (35.9% [95%CI: 25.2-46.5]) compared to controls (62.9% [95%CI:54.4-71.4). CMV IgG geometric mean levels in PwMS (353 PEI U/ml [95%CI:272-457]) were lower (p = 0.03) compared to the controls (492 PEI U/ml [95%CI:405-599]). EBNA-1 IgG levels were higher (p < 0.0001) in PwMS compared to the controls and were lower (p = 0.238) in CMV seropositive PwMS (49.4 units/ml [95%CI:32.2-75.6]) compared to CMV seronegative PwMS (65.4 units/ml [95%CI:53.4-80.1]). These effects were not apparent with EBV VCA IgG.

Conclusions: Several aspects of CMV and EBV infection in PwMS appear to differ compared to controls. The potential immunomodulatory effect of CMV infection on MS disease and potential interactions with EBV require further investigation.

Keywords: Cytomegalovirus; Epstein–Barr virus; Multiple sclerosis; Seroprevalence.

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Conflict of interest statement

Declaration of Competing Interest Peter A. C. Maple and Radu Tanasescu have no conflicts of interest. Bruno Gran has received honoraria for consultancy from Merck, Roche, Biogen, and Teva UK and unrestricted research grants from Biogen Idec, Merck, Bayer Healthcare, Teva UK, Novartis, and Genzyme. Cris Constantinescu has provided consultancy for Teva, and MorphoSys and received honoraria/travel grants from Biogen Idec, Novartis, and Teva. He has received also research grants from Biogen Idec, Merck, Serono, Bayer, Schering, MorphoSys, Roche, and Sanofi Pasteur MSD.

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