Anti-HHV-6 IgG Titer Significantly Predicts Subsequent Relapse Risk in Multiple Sclerosis
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Background: Some of the strongest associations with MS onset are for human herpesviruses, particularly Epstein-Barr virus (EBV) and human herpesvirus 6 (HHV-6). Their role in MS clinical course is less clear, however.
Methods: Prospective cohort of 198 persons with clinically definite MS, followed 2002-5, and serum samples obtained from all subjects at study entry to measure anti-HHV-6 and anti-EBV (Epstein-Barr nuclear antigen [EBNA] and viral capsid antigen [VCA]) IgG titers. Association with relapse evaluated using survival analysis; association with disability/progression evaluated using linear regression or multilevel mixed-effects linear regression.
Results: For the 145 persons with relapsing-remitting MS followed beyond one review, anti-HHV-6 IgG titer was positively associated with the hazard of relapse with a dose-dependent trend (p = 0.003), not affected by adjustment for anti-EBV IgG titers, neither of which were independently associated with relapse. There was no significant association between anti-human herpesvirus IgG titers and baseline-measured disability scores, or change in disability scores; however, anti-HHV-6 IgG titers were 2.8 times higher among progressive-course females than progressive-course males.
Discussion: These findings suggest that, in addition to a potential etiological role in MS, HHV-6 infection or the immune response to HHV-6 antigens may have an effect on the risk of MS relapses and possibly on progressive courses of MS. The observed effect was directly related to anti-HHV-6 IgG titers and may indicate that either HHV-6 infection or factors associated with an altered humoral immune response to HHV-6 may have an effect on MS clinical course. Anti-HHV-6 IgG titer may be a useful prognostic factor in relapsing-remitting MS clinical course.
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Grut V, Bistrom M, Salzer J, Stridh P, Jons D, Gustafsson R Brain. 2023; 147(1):177-185.
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Frau J, Coghe G, Lorefice L, Fenu G, Cocco E Life (Basel). 2023; 13(6).
PMID: 37374092 PMC: 10305018. DOI: 10.3390/life13061309.
Vojdani A, Vojdani E, Saidara E, Maes M Viruses. 2023; 15(2).
PMID: 36851614 PMC: 9967513. DOI: 10.3390/v15020400.
Lezhnyova V, Davidyuk Y, Mullakhmetova A, Markelova M, Zakharov A, Khaiboullina S Front Immunol. 2022; 13:1010605.
PMID: 36451826 PMC: 9703080. DOI: 10.3389/fimmu.2022.1010605.
Pike S, Welsh N, Linzey M, Gilli F Front Mol Neurosci. 2022; 15:1019799.
PMID: 36311024 PMC: 9606571. DOI: 10.3389/fnmol.2022.1019799.