Honarmand Hamidreza, Ahmadi Jalali Moghadam Masoumeh, Hatamian Hamidreza, Roudbary Ali
Department of Microbiology, Faculty of Medicine, Guilan University of Medical Sciences, Rasht, IR Iran.
Cellular and Molecular Research Center, Faculty of Medicine, Guilan University of Medical Sciences, Rasht, IR Iran.
Jundishapur J Microbiol. 2015 Jun 27;8(6):e15985. doi: 10.5812/jjm.15985v2. eCollection 2015 Jun.
Multiple sclerosis (MS) is a demyelinating condition affecting the central nervous system. Although the cause of this condition is unknown, patients with MS seem to have genetic vulnerability to certain environmental factors such as infection that could trigger this condition.
We conducted this study to determine whether MS risk increases following primary infection with Epstein-Barr virus (EBV) and also to investigate any association between MS and seropositivity to anti-EBNA-1 IgG, anti-EBV-CA IgG, and anti-EBV-EA.
EBV infection was confirmed using the Enzyme-Linked Immunoassay in the patient (n = 46) and control (n = 46) groups via commercial assays (anti-EBNA-1 IgG, anti-EBV-CA IgG, and anti-EBV-EA kits). The data were analyzed by using three statistical tests (Pearson chi-square, Spearman rho correlation, and odds ratio).
Seropositivity to anti-EBNA-1 IgG did not show a significant difference between the patient and control groups (92.9% and 88.4%, respectively), and nor was seropositivity to anti-EBV-CA IgG different between the two groups (95.2% and 95.3%, consequently). The anti-EBV-EA-D test was negative in all the patients and in 95.3% of the controls. Seropositivity to both anti-EBNA-1 and anti-EBV-CA indicating past infection did not show significant associations with the later development of MS (Pearson chi-square asymptotic significance [Asymp. Sig.] [2-sided] = 0.317, Spearman's rho correlation test Sig. [2-sided] = 0.689, odds ratio = 1.95).
Seropositivity to both EBNA1- IgG and EBV-CA- IgG did not show a causal association with MS. The findings of this study suggest that EBV past infection could not be a causative factor in the development of MS and a protective factor against classic MS.
多发性硬化症(MS)是一种影响中枢神经系统的脱髓鞘疾病。尽管这种疾病的病因尚不清楚,但MS患者似乎对某些环境因素(如感染)具有遗传易感性,而这些因素可能引发该疾病。
我们开展这项研究以确定初次感染爱泼斯坦-巴尔病毒(EBV)后MS风险是否增加,并调查MS与抗EBNA-1 IgG、抗EBV-CA IgG和抗EBV-EA血清阳性之间的任何关联。
通过商业检测试剂盒(抗EBNA-1 IgG、抗EBV-CA IgG和抗EBV-EA试剂盒),使用酶联免疫吸附测定法在患者组(n = 46)和对照组(n = 46)中确认EBV感染。数据通过三种统计检验(Pearson卡方检验、Spearman秩相关检验和比值比)进行分析。
患者组和对照组之间抗EBNA-1 IgG的血清阳性率无显著差异(分别为92.9%和88.4%),两组之间抗EBV-CA IgG的血清阳性率也无差异(分别为95.2%和95.3%)。所有患者和95.3%的对照组中抗EBV-EA-D检测均为阴性。抗EBNA-1和抗EBV-CA血清阳性表明既往感染,与MS的后期发生无显著关联(Pearson卡方检验渐近显著性[渐近显著性][双侧]=0.317,Spearman秩相关检验显著性[双侧]=0.689,比值比=1.95)。
EBNA1-IgG和EBV-CA-IgG的血清阳性与MS无因果关联。本研究结果表明,既往EBV感染不是MS发生的致病因素,也不是经典MS的保护因素。