Polyspecific, antiviral immune response distinguishes multiple sclerosis and neuromyelitis optica

被引:66
作者
Jarius, S. [2 ,3 ,4 ]
Franciotta, D. [5 ]
Bergamaschi, R. [5 ]
Rauer, S. [6 ]
Wandinger, K. P. [7 ]
Petereit, H. F. [8 ]
Maurer, M. [9 ]
Tumani, H. [10 ]
Vincent, A. [3 ,4 ]
Eichhorn, P. [11 ]
Wildemann, B. [12 ]
Wick, M. [11 ]
Voltz, R. [1 ,2 ]
机构
[1] Univ Cologne, Dept Palliat Med, D-50924 Cologne, Germany
[2] Univ Munich, Inst Clin Neuroimmunol, Munich, Germany
[3] Univ Oxford, John Radcliffe Hosp, Neurosci Grp, Weatherall Inst Mol Med, Oxford OX3 9DU, England
[4] Univ Oxford, John Radcliffe Hosp, Dept Neurol, Oxford OX3 9DU, England
[5] Univ Pavia, Neurol Inst C Mondino, IRCCS Fdn, I-27100 Pavia, Italy
[6] Univ Freiburg, Dept Neurol, D-7800 Freiburg, Germany
[7] Charite Univ Med Berlin, Dept Neurol, Berlin, Germany
[8] Univ Cologne, Dept Neurol, D-50924 Cologne, Germany
[9] Univ Wurzburg, Dept Neurol, D-8700 Wurzburg, Germany
[10] Univ Ulm, Dept Neurol, D-7900 Ulm, Germany
[11] Univ Munich, Dept Clin Chem, Munich, Germany
[12] Univ Heidelberg, Dept Neurol, Div Mol Neuroimmunol, Heidelberg, Germany
关键词
D O I
10.1136/jnnp.2007.133330
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: A polyspecific, intrathecal humoral immune response against neurotropic viruses such as measles, rubella and varicella zoster virus (MRZ reaction, MRZR) is present in 80-100% of patients with multiple sclerosis (MS), but has not to date been evaluated in patients with neuromyelitis optica (NMO). Aims: To evaluate whether MRZR distinguishes NMO and MS. Methods: 20 patients with NMO and 42 with MS were included. The intrathecal synthesis of antibodies against measles, rubella and varicella zoster virus was detected by calculation of the respective antibody indices (AI). Results: A positive MRZ reaction, as defined by a combination of at least two positive AIs, was found in 37/42 MS, but in only 1/20 NMO patients (p < 0.0001). Median AI values differed significantly between the groups (p < 0.0005). Conclusions: The polyspecific antiviral humoral immune response characteristic for MS is widely missing in NMO, irrespective of the NMO-IgG status of the patients. Our findings further strengthen the case for NMO being pathologically distinct from MS.
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收藏
页码:1134 / 1136
页数:3
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