Intravenous immunoglobulins containing antibodies against β-amyloid for the treatment of Alzheimer's disease

被引:264
作者
Dodel, RC
Du, Y
Depboylu, C
Hampel, H
Frölich, L
Haag, A
Hemmeter, U
Paulsen, S
Teipel, SJ
Brettschneider, S
Spottke, A
Nölker, C
Möller, HJ
Wei, X
Farlow, M
Sommer, N
Oertel, WH
机构
[1] Univ Bonn, Dept Neurol, D-53105 Bonn, Germany
[2] Indiana Univ, Dept Neurol, Indianapolis, IN 46204 USA
[3] Univ Munich, Dept Psychiat, D-8000 Munich, Germany
[4] Univ Frankfurt, Dept Psychiat, Frankfurt, Germany
[5] Univ Marburg, Dept Neurol, D-35032 Marburg, Germany
[6] Univ Marburg, Dept Psychiat, D-35032 Marburg, Germany
关键词
D O I
10.1136/jnnp.2003.033399
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Active or passive immunisation can mitigate plaque pathology in murine models of Alzheimer's disease (AD). Recently, it has been shown that antibodies against β-amyloid (Aβ) are present in human immunoglobulin preparations (IVIgG), which specifically recognise and inhibit the neurotoxic effects of Aβ. This study reports the results from a pilot study using IVIgG in patients with AD. Methods: Five patients with AD were enrolled and received monthly IVIgG over a 6 month period. Efficacy assessment included total Aβ/Aβ1-42 measured in the CSF/serum as well as effects on cognition (ADAS-cog; CERAD) at baseline and at 6 months following IVIgG. Results: Following IVIgG, total Aβ levels in the CSF decreased by 30.1% (17.3-43.5%) compared to baseline (p<0.05). Total Aβ increased in the serum by 233% (p<0.05). No significant change was found in Aβ1-42 levels in the CSF/serum. Using ADAS-cog, an improvement of 3.7±2.9 points was detected. Scores in the MMSE were essentially unchanged (improved in four patients, stable in one patient) following IVIgG compared to baseline. Conclusion: Although the sample size of this pilot study is too small to draw a clear conclusion, the results of this pilot study provide evidence for a more detailed investigation of IVIgG for the treatment of AD.
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页码:1472 / 1474
页数:3
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