Interferon-β bioactivity measurement in multiple sclerosis: feasibility for routine clinical practice

被引:22
作者
van der Voort, L. F. [1 ]
Kok, A. [2 ]
Visser, A. [2 ]
Oudejans, C. B. M. [2 ]
Caldano, M. [3 ,4 ]
Gilli, F. [3 ,4 ]
Bertolotto, A. [3 ,4 ]
Polman, C. H. [1 ]
Killestein, J. [1 ]
机构
[1] Vrije Univ Amsterdam Med Ctr, Dept Neurol, NL-1007 MB Amsterdam, Netherlands
[2] Vrije Univ Amsterdam Med Ctr, Dept Clin Chem, Amsterdam, Netherlands
[3] ASO S Luigi Gonzaga, Ctr Rifermento Reg Sclerosi Multipla CReSM, Turin, Italy
[4] ASO S Luigi Gonzaga, Neurobiol Clin, Turin, Italy
来源
MULTIPLE SCLEROSIS | 2009年 / 15卷 / 02期
关键词
bioactivity; clinical practice; immune modulating therapy; interferon beta; multiple sclerosis; neutralising antibodies; NEUTRALIZING ANTIBODIES; IFN-BETA; BIOLOGICAL-ACTIVITY; MS PATIENTS; BIOAVAILABILITY; MXA; FREQUENCY; BIOASSAY; EFFICACY; IMPACT;
D O I
10.1177/1352458508096877
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background Neutralising antibodies (NAb) to interferon beta (IFN beta) are associated with a reduced bioactivity and efficacy of IFN beta in multiple sclerosis (MS). Unclear is how to apply IFN beta bioactivity measurements (quantification of Myxovirus resistance protein A (MxA) mRNA) in clinical practice. Objectives To evaluate value and feasibility of IFN beta bioactivity measurement with a single MxA mRNA measurement for screening and a second measurement before and after IFN beta administration for definite confirmation of IFN beta bioactivity status. Methods In 79 MS patients MxA mRNA expression was determined 4 hours after IFN beta administration. If inadequate, MxA mRNA expression testing was repeated 3 months afterwards, comparing post- and pre injection samples to determine whether IFNb bioactivity was persistently lacking. MxA mRNA expression was compared to NA beta titres, determined by the cytopathic effect assay (CPE). Results NAb titres correlated significantly with MxA mRNA expression and MxA mRNA induction. Of all screened patients, only one patient had adequate MxA mRNA expression and high NAb titres simultaneously. Of the biological non-responders at second measurement (21/55), 17 (81%) were high-titre NAb positive, 1 (5%) was low-titre NAb positive and 3 (14%) were NAb negative. Without considering the pre-injection measurement, two more NAb negative patients would have tested negative for IFN beta bioactivity, emphasizing the need of a pre-injection sample. Conclusions Our data suggest that for IFN beta bioactivity screening a single post-injection measurement seems reasonable. However, MxA induction measurement based on both pre- and post-IFN beta injection samples at second measurement is somewhat more precise in determining ultimate IFN beta bioactivity status. Multiple Sclerosis 2009; 15: 212-218. http://msj.sagepub.com
引用
收藏
页码:212 / 218
页数:7
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