Key result
Neutralising antibody titres correlated significantly with MxA mRNA expression, with 81% (17/21) of biological non-responders testing positive for high-titre antibodies.
Why the study?
Does MxA mRNA expression measurement accurately determine interferon beta bioactivity status compared to neutralising antibody titres in patients with multiple sclerosis?
Observational (n=79)
Does MxA mRNA expression measurement accurately determine interferon beta bioactivity status compared to neutralising antibody titres in patients with multiple sclerosis?
A single post-injection MxA mRNA measurement is feasible for screening interferon beta bioactivity in MS patients, though paired pre- and post-injection samples offer greater precision for confirmation.
MxA mRNA may indicate interferon bioactivity in MS; leaves open its adoption for guiding therapy without prospective trials.
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.
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Voort et al. (2008) conducted an observational in multiple sclerosis (n=79). MxA mRNA expression measurement vs. Neutralising antibodies (NAb) titres was evaluated on Correlation between NAb titres and MxA mRNA expression/induction. Neutralising antibody titres correlated significantly with MxA mRNA expression, with 81% (17/21) of biological non-responders testing positive for high-titre antibodies.
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