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Journal ArticleDOI

Lateral flow immunoassay with upconverting nanoparticle‐based detection for indirect measurement of interferon response by the level of MxA

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TLDR
A lateral flow immunoassay (LFIA) with upconverting nanoparticle (UCNP) reporters was developed and evaluated with clinical whole blood samples to assess the potential for a rapid and user‐friendly quantitative assay for MxA, since the currently available rapid test for MXA (FebriDX) produces only qualitative result.
Abstract
Myxovirus resistance protein A (MxA) is a biomarker of interferon-induced gene expression state involved in many viral infections and some autoimmune disorders. It has a variety of potential utilities in clinical diagnostics, including distinguishing between bacterial and viral infections. Currently, MxA-assays are used for monitoring of IFN-β therapy in multiple sclerosis (MS) patients. As a proof-of-concept for rapid quantitative measurement of interferon response, a lateral flow immunoassay (LFIA) with upconverting nanoparticle (UCNP) reporters was developed and evaluated with clinical whole blood samples to assess the potential for a rapid and user-friendly quantitative assay for MxA, since the currently available rapid test for MxA (FebriDX) produces only qualitative result. The high detection sensitivity enabled by the UCNP reporter technology allowed the sample pre-treatment with dilution of whole blood into lysis buffer at a detectable analyte concentration. The assay can be done within 2 hr and the results correlate with the reference MxA-ELISA, which requires an overnight incubation. With 36 samples, R2 for linear regression was 0.86. The assay detected 96% of the IFN-β responders with 89% specificity using a cut-off level of 100 μg/L for an elevated MxA-concentration. J. Med. Virol. 89:598-605, 2017. © 2016 Wiley Periodicals, Inc.

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References
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Journal ArticleDOI

Upconversion and Anti-Stokes Processes with f and d Ions in Solids

TL;DR: Before the 1960s, all anti-Stokes emissions, which were known to exist, involved emission energies in excess of excitation energies by only a few kT and were linked to thermal population of energy states above excitation states by such an energy amount.
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Human MxA protein: an interferon-induced dynamin-like GTPase with broad antiviral activity.

TL;DR: The structural and functional data suggest that MxA targets the nucleoprotein of M xA-sensitive viruses, and may form oligomeric rings around tubular nucleocapsid structures, thereby inhibiting their transcriptional and replicative function.
Journal ArticleDOI

Upconverting phosphor reporters in immunochromatographic assays.

TL;DR: UCP lateral flow assays can be used for applications that are currently limited by assay sensitivity, and they can increase the probability of a diagnosis by verifying the presence of several analytes in the same sample.
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Type I interferon-inducible gene expression in blood is present and reflects disease activity in dermatomyositis and polymyositis.

TL;DR: Most patients with active DM or PM, but not patients with IBM, had significant and high up-regulation of the type I interferon-alpha/beta (IFNalpha/ beta)-inducible genes in blood, which correlated with disease activity in DM and PM.
Journal ArticleDOI

Induction of MxA Gene Expression by Influenza A Virus Requires Type I or Type III Interferon Signaling

TL;DR: MxA is a unique marker for the detection of type I and type III IFN activity during virus infections and IFN therapy, and cannot be triggered directly by virus infection.
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