United States set
language
Menu Shopping cart $0 Search
Distributed product

Bi-VirTest for Human MxA POCT

  • Regulatory status:RUO
  • Type:Lateral Flow Test
  • Other names:Myxovirus resistance protein 1, MX1, Myxovirus-Resistant Protein A, Interferon-regulated resistance GTP-binding protein MxA, Interferon-Inducible Protein p78
  • Species:Human
Cat. No. Size Price


New BI005-10 10 tests / package
PubMed Product Details
Technical Data

Don't miss related products

Bi-Reader

Discover more in product brochures:

Human MxA POCT
MxA in managing infections and immune responses

Type

Lateral Flow Test

Description

Diferentiation between viral and bacterial infections
Viral infections: acute phase disease monitoring

Quantitative Measuring Range

5-200 ng/ml

Cut-off

21 ng/ml

Clinical Sensitivity and Specificity

≥ 93% and 95%

Assay Time

15 minutes

Applications

Capillary Blood

Summary

Features

  • European Union: for in vitro diagnostic use
  • Rest of the world: for research use only!

Research topic

Immune Response, Infection and Inflammation, Sepsis, COVID-19

Summary

Human MxA protein (Myxovirus resistance protein 1), encoded by the MX1 gene, is a 76-kDa protein composed of 662 amino acid residues and is a member of the dynamin superfamily of large GTPases. The MxA protein plays a crucial role in antiviral defense within cells, providing protection against a broad range of viruses, including influenza, parainfluenza, measles, coxsackie, hepatitis B, and Thogoto viruses.

The viruses are inhibited by MxA protein at an early stage in their life cycle, soon after host cell entry and before genome amplification. The human MxA protein is accumulated in the cytoplasm and endoplasmic reticulum. The membrane compartment of endoplasmatic reticulum seems to provide an interaction platform that facilitates viral target recognition. MxA appears to detect viral infection by sensing and trapping nucleocapsid structures, and becoming the viral components unavailable for the generation of new virus particles.The expression of viral MxA protein is induced exclusively and, in a dose-dependent manner, by IFN-alpha and IFN-beta, but not by IFN-gamma, IL-1, TNF-alpha or other cytokines.

MxA protein may offer advantages as a laboratory marker because of its very low basal concentration, increasing within 1-2 hours of infection and long half-life being approximately 2-3 days. In mononuclear cells stimulated with high doses of leukocyte IFN-alpha, MxA mRNA levels increased tenfold within 4 hours, and elevated MxA protein levels persists over the next 48 hours. MxA protein with its low basal concentration and long half-life, offers advantages as a marker for viral infection. Clinical studies have reported on MxA protein in peripheral blood mononuclear cells as a marker distinguishing viral from bacterial disease, and as a reliable marker for type I IFN bioavailability during IFN treatment in patients with multiple sclerosis (MS) according to the recommendation from EMA (European Medicine Agency).

Main Clinical Use of MxA

  • Differentiating viral from bacterial infections
  • Detection and assessment of active phase of Viral Infections
  • Immune response assessment
  • Autoimmune and inflammatory disease activity marker
  • Therapeutic monitoring in interferon therapy
Summary References (10)

References to MxA Protein

  • Bachur RG, Harper MB. Predictive model for serious bacterial infections among infants younger than 3 months of age. Pediatrics. 2001 Aug;108 (2):311-6
  • Chieux V, Hober D, Harvey J, Lion G, Lucidarme D, Forzy G, Duhamel M, Cousin J, Ducoulombier H, Wattre P. The MxA protein levels in whole blood lysates of patients with various viral infections. J Virol Methods. 1998 Feb;70 (2):183-91
  • Haller O, Kochs G. IFN-induced mx proteins: dynamin-like GTPases with antiviral activity. Traffic. 2002 Oct;3 (10):710-7
  • Haller O, Staeheli P, Kochs G. IFN-induced Mx proteins in antiviral host defense. Biochimie. 2007 Jun-Jul;89 (6-7):812-8
  • Halminen M, Ilonen J, Julkunen I, Ruuskanen O, Simell O, Makela MJ. Expression of MxA protein in blood lymphocytes discriminates between viral and bacterial infections in febrile children. Pediatr Res. 1997 May;41 (5):647-50
  • Huppertz HI, Becker K, Kreth HW. Clinical value of measuring the IFN-induced enzyme 2'-5'-oligoadenylate synthetase in children. Acta Paediatr. 1992 Apr;81 (4):329-34
  • Koskenvuo MM, Halminen M, Blomqvist M, Vainionpaa R, Ilonen J, Julkunen I, Salmi TT, Makela MJ. Expression of MxA protein in blood lymphocytes of children receiving anticancer chemotherapy. Pediatr Hematol Oncol. 2006 Dec;23 (8):649-60
  • Nakabayashi M, Adachi Y, Itazawa T, Okabe Y, Kanegane H, Kawamura M, Tomita A, Miyawaki T. MxA-based recognition of viral illness in febrile children by a whole blood assay. Pediatr Res. 2006 Dec;60 (6):770-4
  • Simon A, Fah J, Haller O, Staeheli P. IFN-regulated Mx genes are not responsive to interleukin-1, tumor necrosis factor, and other cytokines. J Virol. 1991 Feb;65 (2):968-71
  • Vallittu AM, Eralinna JP, Ilonen J, Salmi AA, Waris M. MxA protein assay for optimal monitoring of IFN-beta bioactivity in the treatment of MS patients. Acta Neurol Scand. 2008 Jul;118 (1):12-7
Related Products Docs
Subscribe to Our Newsletter! Discover News from
BioVendor R&D
Subscribe Now
Subscribe to Our Newsletter! Discover News from
BioVendor R&D
Subscribe Now
zavřít