CLIA CMV

Chemiluminescence kit for the detection of IgG, IgA or IgM antibodies to Cytomegalovirus
in human serum or plasma

Human cytomegalovirus (CMV, Human Herpesvirus 5, HHV 5) is a member of the Herpetoviridae family. In humans, it is mainly transmitted by the respiratory apparatus or urogenital tract. The disease is usually asymptomatic or mild, the latent infection can be reactivated in pregnancy, serious disease, stress, or immunosuppressive treatment. An individuum can be reinfected by a different CMV strain. CMV infection during pregnancy causes developmental defects. The virus is easily transmitted through the placenta during primary infection (in 30-50 % of cases); during the reactivation stage, transplacental transmission occurs in only 1% of cases. CMV infection belongs to the TORCH syndrome.

Serological methods are used for the detection of specific IgA, IgM, and IgG (avidity) antibodies to CMV in laboratory diagnosis of the infection.

Antibodies of IgA class are a sign of an active infection – primary infection as well as reactivation. Production of IgM antibodies usually increases a few weeks after infection or reactivation and then decreases slowly. IgM determination alone cannot discriminate primary infection from reactivation. Specific IgG seroconversion indicates primary infection. The method of IgG avidity detection is used for discrimination between primary infection and reactivation. It is important for the risk assessment of congenital transmission.

Products

100 Tests
Article no.: 71048 Request
100 Tests
Article no.: 71046 Request
100 Tests
Article no.: 71047 Request

Advantages

  • Detection of IgG, IgA or IgM antibodies to Human Cytomegalovirus (CMV)
  • Detection of CMV infection
  • Screening blood donors for CMV infection
  • Disease staging
  • Intended for human serum, citrate plasma
  • Purified and inactivated antigen isolated from CMV AD 169 strain with a high content of specific immunodominant epitopes used
  • The kits are CE-IVD certified and intended for professional use 
  • For each CLIA kit a corresponding control set is available
Assay stability 30 days in-board-stability / in-use-stability until the expiration date at storage temperature 2-8 °C
Sample matrix Serum, Plasma
Measuring range 0.1 - 160 U/ml (IgG), 2 - 160 U/ml (IgA), 0.5 - 160 U/ml (IgM)
Assay/kit content Reagent Cartridge with specific reagents for the assay, magnetic particles, calibrators