An enzyme linked immunoassay using recombinant antigens for differentiation of primary from secondary or past CMV infections in pregnancy

J Clin Virol. 1998 Aug 20;11(2):93-102. doi: 10.1016/s1386-6532(98)00052-x.

Abstract

Background: As primary cytomegalovirus (CMV) infection in pregnancy may be associated with severe fetal outcome, the serological differentiation of primary infection from recurrent or previous infection is of major importance.

Objectives: This differentiation was attempted with a CMV IgG enzyme immunoassay (EIA), which investigated the differential IgG immune response to recombinant proteins p52 and pp150. To express the IgG reactivity to either protein a ratio was calculated by OD p52/OD pp150.

Study design: Serial samples from groups of pregnant women with primary infection (n = 18) were compared to those with recurrent (n = 7) or previous CMV infection (n = 189).

Results: In primary infected women a predominant IgG response to p52 (p52 alone or ratio > or = 1.5) was observed in early sera less than 4 weeks after seroconversion, whereas the IgG response to recombinant protein pp150 was delayed and appeared after 2-7 weeks. Women with secondary and those with past infection had either IgG antibodies to pp150 alone or a ratio of less than 1.5 in 85 and 89.1% respectively with no remarkable change of ratio over time.

Conclusions: The IgG recombinant EIA was shown to be a useful supplementary assay for differentiation of primary up to 8 weeks after seroconversion from recurrent or past infections.

MeSH terms

  • Antibodies, Viral / blood
  • Antigens, Viral / immunology*
  • Cytomegalovirus Infections / immunology*
  • Cytomegalovirus Infections / virology
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / immunology
  • Female
  • Humans
  • Immunoenzyme Techniques / methods*
  • Immunoglobulin G / blood
  • Pregnancy
  • Pregnancy Complications, Infectious / immunology*
  • Pregnancy Complications, Infectious / virology
  • Pregnancy Outcome
  • Recombinant Proteins / immunology*
  • Recurrence
  • Sensitivity and Specificity
  • Viral Proteins / genetics
  • Viral Proteins / immunology

Substances

  • Antibodies, Viral
  • Antigens, Viral
  • DNA-Binding Proteins
  • ICP36 protein, Cytomegalovirus
  • Immunoglobulin G
  • Recombinant Proteins
  • Viral Proteins