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The respective advantages of complement fixation and ELISA for routine diagnosis of cytomegalovirus infection

Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]
|November 1, 1981
PubMed

Insights

Cytomegalovirus (CMV) testing using complement fixation (CF) and ELISA show positive correlation. ELISA is generally more sensitive, but CF is reliable for sequential samples; IgM/IgG ratio aids single-sample diagnosis.

Area of Science:

  • Medical diagnostics
  • Virology
  • Immunology

Background:

  • Cytomegalovirus (CMV) is a common pathogen requiring accurate diagnostic methods.
  • Complement fixation (CF) and enzyme-linked immunosorbent assay (ELISA) are serological tests for CMV infection.
  • Evaluating the comparative performance and cost-effectiveness of these diagnostic methods is crucial.

Purpose of the Study:

  • To compare the diagnostic performance of CF and ELISA for cytomegalovirus detection.
  • To assess the utility of the IgM/IgG ratio in single serum samples for diagnosing active CMV infection.
  • To describe a cost-saving method for preparing ELISA antigens.

Main Methods:

  • Performed CF and ELISA tests on 270 serum samples from hospitalized patients.
  • Analyzed the correlation between CF and ELISA results.
  • Calculated the IgM/IgG ratio for samples where only one serum was available.
  • Described a method for preparing ELISA antigen from CF antigen.

Main Results:

  • A positive correlation was observed between CF and ELISA test results for CMV.
  • ELISA demonstrated higher sensitivity than CF, with exceptions in patients with immunological disorders.
  • The IgM/IgG ratio (≥1 in 26% of patients) was useful for estimating active CMV infection from single serum samples.
  • CF is a reliable and inexpensive method when sequential sera are available.

Conclusions:

  • Both CF and ELISA are valuable for CMV diagnosis, with ELISA offering higher sensitivity.
  • The IgM/IgG ratio provides a valuable diagnostic indicator when only a single serum sample is obtainable.
  • A cost-effective method for ELISA antigen preparation was developed, making ELISA more accessible.

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