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Published on: April 20, 2011
Detection of parvovirus B19-specific IgM by antibody capture radioimmunoassay
1Enteric and Respiratory Virus Laboratory, Central Public Health Laboratory, London, UK. bcohen@phls.co.uk
Insights
This study introduces a radioimmunoassay to detect parvovirus B19-IgM, aiding in diagnosing recent parvovirus B19 infections. The method quantifies specific IgM in patient serum using a capture assay.
Area of Science:
- Immunology
- Virology
- Diagnostic Assays
Background:
- Parvovirus B19 infections require accurate diagnostic methods for timely treatment.
- Existing diagnostic approaches may have limitations in detecting recent acute infections.
- Immunoglobulin M (IgM) is a key indicator of recent viral exposure.
Purpose of the Study:
- To describe a novel solid phase IgM-capture radioimmunoassay (MACRIA) for detecting parvovirus B19-specific IgM.
- To establish a quantitative method for diagnosing recent acute parvovirus B19 infection.
Main Methods:
- Serum IgM is captured using anti-human IgM immobilized on a solid phase.
- Detection involves adding parvovirus B19 antigen, followed by a detector system.
- The detector system utilizes a mouse monoclonal antibody to parvovirus B19 and a radiolabeled anti-mouse antibody (125I).
Main Results:
- The MACRIA protocol allows for the quantification of parvovirus B19-specific IgM.
- A calibration curve using standard B19 IgM serum enables single-dilution quantification of test sera.
- The assay is designed for the specific detection of IgM indicative of recent parvovirus B19 infection.
Conclusions:
- The described MACRIA is an effective method for identifying parvovirus B19-specific IgM.
- This assay provides a reliable tool for the diagnosis of recent acute parvovirus B19 infections.
- The quantitative nature of the assay enhances its clinical utility in parvovirus B19 diagnostics.
Abstract:
A solid phase IgM-capture radioimmunoassay (MACRIA) for the detection of parvovirus B19-IgM is described (Cohen et al., 1983, J. Hyg. Camb. 91, 113-130). IgM from a dilution of patients serum is 'captured' onto a solid phase coated by anti-human IgM. To determine whether any of the IgM is specific for parvovirus B19, B19 antigen is added followed by a detector system. In the MACRIA described here the detector system comprises a mouse monoclonal antibody to parvovirus B19 and a 125I-labelled anti-mouse antibody. A calibration curve derived from a standard B19 IgM serum is used to quantify B19 IgM using a single dilution of test sera. The purpose of the protocol is the diagnosis of recent acute infection with parvovirus B19.

