Key result
Modified measles ELISA detects IgM in ~100% of natural infections, strongly linked to clinical measles.
Why the study?
Evaluation of the measles virus ELISA kit to detect specific IgM as an indicator of primary measles antibody response was needed to confirm natural infection, primary vaccination, and reexposure responses.
Observational
p-value: p=<0.0001
The modified measles virus ELISA kit performs adequately for confirming natural infection and primary vaccination, and for differentiating primary and secondary antibody responses.
Modified measles IgM ELISA shows strong performance in confirmed cases; leaves open prospective validation before routine use.
Evaluation of the measles virus ELISA kit (Merck) to detect specific IgM as an indicator of primary measles antibody response was carried out. A modification of the manufacturer's cutoff value interpretation was introduced to allow for equivocal results in addition to positive and negative ones. With this modification, the test assayed gave an overall reproducibility of 96.16%. The IgM seropositivity rate for seroneutralization-confirmed measles cases was 100% for naturally infected measles subjects and 90% for primary measles vaccinated subjects. Individuals with positive neutralizing antimeasles antibodies in close contact with a confirmed measles case gave the following measles IgM ELISA results: 54.54% negative, 9.09% positive, and 36.36% equivocal, showing a booster with IgM antibody response on reexposure to the virus. Positive subjects with neutralizing antimeasles antibodies without recent contact with a measles case gave negative IgM results. IgM seropositivity was strongly associated with IgG seroconversion and clinical measles (p < 0.0001). The technique assayed performed adequately for the confirmation of both measles natural infection and primary vaccination and for the differentiation of primary and secondary antibody response, taking into account the modification in the cutoff value interpretation introduced and providing that the serum samples are obtained between days 5 and 30 after onset of rash.
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Nates et al. (1997) conducted an observational in Measles virus infection and vaccination. Measles virus ELISA kit (Merck) with modified cutoff was evaluated on IgM seropositivity rate and association with clinical measles (p=<0.0001). The modified measles virus ELISA kit detected IgM seropositivity in 100% of naturally infected and 90% of vaccinated subjects, strongly associating with clinical measles (p<0.0001).
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