Measles serodiagnosis: standardization and evaluation of a dot-ELISA

Authors

  • Lourdes R. A. Vaz de Lima Instituto Adolfo Lutz; Divisão de Biologia Médica; Seção de Imunologia
  • Sumie Hoshino-Shimizu Instituto Adolfo Lutz; Divisão de Biologia Médica; Seção de Imunologia
  • Vanda A. U. F. de Souza Instituto de Medicina Tropical de São Paulo; Laboratório de Virologia e Soroepidemiologia
  • Claudio S. Pannuti Instituto de Medicina Tropical de São Paulo; Laboratório de Virologia e Soroepidemiologia
  • Heitor F. Andrade Junior Instituto de Medicina Tropical de São Paulo; Laboratório de Virologia e Soroepidemiologia
  • Laura M. Sumita Instituto de Medicina Tropical de São Paulo; Laboratório de Virologia e Soroepidemiologia
  • Antonio W. Ferreira Instituto de Medicina Tropical de São Paulo; Laboratório de Virologia e Soroepidemiologia

Keywords:

Dot-ELISA, Measles^i1^svaccinat, Serologic diagnosis

Abstract

A Dot-ELISA using a measles virus (MV) antigen obtained by sodium deoxycholate treatment was standardized and evaluated for IgM and IgG antibody detection in measles patients and measles-vaccinated subjects. A total of 192 serum samples were studied, comprising 47 from patients with acute and convalescent measles, 55 from 9-month old children prior to measles vaccination and 41 from children of the same age after vaccination, and 49 from patients with unrelated diseases. The diagnostic performances of the IgG Dot-ELISA and IgG immuno fluorescence test (IFT) were found to be close, varying from 0.97 to 1.00 in sensitivity and the specificities were maximum (1.00). Nevertheless, the sensitivity of the IgM Dot-ELISA (0.85) was higher than that (0.63) of the IgM IFT, although both assays had comparably high (1.00) specificities. The IgM Dot-ELISA in particular proved to be more sensitive in relation to other assays studied by revealing antibodies in 80.0% (12/15) of vaccinated children on the 15th day after immunization. In contrast the IgM IFT, failed to detect antibodies in the same group of vaccinated children. The stability of the MV antigen was longer than that of the IFT antigen, and the reproducibility of the Dot-Elisa was satisfactory.

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Published

1994-04-01

Issue

Section

Serology

How to Cite

Vaz de Lima, L. R. A., Hoshino-Shimizu, S., Souza, V. A. U. F. de, Pannuti, C. S., Andrade Junior, H. F., Sumita, L. M., & Ferreira, A. W. (1994). Measles serodiagnosis: standardization and evaluation of a dot-ELISA . Revista Do Instituto De Medicina Tropical De São Paulo, 36(2), 139-147. https://www.revistas.usp.br/rimtsp/article/view/29137