Improvement of the indirect hemagglutination test for the detection of antibodies to Streptococcus pyogenes

• Published in: Brazilian journal of medical and biological research Vol. 31; no. 8; pp. 1081 - 1089
• Main Authors: Rubinsky-Elefant, G, Hoshino-Shimizu, S, Mamizuka, E M, Asciutti, M M
• Format: Journal Article
• Language: English; Portuguese
• Published: Brazil Associação Brasileira de Divulgação Científica 01.08.1998
• Subjects: anti-streptolysin O antibodies; Antigens, Bacterial - blood; Antistreptolysin - blood; BIOLOGY; hemagglutination test; Hemagglutination Tests - methods; Humans; MEDICINE, RESEARCH & EXPERIMENTAL; Neutralization Tests - methods; Predictive Value of Tests; Sensitivity and Specificity; Streptococcal Infections - blood; Streptococcal Infections - diagnosis; Streptococcus pyogenes; Streptococcus pyogenes - immunology; anti-streptolysin O antibodies; Streptococcus pyogenes; hemagglutination test
• ISSN: 0100-879X; 1414-431X; 0100-879X; 1414-431X
• DOI: 10.1590/S0100-879X1998000800008

An indirect hemagglutination test for a seroepidemiological survey of Streptococcus pyogenes infection was standardized. This is an improved modification of the indirect hemagglutination test which utilizes an unstable reagent prepared with fresh blood cells. Two types of bacterial antigens represented by extracellular products and purified streptolysin O were assayed, but only the former antigen gave good results. Pretreatment of the bacterial antigen with 0.15 M NaOH and neutralization to pH 5.5, as well as postfixation of sensitized red cells with 0.1% glutaraldehyde at 56 degrees C for 30 min were found to be essential to give long stability to the reagent in liquid suspension, at least 9 months at 4 degrees C. A total of 564 serum samples with high, moderate and low anti-streptolysin O antibodies as determined by the neutralization assay were studied by the indirect hemagglutination test using the new reagent. The sensitivity, specificity, efficiency, positive predictive value and negative predictive value of the test in relation to the neutralization assay were 0.950, 0.975, 0.963, 0.973, and 0.955, respectively. The kappa agreement index between the two techniques was high (0.926) and ranked as "almost perfect". Antibody levels detected by both techniques also presented a high positive correlation (rs = 0.726). Five reagent batches successively produced proved to be reproducible. Thus, the improved indirect hemagglutination test seems to be useful for public health laboratories.