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1.
Sci. med ; 20(1)jan.-mar. 2010. tab
Article in Portuguese | LILACS | ID: lil-567153

ABSTRACT

Aims: The purpose of this study was to compare the performance of three automated immunoassays for the detection of IgM and IgG Toxoplasma gondii antibodies using sera of pregnant women living in Colombia, a Latin American country with a high seroprevalence. Methods: A total of 905 sera were tested for IgM antibodies and 914 for IgG antibodies with AxSYM, VIDAS and VIDIA immunoassays. Discrepancies were resolved by using the dye test for IgG antibodies, and the ISAGA test for IgM. Results: The overall agreement between AxSYM, VIDAS and VIDIA assays was excellent for detection of IgG and IgM antibodies, and discrepancies were relatively rare (3.6% and 5.5% of sera for IgG and IgM antibodies, respectively). The performance of the three immunoassays was similar for the detection of IgG antibodies with high sensitivity (100.00% for VIDIA, 99.59% for VIDAS, 99.38% for AxSYM) and specificity (99.04% for VIDIA, 98.82% for AxSYM, 98.57% for VIDAS). The specificity for IgM antibodies was excellent for the three immunassays (99.88% for VIDIA, 99.76% for AxSYM and VIDAS). The sensitivity of the detection of IgM antibodies was higher with VIDIA (95.12%) than with VIDAS (76.74%) and AxSYM (61.90%) assays. The correlation between IgG titers was limited between AxSYM and VIDAS assays and between AxSYM and VIDIA assays, but was excellent between VIDIA and VIDAS assays. Conclusions: Our study performed with Latin American sera confirmed the excellent specificity of AxSYM, VIDAS and VIDIA assays for the detection of IgG and IgM antibodies already reported in other countries. The sensitivity of the detection of IgG antibodies was slightly higher with VIDIA than with VIDAS and AxSYM assays. The sensitivity of the detection of IgM antibodies was higher with VIDIA than with VIDAS and AxSYM assays.


Subject(s)
Humans , Female , Pregnancy , Serologic Tests , Toxoplasmosis/diagnosis , Toxoplasmosis/epidemiology , Toxoplasmosis/immunology
2.
Sci. med ; 20(1)jan.-mar. 2010. graf
Article in Portuguese | LILACS | ID: lil-567163

ABSTRACT

Objetivos: analisar experimentalmente a evolução da resposta imune humoral nas fases aguda e crônica recente da infecção por Toxoplasma gondii e sua correlação com o parasitismo sanguíneo. Métodos: foram analisados, por 60 dias, 10 camundongos fêmeas da linhagem AS/n infectados, por via oral, com 10 cistos por animal da cepa ME-49 de Toxoplasma gondii. As coletas de sangue foram feitas a cada 3-4 dias. O parasitismo sanguíneo foi avaliado pela reação em cadeia da polimerase e os títulos de anticorpos por enzimaimunoensaio e imunofluorescência indireta. Resultados: a reação em cadeia da polimerase foi positiva em amostras com intervalos de aproximadamente 7 dias até o 28º dia, e a seguir, negativas até o 60º dia. Os soros avaliados pela imunofluorescência indireta apresentaram anticorpos IgM após o 7º dia, com pico entre o 18º e 27º dia. Após o primeiro mês os títulos foram baixos até o 60º dia. Anticorpos IgG surgiram no 14º dia e persistiram em altos títulos até o 60º dia. A cinética dos anticorpos IgG, bem como a avidez destes, demonstrou que os níveis de anticorpos aumentaram a partir do 14º dia e as porcen-tagens de avidez evoluíram com pico máximo após 28 dias, estabelecendo-se então a fase crônica da infecção. Conclusões: os dados aqui demonstrados enfatizam que taquizoítos podem estar presentes na circulação sanguínea durante toda a fase aguda da toxoplasmose, mesmo que já se tenha instalado a resposta imune protetora.


Aims: To analyze experimentally the humoral immune response in acute and recent chronic infections by Toxoplasma gondii and its correlation with the blood parasitism. Methods: Ten female mice AS/n inbred strain orally infected with 10 cysts per animal from T. gondii ME-49 strain were evaluated during 60 days. Blood collections were made in each 3-4 days. Blood parasitism was evaluated by polymerase chain reaction, and antibody titres by enzyme-linked immunosorbent assay and indirect immunofluorescence. Results: Positive polymerase chain reaction was detected around seven day-intervals until the 28th day and was negative after the 30th day pos-infection. Sera assayed by immunofluorescence presented IgM antibodies after the 7th day of infection and high titers were found between the 18th and 27th day. After 30 days, IgM titers were low until the 60th day. IgG antibodies were produced around the 14th day and were high until the 60th day. The avidity and kinetic exhibited by IgG antibody levels increased from the 14th day and the avidity percents increased with maximum peak after 28 days, establishing the chronic infection. Conclusions: These data emphasize that tachyzoites can be detected in blood during the acute phase of toxoplasmosis, even though the protective immune response was already developed.


Subject(s)
Mice , Antibodies, Protozoan , Antigens, Protozoan/blood , Parasitic Diseases , Immunoglobulin G , Immunoglobulin M , Acute-Phase Reaction , Polymerase Chain Reaction , Toxoplasma , Toxoplasmosis
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