Assuntos
Infecções Oportunistas Relacionadas com a AIDS/imunologia , Soropositividade para HIV/imunologia , Malária Falciparum/imunologia , Infecções Oportunistas Relacionadas com a AIDS/diagnóstico , Infecções Oportunistas Relacionadas com a AIDS/epidemiologia , Adolescente , Adulto , Animais , Anticorpos Antiprotozoários/análise , Western Blotting , Brasil/epidemiologia , Reações Cruzadas , Ensaio de Imunoadsorção Enzimática/métodos , Feminino , Anticorpos Anti-HIV/análise , Soropositividade para HIV/diagnóstico , Soropositividade para HIV/epidemiologia , Humanos , Malária Falciparum/diagnóstico , Malária Falciparum/epidemiologia , Masculino , Pessoa de Meia-Idade , Plasmodium falciparum/imunologia , Reação em Cadeia da Polimerase/métodosRESUMO
The objective of the present study is to standardize the technical variables for preparation and storage of Plasmodium falciparum and of antigen components extracted with the amphoteric detergent Zwittergent. P. falciparum obtained from in vitro culture was stored at different temperatures and for different periods of time. For each variable, antigen components of the parasite were extracted in the presence or absence of protease inhibitors and submitted or not to later dialysis. Products were stored for 15, 30 and 60 days at different temperatures and immunological activity of each extract was determined by SDS-PAGE and ELISA using positive or negative standard sera for the presence of IgG directed to blood stage antigens of P. falciparum. Antigen extracts obtained from parasites stored at -20 degrees C up to 10 days or at -70 degrees C for 2 months presented the best results, showing well-defined bands on SDS-PAGE and Western blots and presenting absorbance values in ELISA that permitted safe differentiation between positive and negative sera.