Abstract
This paper describes the production and characterization of two monoclonal antibodies against P. falciparum soluble proteins. One of the monoclonal antibodies indentified as M-45 detected one protein of 72 kd and two more of 30 and 26 kd in a P. falciparum schizont extract, by immnoelectroblotting. The other one, G-172 detected a protein of 120 Kd. Moreover, the two monoclonal antibodies showed different immunofluorescence patterns, both recognized Schizont infected erytrocytes: M-45 (M isotype) produced a generalized and uniform fluorescence, while G-172 (G2 a isotype) produced patches of higher intensity in some regions of the schizont. Later on, M-45 and G- 172 were used in an ELISA sandwich technique as capture antibodies for P. falciparum soluble antigens. Culture supernatants and five malaria infection sera were assayed. The results showed a 100% sensibility and specificity when the dilution sera was 1/20 and 80% sensibility for the 1/40 dilution. According to these results, it might be feasible to use these monoclonal antibodies in an ELISA test to follow the course of malaria infection.
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