Humoral immune response to Plasmodium falciparum vaccine candidate GMZ2 and its components in populations naturally exposed to seasonal malaria in Ethiopia

• Published in: Malaria journal 2013-02, Vol.12 (1), p.51-51, Article 51
• Main Authors: Mamo, Hassen, Esen, Meral, Ajua, Anthony, Theisen, Michael, Mordmüller, Benjamin, Petros, Beyene
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Aged; Aged, 80 and over; Amino acids; Analysis; Antibodies, Protozoan - blood; Antigens; Antigens, Protozoan - immunology; Child; Child, Preschool; Colleges & universities; Confidence intervals; Cross-Sectional Studies; Enzyme-Linked Immunosorbent Assay; Enzymes; Epidemics; Ethiopia; Ethnic Groups; Female; Glutamate; Health aspects; Humans; Immune response; Immunoglobulin G; Immunoglobulin G - blood; Infant; Infant, Newborn; Infection; Infections; Insecticides; Malaria; Malaria vaccine; Malaria Vaccines - immunology; Malaria, Falciparum - immunology; Male; Medical research; Medicine, Experimental; Middle Aged; Physiological aspects; Plasmodium falciparum; Plasmodium falciparum - immunology; Prevalence studies (Epidemiology); Proteins; Vaccines; Young Adult
• ISSN: 1475-2875; 1475-2875
• DOI: 10.1186/1475-2875-12-51

In Ethiopia, the general population is vulnerable to unpredictable epidemics of Plasmodium falciparum malaria. However, there is little information on the anti-malaria immune profile of the population in the endemic regions of the country. The study was designed to investigate the nature of humoral immune response to malaria in two ethnic groups in two endemic localities: Shewa Robit in north, and Boditi in south Ethiopia which are characterized by varying levels of malaria transmission and altitude. In a cross-sectional study, the study participants were diagnosed for malaria infection microscopically and by the rapid diagnostic test (RDT). Sera were tested by using enzyme-linked immunosorbent assay (ELISA) for total immunoglobulin (Ig) G against P. falciparum blood-stage vaccine candidate GMZ2 and its subunits (Glutamate-rich protein (GLURP-R0), merozoite surface protein 3 (MSP3); as well as IgG subclasses against GLURP-R0 and MSP3. Whereas 23(8.6%) blood smear-positive cases for P. falciparum were detected in Boditi, all Shewa Robit study participants had no detectable P. falciparum infection. In both localities, total IgG prevalence and levels to GMZ2 were significantly higher than the response to the component domains indicating the strong recognition of GMZ2 by antibodies acquired through natural exposure. Total IgG and subclass prevalence and levels were higher in Shewa Robit than Boditi, suggesting difference in the intensity of malaria transmission in the two localities and/or genetic differences between the two populations in their response to the antigens. In both study sites, IgG subclass levels to GLURP-R0 were significantly higher than that to MSP3 for all corresponding subclasses in most individuals, indicating the higher relative antigenicity and probably protective potential of GLURP-R0 compared to MSP3. Against both GLURP-R0 and MSP3, the ratio of cytophilic to noncytophilic antibodies was >1 in the majority of the study participants, in both study sites, suggesting the induction of protective (cytophilic) antibodies against the two antigens. Analysis of age-related pattern in antibody levels against the antigens showed a positive association with increasing age. P. falciparum GLURP-R0 and MSP3 separately as well as in a fused form in GMZ2 are readily recognized by the sera of the study populations. The significantly higher antibody prevalence and level detected against GMZ2 compared to either of its subunits separately, in naturally expo