Plasmodium falciparum malaria in children aged 0-2 years: the role of foetal haemoglobin and maternal antibodies to two asexual malaria vaccine candidates (MSP3 and GLURP)

• Published in: PloS one Vol. 9; no. 9; p. e107965
• Main Authors: Kangoye, David Tiga, Nebie, Issa, Yaro, Jean-Baptiste, Debe, Siaka, Traore, Safiatou, Ouedraogo, Oumarou, Sanou, Guillaume, Soulama, Issiaka, Diarra, Amidou, Tiono, Alfred, Marsh, Kevin, Sirima, Sodiomon Bienvenu, Bejon, Philip
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 19.09.2014; Public Library of Science (PLoS)
• Subjects: Antibodies; Antigens; Antigens, Protozoan - immunology; Biology and Life Sciences; Blood; Burkina Faso; Child, Preschool; Children; Chromatography; Clinics; Consent; Enzyme-Linked Immunosorbent Assay; Enzymes; Erythrocytes; Female; Fetal Hemoglobin - immunology; Glutamate; Health risks; Hemoglobin; Hemoglobins; High pressure; Humans; Immunoglobulin G; Immunoglobulins; Incidence; Infant; Infant, Newborn; Infants; Infection; Light microscopy; Liquid chromatography; Longitudinal Studies; Malaria; Malaria vaccines; Malaria Vaccines - immunology; Malaria, Falciparum - epidemiology; Malaria, Falciparum - immunology; Male; Maternal-Fetal Exchange - immunology; Medical research; Medicine; Medicine and Health Sciences; Plasmodium falciparum; Plasmodium falciparum - immunology; Plasmodium falciparum - pathogenicity; Pregnancy; Protozoan Proteins - immunology; Risk; Risk Assessment; Roofing; Studies; Vaccines; Vector-borne diseases; Burkina Faso; United Kingdom > UK; Kenya
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0107965

Children below six months are reported to be less susceptible to clinical malaria. Maternally derived antibodies and foetal haemoglobin are important putative protective factors. We examined antibodies to Plasmodium falciparum merozoite surface protein 3 (MSP3) and glutamate-rich protein (GLURP), in children in their first two years of life in Burkina Faso and their risk of malaria. A cohort of 140 infants aged between four and six weeks was recruited in a stable transmission area of south-western Burkina Faso and monitored for 24 months by active and passive surveillance. Malaria infections were detected by examining blood smears using light microscopy. Enzyme-linked immunosorbent assay was used to quantify total Immunoglobulin G to Plasmodium falciparum antigens MSP3 and two regions of GLURP (R0 and R2) on blood samples collected at baseline, three, six, nine, 12, 18 and 24 months. Foetal haemoglobin and variant haemoglobin fractions were measured at the baseline visit using high pressure liquid chromatography. A total of 79.6% of children experienced one or more episodes of febrile malaria during monitoring. Antibody titres to MSP3 were prospectively associated with an increased risk of malaria while antibody responses to GLURP (R0 and R2) did not alter the risk. Antibody titres to MSP3 were higher among children in areas of high malaria risk. Foetal haemoglobin was associated with delayed first episode of febrile malaria and haemoglobin CC type was associated with reduced incidence of febrile malaria. We did not find any evidence of association between titres of antibodies to MSP3, GLURP-R0 or GLURP-R2 as measured by enzyme-linked immunosorbent assay and early protection against malaria, although anti-MSP3 antibody titres may reflect increased exposure to malaria and therefore greater risk. Foetal haemoglobin was associated with protection against febrile malaria despite the study limitations and its role is therefore worthy further investigation.