Antibody response to malaria vaccine candidates in pregnant women with Plasmodium falciparum and Schistosoma haematobium infections

• Published in: Parasite immunology Vol. 46; no. 4; pp. e13027 - n/a
• Main Authors: Frempong, Naa Adjeley, Mama, Atikatou, Adu, Bright, Kusi, Kwadwo Asamoah, Ofori, Michael F., Ahiabor, Charity, Anyan, William K., Debrah, Alex Yaw, Anang, Abraham A., Ndam, Nicaise T., Courtin, David
• Format: Journal Article
• Language: English
• Published: England Wiley Subscription Services, Inc 01.04.2024
• Subjects: Animals; Antibodies; Antibodies, Protozoan; Antibody Formation; Antibody response; Antigens, Protozoan; Female; Fetuses; Humans; Immunoglobulin G; Infections; Malaria; malaria vaccine candidates; Malaria Vaccines; Malaria, Falciparum - complications; Malaria, Falciparum - epidemiology; Malaria, Falciparum - prevention & control; Plasmodium falciparum; Pregnancy; Pregnant Women; Regression analysis; Schistosoma haematobium; Schistosomiasis haematobia - complications; Schistosomiasis haematobia - epidemiology; Schistosomiasis haematobia - prevention & control; Vaccines; antibody response; pregnant women; malaria vaccine candidates
• ISSN: 0141-9838; 1365-3024
• DOI: 10.1111/pim.13027

Malaria in pregnancy has severe consequences for the mother and foetus. Antibody response to specific malaria vaccine candidates (MVC) has been associated with a decreased risk of clinical malaria and its outcomes. We studied Plasmodium falciparum (Pf) and Schistosoma haematobium (Sh) infections and factors that could influence antibody responses to MVC in pregnant women. A total of 337 pregnant women receiving antenatal care (ANC) and 139 for delivery participated in this study. Pf infection was detected by qPCR and Sh infection using urine filtration method. Antibody levels against CSP, AMA‐1, GLURP‐R0, VAR2CSA and Pfs48/45 MVC were quantified by ELISA. Multivariable linear regression models identified factors associated with the modulation of antibody responses. The prevalence of Pf and Sh infections was 27% and 4% at ANC and 7% and 4% at delivery. Pf infection, residing in Adidome and multigravidae were positively associated with specific IgG response to CSP, AMA‐1, GLURP‐R0 and VAR2CSA. ITN use and IPTp were negatively associated with specific IgG response to GLURP‐R0 and Pfs48/45. There was no association between Sh infection and antibody response to MVC at ANC or delivery. Pf infections in pregnant women were positively associated with antibody response to CSP, GLURP‐R0 and AMA‐1. Antibody response to GLURP‐R0 and Pfs48/45 was low for IPTp and ITN users. This could indicate a lower exposure to Pf infection and low malaria prevalence observed at delivery.