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Acquisition and Decay of Antibodies to Pregnancy‐Associated Variant Antigens on the Surface of<i>Plasmodium falciparum–</i>Infected Erythrocytes That Protect against Placental Parasitemia
157
Citations
23
References
2001
Year
MalariaImmunologyPlacental ParasitemiaParasite AdhesionMaternal ImmunizationHematologyPlasmodium Falciparum MalariaAntibody EngineeringPublic HealthPlacental ImmunologyParasitologyPlacental DevelopmentMaternal HealthAutoimmunityPlacental DiseaseMaternal-fetal MedicineAntibody ScreeningPlacental FunctionPregnancy‐associated Variant AntigensPathogenesisImmune WomenParasite ControlPregnancyMedicine
Otherwise clinically immune women in areas endemic for malaria are highly susceptible to Plasmodium falciparum malaria during their first pregnancy. Pregnancy-associated malaria (PAM) is characterized by placental accumulation of infected erythrocytes that adhere to chondroitin sulfate A (CSA). Susceptibility to PAM decreases with increasing parity, apparently due to acquisition of antibodies directed against the variant surface antigens (VSAs) that mediate the adhesion to CSA (VSACSA). This study found that levels of VSACSA-specific antibodies depend on endemicity, that anti-VSACSA IgG is acquired during gestation week 20, and that plasma levels of the antibodies decline during the postpartum period. There is evidence that VSACSA-specific antibodies are linked to placental infection and that high antibody levels contribute to the control of placental infection by inhibiting parasite adhesion to CSA. Data suggest that VSACSA is a target for vaccination against PAM
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