| Literature DB >> 30988054 |
Justin Doritchamou1, Andrew Teo1, Robert Morrison1, Gunjan Arora2, Jennifer Kwan3, Javier Manzella-Lapeira2, Sarimar Medina-Maldonado4, Jean Langhorne1,5, Lars Hviid6, David L Narum1, Alassane Dicko7, Michal Fried1, Patrick E Duffy8.
Abstract
During pregnancy, Plasmodium falciparum-infected erythrocytes (IE) accumulate in the intervillous spaces of the placenta by binding to chondroitin sulfate A (CSA) and elicit inflammatory responses that are associated with poor pregnancy outcomes. Primigravidae lack immunity to IE that sequester in the placenta and thus are susceptible to placental malaria (PM). Women become resistant to PM over successive pregnancies as antibodies to placental IE are acquired. Here, we assayed plasma collected at delivery from Malian and Tanzanian women of different parities for total antibody levels against recombinant VAR2CSA antigens (FCR3 allele), and for surface reactivity and binding inhibition and opsonizing functional activities against IE using two CSA-binding laboratory isolates (FCR3 and NF54). Overall, antibody reactivity to VAR2CSA recombinant proteins and to CSA-binding IE was higher in multigravidae than in primigravidae. However, plasma from Malian gravid women reacted more strongly with FCR3 whereas Tanzanian plasma preferentially reacted with NF54. Further, acquisition of functional antibodies was variant dependent: binding inhibition of P. falciparum strain NF54 (P < 0.001) but not of the strain FCR3 increased significantly with parity, while only opsonizing activity against FCR3 (P < 0.001) increased significantly with parity. In addition, opsonizing and binding inhibition activities of plasma of multigravidae were significantly correlated in assays of FCR3 (r = 0.4, P = 0.01) but not of NF54 isolates; functional activities did not correlate in plasma from primigravidae. These data suggest that IE surface-expressed epitopes involved in each functional activity differ among P. falciparum strains. Consequently, geographic bias in circulating strains may impact antibody functions. Our study has implications for the development of PM vaccines aiming to achieve broad protection against various parasite strains.Entities:
Keywords: Plasmodium falciparum; antibody; binding inhibition; malaria; opsonizing phagocytosis; pregnancy
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Year: 2019 PMID: 30988054 PMCID: PMC6589062 DOI: 10.1128/IAI.00865-18
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.441