| Literature DB >> 35290467 |
Ankur Sharma1, Bethany Jenkins1, Adovi Akue1, Lynn E Lambert1, Sachy Orr-Gonzalez1, Marvin L Thomas2, Almahamoudou Mahamar3, Bacary S Diarra3, Alassane Dicko3, Michal Fried1, Patrick E Duffy1.
Abstract
Plasmodium falciparum-infected erythrocytes that display the variant surface antigen VAR2CSA bind chondroitin sulfate A (CSA) to sequester in placental intervillous spaces, causing severe sequelae for mother and offspring. Here, we establish a placental malaria (PM) monkey model. Pregnant Aotus infected with CSA-binding P. falciparum CS2 parasites during the third trimester developed pronounced sequestration of late-stage parasites in placental intervillous spaces that express VAR2CSA and bind specifically to CSA. Similar to immune multigravid women, a monkey infected with P. falciparum CS2 parasites over successive pregnancies acquired antibodies against VAR2CSA, with potent functional activity that was boosted upon subsequent pregnancy infections. Aotus also developed functional antibodies after multiple acute PM episodes and subsequent VAR2CSA immunization. In summary, P. falciparum infections in pregnant Aotus monkeys recapitulate all the prominent features of human PM infection and immunity, and this model can be useful for basic mechanistic studies and preclinical studies to qualify candidate PM vaccines. Clinical Trials Registration: NCT02471378. Published by Oxford University Press for the Infectious Diseases Society of America 2022.Entities:
Keywords: zzm321990 Aotus monkey; zzm321990 Plasmodium falciparumzzm321990 ; VAR2CSA; animal model; placental malaria
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Year: 2022 PMID: 35290467 PMCID: PMC9417121 DOI: 10.1093/infdis/jiac096
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 7.759