A Miniaturized Assay to Evaluate <i>Plasmodium cynomolgi</i> and <i>Plasmodium knowlesi</i> as Models for Prioritizing <i>Plasmodium vivax</i> Vaccine Targets

Plasmodium vivax vaccine discovery lags behind Plasmodium falciparum due to the absence of a reliable in vitro culture system. We developed a miniature 384-well assay for the evolutionarily related parasite species Plasmodium cynomolgi and Plasmodium knowlesi, deploying it for screening invasion inhibition efficacy of antibodies elicited against 8 P. vivax proteins. All 8 antibodies showed consistent inhibition across both P. knowlesi and P. cynomolgi species, correlating with inhibition in ex vivo P. vivax isolates. The use of simian malaria parasites and this assay represent a robust, high-throughput method for prioritizing P. vivax blood-stage vaccine candidates.

Authors

Institutions

Publication Details

Journal
The Journal of Infectious Diseases
Published
2025-03-14
DOI
https://doi.org/10.1093/infdis/jiaf136
Citations
3
Primary Topic
Malaria Research and Control
Type
article
Field-Weighted Citation Impact
5.64

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A Miniaturized Assay to Evaluate Plasmodium cynomolgi and Plasmodium knowlesi as Models for Prioritizing Plasmodium vivax Vaccine Targets

Sheena Dass, Deboki Naskar, Usheer Kanjee, Marcelo U. Ferreira et al.
3 citations
The Journal of Infectious Diseases
Malaria Research and Control
5.64
article

A Miniaturized Assay to Evaluate Plasmodium cynomolgi and Plasmodium knowlesi as Models for Prioritizing Plasmodium vivax Vaccine Targets

Sheena Dass, Deboki Naskar, Usheer Kanjee, Marcelo U. Ferreira, Julian C. Rayner, Prasun Kundu
article en
3 citations

Abstract

Plasmodium vivax vaccine discovery lags behind Plasmodium falciparum due to the absence of a reliable in vitro culture system. We developed a miniature 384-well assay for the evolutionarily related parasite species Plasmodium cynomolgi and Plasmodium knowlesi, deploying it for screening invasion inhibition efficacy of antibodies elicited against 8 P. vivax proteins. All 8 antibodies showed consistent inhibition across both P. knowlesi and P. cynomolgi species, correlating with inhibition in ex vivo P. vivax isolates. The use of simian malaria parasites and this assay represent a robust, high-throughput method for prioritizing P. vivax blood-stage vaccine candidates.

The Journal of Infectious DiseasesVol. 232(4)
University of London (GB), Harvard University (US), University of Lisbon (PT), Universidade de São Paulo (BR), University of Cambridge (GB), Cambridge School (PT), Bridge University (SS), Institute for Medical Research (MY), Institute of Biomedical Science (GB)
Emory University, National Institutes of Health, National Institute of Allergy and Infectious Diseases, Office of Research Infrastructure Programs, National Institutes of Health
Good health and well-being
Openalex Percentile: Top 5%
Malaria Research and Control
5.64
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.