Evidence map›Paper›PMID 35732155›Full record

ArticleCell reports. Medicine2022

Plasmodium vivax malaria serological exposure markers: Assessing the degree and implications of cross-reactivity with P. knowlesi.

Rhea J Longley, Matthew J Grigg, Kael Schoffer, Thomas Obadia, Stephanie Hyslop, Kim A Piera, Narimane Nekkab, Ramin Mazhari, Eizo Takashima, Takafumi Tsuboi and 14 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports. Medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.0field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 20 citations in OpenAlex.

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  14. Naturally acquired antibody response toFrontiers in cellular and infection microbiology · 2023
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  15. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 10 institutions in 6 countries.

Rhea J LongleyPopulation Health and Immunity Division, WEHI, Parkville 3052, VIC, Australia; Department of Medical Biology, University of Melbourne, Parkville 3052, VIC, Australia. Electronic address: longley.r@wehi.edu.au.
Matthew J GriggMenzies School of Health Research and Charles Darwin University, Darwin, NT, Australia.
Kael SchofferPopulation Health and Immunity Division, WEHI, Parkville 3052, VIC, Australia.
Thomas ObadiaInstitut Pasteur, Université de Paris, Infectious Disease Epidemiology and Analytics G5 Unit, 75015, Paris, France; Institut Pasteur, Université de Paris, Bioinformatics and Biostatistics Hub, 75015, Paris, France.
Stephanie HyslopPopulation Health and Immunity Division, WEHI, Parkville 3052, VIC, Australia.
Kim A PieraMenzies School of Health Research and Charles Darwin University, Darwin, NT, Australia.
Narimane NekkabInstitut Pasteur, Université de Paris, Infectious Disease Epidemiology and Analytics G5 Unit, 75015, Paris, France.
Ramin MazhariPopulation Health and Immunity Division, WEHI, Parkville 3052, VIC, Australia; Department of Medical Biology, University of Melbourne, Parkville 3052, VIC, Australia.
Eizo TakashimaDivision of Malaria Research, Proteo-Science Center, Ehime University, Matsuyama, Japan.
Takafumi TsuboiDivision of Malaria Research, Proteo-Science Center, Ehime University, Matsuyama, Japan.
Matthias HarbersCellFree Sciences Co., Ltd., Yokohama, Japan; RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Kevin TettehLondon School of Hygiene and Tropical Medicine, London, UK.
Chris DrakeleyLondon School of Hygiene and Tropical Medicine, London, UK.
Chetan E ChitnisMalaria Parasite Biology and Vaccines Unit, Department of Parasites and Insect Vectors, Institut Pasteur, Paris, France.
Julie HealerPopulation Health and Immunity Division, WEHI, Parkville 3052, VIC, Australia; Department of Medical Biology, University of Melbourne, Parkville 3052, VIC, Australia.
Wai-Hong ThamPopulation Health and Immunity Division, WEHI, Parkville 3052, VIC, Australia; Department of Medical Biology, University of Melbourne, Parkville 3052, VIC, Australia.
Jetsumon SattabongkotMahidol Vivax Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Michael T WhiteInstitut Pasteur, Université de Paris, Infectious Disease Epidemiology and Analytics G5 Unit, 75015, Paris, France.
Daniel J CooperMenzies School of Health Research and Charles Darwin University, Darwin, NT, Australia; Department of Medicine, University of Cambridge, Cambridge, UK.
Giri S RajahramQueen Elizabeth II Hospital, Clinical Research Centre, Kota Kinabalu, Sabah, Malaysia.
Bridget E BarberMenzies School of Health Research and Charles Darwin University, Darwin, NT, Australia.
Timothy WilliamInfectious Diseases Society Kota Kinabalu Sabah, Kota Kinabalu Sabah, Malaysia; Gleneagles Hospital, Kota Kinabalu, Sabah, Malaysia.
Nicholas M AnsteyMenzies School of Health Research and Charles Darwin University, Darwin, NT, Australia.
Ivo MuellerPopulation Health and Immunity Division, WEHI, Parkville 3052, VIC, Australia; Department of Medical Biology, University of Melbourne, Parkville 3052, VIC, Australia.
The University of Melbourne · AUCharles Darwin University · AUInstitut Pasteur · FREhime University · JPLondon School of Hygiene & Tropical Medicine · GBCellFree Sciences (Japan) · JPMahidol University · THQueen Elizabeth Hospital · MYSabah Environmental Trust · MYUniversity of Cambridge · GB

Funding

Emerging zoonotic malaria in Malaysia: strengthening surveillance and evaluating population genetic structure to improve regional risk prediction toolsR01AI160457 · NIAID · INFECTIOUS DISEASE SOCIETY KOTA KINABALU · PI RAJAHRAM, GIRI · 2021 to 2025
$674k
NIAID NIH HHS R01 AI160457Wellcome Trust 208693/Z/17/Z
6 · The paper itself

Abstract

Serological markers are a promising tool for surveillance and targeted interventions for Plasmodium vivax malaria. P. vivax is closely related to the zoonotic parasite P. knowlesi, which also infects humans. P. vivax and P. knowlesi are co-endemic across much of South East Asia, making it important to design serological markers that minimize cross-reactivity in this region. To determine the degree of IgG cross-reactivity against a panel of P. vivax serological markers, we assayed samples from human patients with P. knowlesi malaria. IgG antibody reactivity is high against P. vivax proteins with high sequence identity with their P. knowlesi ortholog. IgG reactivity peaks at 7 days post-P. knowlesi infection and is short-lived, with minimal responses 1 year post-infection. We designed a panel of eight P. vivax proteins with low levels of cross-reactivity with P. knowlesi. This panel can accurately classify recent P. vivax infections while reducing misclassification of recent P. knowlesi infections.

Indexed as

MalariaMalaria, VivaxPlasmodium knowlesiHumansImmunoglobulin GPlasmodium vivaxImmunoglobulin Gantibodiesantibody cross-reactivitymalariamalaria eliminationPlasmodium knowlesiPlasmodium vivaxserological exposure markersserosurveillancespecies cross-reactivity

Identifiers

PMID35732155
PMCPMC9245056
OpenAlexW4283271026

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.