Evidence map›Paper›PMID 25360558›Full record

ArticlePloS one2014

An analysis of the binding characteristics of a panel of recently selected ICAM-1 binding Plasmodium falciparum patient isolates.

Aymen M Madkhali, Mohammed O Alkurbi, Tadge Szestak, Anja Bengtsson, Pradeep R Patil, Yang Wu, Saeed A Al-Harthi, Saeed Alharthi, Anja T R Jensen, Richard Pleass and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Trial
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  5. ICAM-1Malaria journal · 2022
    Article
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  7. Structural insights into diverse modes of ICAM-1 binding byProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 3 countries.

Aymen M MadkhaliDepartment of Parasitology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom; Department of Medical Laboratories Technology, College of Applied Medical Sciences, Jazan University, Jazan, Kingdom of Saudi Arabia.
Mohammed O AlkurbiDepartment of Parasitology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom; Department of Laboratory Medicine, College of Applied Medical Sciences, Umm Al-Qura University, Makkah Al-Mukarramah, Kingdom of Saudi Arabia.
Tadge SzestakDepartment of Parasitology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Anja BengtssonCentre for Medical Parasitology, Department of International Health, Immunology and Microbiology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Pradeep R PatilDepartment of Parasitology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Yang WuDepartment of Parasitology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Saeed A Al-HarthiDepartment of Parasitology, Faculty of Medicine, Umm AL-Qura University, Makkah, Kingdom of Saudia Arabia.
Saeed AlharthiDepartment of Laboratory Medicine, College of Applied Medical Sciences, Umm Al-Qura University, Makkah Al-Mukarramah, Kingdom of Saudi Arabia.
Anja T R JensenCentre for Medical Parasitology, Department of International Health, Immunology and Microbiology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Richard PleassDepartment of Parasitology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Alister G CraigDepartment of Parasitology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Liverpool School of Tropical Medicine · GBUmm al-Qura University · SAUniversity of Copenhagen · DKJazan University · SA

Funding

Medical Research Council MC_PC_12017Wellcome TrustWellcome Trust 095507
6 · The paper itself

Abstract

The basis of severe malaria pathogenesis in part includes sequestration of Plasmodium falciparum-infected erythrocytes (IE) from the peripheral circulation. This phenomenon is mediated by the interaction between several endothelial receptors and one of the main parasite-derived variant antigens (PfEMP1) expressed on the surface of the infected erythrocyte membrane. One of the commonly used host receptors is ICAM-1, and it has been suggested that ICAM-1 has a role in cerebral malaria pathology, although the evidence to support this is not conclusive. The current study examined the cytoadherence patterns of lab-adapted patient isolates after selecting on ICAM-1. We investigated the binding phenotypes using variant ICAM-1 proteins including ICAM-1Ref, ICAM-1Kilifi, ICAM-1S22/A, ICAM-1L42/A and ICAM-1L44/A using static assays. The study also examined ICAM-1 blocking by four anti-ICAM-1 monoclonal antibodies (mAb) under static conditions. We also characterised the binding phenotypes using Human Dermal Microvascular Endothelial Cells (HDMEC) under flow conditions. The results show that different isolates have variant-specific binding phenotypes under both static and flow conditions, extending our previous observations that this variation might be due to variable contact residues on ICAM-1 being used by different parasite PfEMP1 variants.

Indexed as

Biological AssayCell AdhesionDermisEndothelial CellsHumansIntercellular Adhesion Molecule-1Mutant ProteinsPlasmodium falciparumProtein BindingIntercellular Adhesion Molecule-1Mutant Proteins

Identifiers

PMID25360558
PMCPMC4216080
OpenAlexW1993399508

What OpenQuestion holds

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Registered trials

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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.