Evidence map›Paper›PMID 29115961›Full record

ArticleMalaria journal2017

Plasmodium falciparum variant erythrocyte surface antigens: a pilot study of antibody acquisition in recurrent natural infections.

Elise Schieck, E Jane Poole, Anja Rippert, Judy Peshu, Philip Sasi, Steffen Borrmann, Peter C Bull

Abstract read
In one paragraph

Article in Malaria journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Elise SchieckKenya Medical Research Institute/Wellcome Trust Research Programme, Center for Geographic Medicine Research-Coast, P. O. Box 428, Kilifi, 80108, Kenya. e.schieck@cgiar.org.ORCID 0000-0003-1756-6337
E Jane PooleInternational Livestock Research Institute, Old Naivasha Road, Nairobi, Kenya.
Anja RippertInstitute of Hygiene, University of Heidelberg School of Medicine, 69120, Heidelberg, Germany.
Judy PeshuKenya Medical Research Institute/Wellcome Trust Research Programme, Center for Geographic Medicine Research-Coast, P. O. Box 428, Kilifi, 80108, Kenya.
Philip SasiDepartment of Clinical Pharmacology, School of Medicine, Muhimbili University of Health and Allied Sciences, P.O. Box 65010, Dar es Salaam, Tanzania.
Steffen BorrmannKenya Medical Research Institute/Wellcome Trust Research Programme, Center for Geographic Medicine Research-Coast, P. O. Box 428, Kilifi, 80108, Kenya.
Peter C BullKenya Medical Research Institute/Wellcome Trust Research Programme, Center for Geographic Medicine Research-Coast, P. O. Box 428, Kilifi, 80108, Kenya.

Funding

Wellcome TrustWellcome Trust 084535Wellcome Trust 092741
6 · The paper itself

Abstract

backgroundDuring intra-erythrocytic replication Plasmodium falciparum escapes the human host immune system by switching expression of variant surface antigens (VSA). Piecemeal acquisition of variant specific antibody responses to these antigens as a result of exposure to multiple re-infections has been proposed to play a role in acquisition of naturally acquired immunity.

methodsImmunofluorescence was used to explore the dynamics of anti-VSA IgG responses generated by children to (i) primary malaria episodes and (ii) recurrent P. falciparum infections.

resultsConsistent with previous studies on anti-VSA responses, sera from each child taken at the time of recovery from their respective primary infection tended to recognize their own secondary parasites poorly. Additionally, compared to patients with reinfections by parasites of new merozoite surface protein 2 (MSP2) genotypes, baseline sera sampled from patients with persistent infections (recrudescence) tended to have higher recognition of heterologous parasites. This is consistent with the prediction that anti-VSA IgG responses may play a role in promoting chronic asymptomatic infections.

conclusionsThis pilot study validates the utility of recurrent natural malaria infections as a functional readout for examining the incremental acquisition of immunity to malaria.

Indexed as

Antigenic VariationAntigens, ProtozoanAntigens, SurfaceChild, PreschoolErythrocytesFemaleFluorescent Antibody TechniqueHumansInfantMalaria, FalciparumMalePilot ProjectsPlasmodium falciparumAntigens, ProtozoanAntigens, SurfaceAntibody aquisitionMalariaPlasmodium falciparumRecrudescent infectionRecurrent infection

Identifiers

PMID29115961
PMCPMC5678811

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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.