Evidence map›Paper›PMID 20189487›Full record

ArticleVaccine2010

Promiscuous T-cell epitopes of Plasmodium merozoite surface protein 9 (PvMSP9) induces IFN-gamma and IL-4 responses in individuals naturally exposed to malaria in the Brazilian Amazon.

J C Lima-Junior, D M Banic, T M Tran, V S E Meyer, S G De-Simone, F Santos, L C S Porto, M T Q Marques, A Moreno, J W Barnwell and 2 more

Open access · greenAbstract read
In one paragraph

Article in Vaccine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  5. Review
  6. Frontiers in immunology · 2017
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  7. Review
  8. Article
  9. Review
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  11. The evolution and diversity of a low complexity vaccine candidate, merozoite surface protein 9 (MSP-9), in Plasmodium vivax and closely related species.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2013
    Article
  12. Article
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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

12 authors at 5 institutions in 2 countries.

J C Lima-JuniorLaboratory of Immunoparasitology, Institute Oswaldo Cruz, Fiocruz, Rio de Janeiro, RJ, Brazil.
D M Banic
T M Tran
V S E Meyer
S G De-Simone
F Santos
L C S Porto
M T Q Marques
A Moreno
J W Barnwell
M R Galinski
J Oliveira-Ferreira
Emory University · USFundação Oswaldo Cruz · BRUniversidade do Estado do Rio de Janeiro · BRNational Center for Infectious Diseases · USUniversidade Federal Fluminense · BR

Funding

YNPRC NHP CLINICAL MEDICINE RESIDENCY PROGRAM - SUPPLEMENTP51RR000165 · NCRR · EMORY UNIVERSITY · PI JOHNS, MICHAEL M · 1985 to 2011
$114.0M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM008169 · NIGMS · EMORY UNIVERSITY · PI GROSS, ROBERT E · 1987 to 2021
$20.3M
MOLECULAR ANALYSIS OF PLASMODIUM VIVAX SURFACE ANTIGENSR01AI024710 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI GALINSKI, MARY R · 1987 to 2012
$5.2M
PLASMODIUM VIVAX MSP-3 AND MSP-9 AS VACCINE IMMUNOGENESR01AI055994 · NIAID · EMORY UNIVERSITY · PI GALINSKI, MARY R · 2004 to 2007
$1.6M
NCRR NIH HHS P51 RR000165NIAID NIH HHS R01 AI024710NIAID NIH HHS R01AI0555994NIAID NIH HHS R01 AI055994NIGMS NIH HHS T32 GM008169
6 · The paper itself

Abstract

Plasmodium vivax merozoite surface protein (PvMSP9) stimulates both cellular and humoral immune responses in individuals who are naturally infected by this parasite species. To identify immunodominant human T-cell epitopes in PvMSP9, we used the MHC class II binding peptide prediction algorithm ProPred. Eleven synthetic peptides representing predicted putative promiscuous T-cell epitopes were tested in IFN-gamma and IL-4 ELISPOT assays using peripheral blood mononuclear cells (PBMC) derived from 142 individuals from Rondonia State, Brazil who had been naturally exposed to P. vivax infections. To determine whether the predicted epitopes are preferentially recognized in the context of multiple alleles, MHC Class II typing of the cohort was also performed. Five synthetic peptides elicited robust cellular responses, and the overall frequencies of IFN-gamma and IL-4 responders to at least one of the promiscuous peptides were 62% and 46%, respectively. The frequencies of IFN-gamma and IL-4 responders to each peptide were not associated with a particular HLA-DRB1 allelic group since most of the peptides induced a response in individuals of 12 out of 13 studied allelic groups. The prediction of promiscuous epitopes using ProPred led to the identification of immunodominant epitopes recognized by PBMC from a significant proportion of a genetically heterogeneous population exposed to malaria infections. The combination of several such T-cell epitopes in a vaccine construct may increase the frequency of responders and the overall efficacy of subunit vaccines in genetically distinct populations.

Indexed as

AdultAllelesAnimalsBrazilEpitope MappingEpitopes, T-LymphocyteHLA-DR AntigensHLA-DRB1 ChainsHumansInterferon-gammaInterleukin-4Leukocytes, MononuclearMalaria, VivaxMembrane ProteinsPlasmodium vivaxProtozoan ProteinsEpitopes, T-LymphocyteHLA-DR AntigensHLA-DRB1 ChainsIL4 protein, humanInterferon-gammaInterleukin-4Membrane Proteinsmerozoite surface protein 9, PlasmodiumProtozoan Proteins

Identifiers

PMID20189487
PMCPMC2861348
OpenAlexW1963616056

What OpenQuestion holds

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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.