Evidence map›Paper›PMID 27255376›Full record

ArticleMalaria journal2016

Immunogenetic markers associated with a naturally acquired humoral immune response against an N-terminal antigen of Plasmodium vivax merozoite surface protein 1 (PvMSP-1).

Gustavo Capatti Cassiano, Adriana A C Furini, Marcela P Capobianco, Luciane M Storti-Melo, Maria E Almeida, Danielle R L Barbosa, Marinete M Póvoa, Paulo A Nogueira, Ricardo L D Machado

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. IgM antibody responses againstFrontiers in cellular and infection microbiology · 2023
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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

9 authors at 5 institutions in 1 country.

Gustavo Capatti CassianoDepartment of Biology, São Paulo State University, São José Do Rio Preto, São Paulo, Brazil. gcapatti@hotmail.com.
Adriana A C FuriniDepartment of Skin, Infectious and Parasitic Diseases, São José do Rio Preto Medical School, São José Do Rio Preto, São Paulo, Brazil.
Marcela P CapobiancoDepartment of Biology, São Paulo State University, São José Do Rio Preto, São Paulo, Brazil.
Luciane M Storti-MeloDepartment of Biology, Federal University of Sergipe, São Cristóvão, Sergipe, Brazil.
Maria E AlmeidaLeônidas and Maria Deane Institute, Oswaldo Cruz Foundation, Manaus, Amazonas, Brazil.
Danielle R L BarbosaLaboratory of Malaria Basic Research, Division of Parasitology, Evandro Chagas Institute, Belém, Pará, Brazil.
Marinete M PóvoaLaboratory of Malaria Basic Research, Division of Parasitology, Evandro Chagas Institute, Belém, Pará, Brazil.
Paulo A NogueiraLeônidas and Maria Deane Institute, Oswaldo Cruz Foundation, Manaus, Amazonas, Brazil.
Ricardo L D MachadoDepartment of Biology, São Paulo State University, São José Do Rio Preto, São Paulo, Brazil.
Faculdade de Medicina de São José do Rio Preto · BRFundação Oswaldo Cruz · BRInstituto Evandro Chagas · BRUniversidade Estadual Paulista (Unesp) · BRUniversidade Federal de Sergipe · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHumoral immune responses against proteins of asexual blood-stage malaria parasites have been associated with clinical immunity. However, variations in the antibody-driven responses may be associated with a genetic component of the human host. The objective of the present study was to evaluate the influence of co-stimulatory molecule gene polymorphisms of the immune system on the magnitude of the humoral immune response against a Plasmodium vivax vaccine candidate antigen.

methodsPolymorphisms in the CD28, CTLA4, ICOS, CD40, CD86 and BLYS genes of 178 subjects infected with P. vivax in an endemic area of the Brazilian Amazon were genotyped by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). The levels of IgM, total IgG and IgG subclasses specific for ICB2-5, i.e., the N-terminal portion of P. vivax merozoite surface protein 1 (PvMSP-1), were determined by enzyme-linked immuno assay. The associations between the polymorphisms and the antibody response were assessed by means of logistic regression models.

resultsAfter correcting for multiple testing, the IgG1 levels were significantly higher in individuals recessive for the single nucleotide polymorphism rs3116496 in CD28 (p = 0.00004). Furthermore, the interaction between CD28 rs35593994 and BLYS rs9514828 had an influence on the IgM levels (p = 0.0009).

conclusionsThe results of the present study support the hypothesis that polymorphisms in the genes of co-stimulatory components of the immune system can contribute to a natural antibody-driven response against P. vivax antigens.

Indexed as

Polymorphism, GeneticAdolescentAdultAgedAntibodies, ProtozoanAntigens, ProtozoanBrazilCross-Sectional StudiesFemaleGenotyping TechniquesHumansImmunogeneticsImmunoglobulin GImmunoglobulin MImmunologic FactorsMaleAntibodies, ProtozoanAntigens, ProtozoanImmunoglobulin GImmunoglobulin MImmunologic FactorsMerozoite Surface Protein 1AntibodiesICB2-5ImmunogeneticsMSP-1Plasmodium vivax

Identifiers

PMID27255376
PMCPMC4891883
OpenAlexW2409513649

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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.