Evidence map›Paper›PMID 32051036›Full record

ArticleInfectious diseases of poverty2020

Serological evidence of Toxoplasma gondii infection as potential risk for the development of lepromatous leprosy in an endemic area for both neglected tropical diseases in Brazil.

Luciana Regina Pereira Oliveira, Lívia Mattos Martins, Rebeka da Conceição Souza, Yuri Scheidegger de Castro, Letícia Silva Nascimento, Juliana Azevedo da Silva, Edilbert Pellegrini Nahn Junior, Wilmar Dias da Silva, Alba Lucínia Peixoto-Rangel

Open access · goldAbstract read
In one paragraph

Article in Infectious diseases of poverty, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 48% 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, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Seroprevalence and Risk Factors ofFrontiers in cellular and infection microbiology · 2021
    Article
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 2 institutions in 1 country.

Luciana Regina Pereira OliveiraLaboratory of Recognition Biology, Center of Biosciences and Biotechnology, State University of Northern Rio de Janeiro, Campos dos Goytacazes, RJ, Brazil.
Lívia Mattos MartinsLaboratory of Recognition Biology, Center of Biosciences and Biotechnology, State University of Northern Rio de Janeiro, Campos dos Goytacazes, RJ, Brazil.
Rebeka da Conceição SouzaLaboratory of Recognition Biology, Center of Biosciences and Biotechnology, State University of Northern Rio de Janeiro, Campos dos Goytacazes, RJ, Brazil.
Yuri Scheidegger de CastroLaboratory of Recognition Biology, Center of Biosciences and Biotechnology, State University of Northern Rio de Janeiro, Campos dos Goytacazes, RJ, Brazil.
Letícia Silva NascimentoLaboratory of Recognition Biology, Center of Biosciences and Biotechnology, State University of Northern Rio de Janeiro, Campos dos Goytacazes, RJ, Brazil.
Juliana Azevedo da SilvaLaboratory of Recognition Biology, Center of Biosciences and Biotechnology, State University of Northern Rio de Janeiro, Campos dos Goytacazes, RJ, Brazil.
Edilbert Pellegrini Nahn JuniorCampos Medical School, Campos dos Goytacazes, RJ, Brazil.
Wilmar Dias da SilvaLaboratory of Recognition Biology, Center of Biosciences and Biotechnology, State University of Northern Rio de Janeiro, Campos dos Goytacazes, RJ, Brazil.
Alba Lucínia Peixoto-RangelLaboratory of Recognition Biology, Center of Biosciences and Biotechnology, State University of Northern Rio de Janeiro, Campos dos Goytacazes, RJ, Brazil. alba@uenf.br.ORCID http://orcid.org/0000-0001-6172-166X
Prefeitura Municipal de Campos dos Goytacazes · BRInstituto Butantan · BR

Funding

Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro APQ-1 E-26/111.196/2014
6 · The paper itself

Abstract

backgroundMycobacterium leprae and Toxoplasma gondii infections are both neglected tropical diseases highly prevalent in Brazil. Infection with certain parasite species can significantly alter susceptibility to other important pathogens, and/or influence the development of pathology. Here we investigated the possible influence of M. leprae/T. gondii co-parasitism on the manifestation of leprosy and its clinical forms.

methodsParticipants (n = 291) were recruited in Campos dos Goytacazes city, Rio de Janeiro state, southeast Brazil, from August 2015 to December 2019 and clinically diagnosed for leprosy. Participants were selected based on the presence (patients) or absence (healthy controls) of the leprosy disease. Contacts of patients were also recruited for this study. Serum samples from patients (n = 199) with leprosy, contacts (n = 40) and healthy controls (n = 52) were investigated for levels of IgM and IgG anti-phenolic glycolipid-1 (PGL-1) by ELISA. Additionally, IgG antibody against soluble Toxoplasma antigen (STAg) was measured in sera samples from leprosy patients, contacts and healthy controls for Toxoplasma gondii serology by ELISA. Anti-PGL-1 IgG and IgM levels were compared using one-way ANOVA Kruskal-Wallis or Mann-Whitney, while Spearman test was used to correlate levels of IgG anti-STAg and IgM/IgG anti-PGL-1 from seropositive and seronegative individuals for T. gondii infection. The risk of T. gondii infection for leprosy disease was assessed using Fisher's test.

resultsLevels of IgM anti-PGL-1 antibodies were significantly higher in multibacillary (MB) patients compared to paucibacillary (PB) patients (P = 0.0068). Higher IgM and IgG levels anti-PGL-1 were detected in patients with the lepromatous forms. The serologic prevalence for T. gondii infection was 74.9%. We detected increased anti-STAg antibody levels in leprosy patients (79.4%), reaching 88.8% within those with lepromatous form of this disease. The leprosy risk increase in T. gondii seropositive individuals was two-fold (odds ratio [OR] = 2.055; 95% confidence intervals [95% CI]: 1.18-3.51) higher than those seronegative, and considering the lepromatous leprosy risk this increase was even dramatic (OR = 4.33; 95% CI: 1.76-9.69) in T. gondii seropositive individuals. Moreover the leprosy risk in T. gondii seropositive individuals was weakly correlated to the levels of IgG anti-STAg and IgM/IgG anti-PGL-1.

conclusionsAltogether, our results suggest that T. gondii infection may exert immunomodulatory properties that influence to the susceptibility of leprosy, mainly on its more severe clinical form. A better understanding of parasite immunomodulation can ultimately contribute to the development of medical applications.

Indexed as

AdolescentAdultAgedAged, 80 and overAntibodies, BacterialBrazilCase-Control StudiesChildComorbidityEnzyme-Linked Immunosorbent AssayFemaleGlycolipidsHumansImmunoglobulin GImmunoglobulin MLeprosy, LepromatousAntibodies, BacterialGlycolipidsImmunoglobulin GImmunoglobulin MCo-immunomodulationCoinfectionImmune responseImmunoglobulinsLeprosyToxoplasmosis

Identifiers

PMID32051036
PMCPMC7017566
OpenAlexW3005566901

What OpenQuestion holds

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LicenceCC BY
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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.