Evidence map›Paper›PMID 38252221›Full record

ArticleMolecular biology reports2024

Pathogen recognition pathway gene variants and inflammasome sensors gene expression in tuberculosis patients under treatment.

Maria Eduarda Albuquerque Borborema, Ariane Fernandes da Silva Santos, Thays Maria Costa de Lucena, Sergio Crovella, Michelle Christiane da Silva Rabello, Jaqueline de Azevêdo Silva

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Article in Molecular biology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

6 authors.

Maria Eduarda Albuquerque BorboremaLaboratory of Human Genetics and Molecular Biology, Department of Genetics, Center for Biosciences, Federal University of Pernambuco, Av. Prof. Moraes Rego, 1235, Recife, PE, 50670-901 - CEP, Brazil.
Ariane Fernandes da Silva SantosLaboratory of Human Genetics and Molecular Biology, Department of Genetics, Center for Biosciences, Federal University of Pernambuco, Av. Prof. Moraes Rego, 1235, Recife, PE, 50670-901 - CEP, Brazil.
Thays Maria Costa de LucenaLaboratory of Human Genetics and Molecular Biology, Department of Genetics, Center for Biosciences, Federal University of Pernambuco, Av. Prof. Moraes Rego, 1235, Recife, PE, 50670-901 - CEP, Brazil.
Sergio CrovellaKeizo Asami Institute, Federal University of Pernambuco, Recife, PE, 50740-465 - CEP, Brazil.
Michelle Christiane da Silva RabelloAggeu Magalhães Research Institute (FIOCRUZ/IPqAM), Federal University of Pernambuco, Recife, PE, 50740-465 - CEP, Brazil.
Jaqueline de Azevêdo SilvaLaboratory of Human Genetics and Molecular Biology, Department of Genetics, Center for Biosciences, Federal University of Pernambuco, Av. Prof. Moraes Rego, 1235, Recife, PE, 50670-901 - CEP, Brazil. jaqueline.azevedo@ufpe.br.

Funding

Fundação de Amparo à Ciência e Tecnologia do Estado de Pernambuco APQ 0952-2.02/15
6 · The paper itself

Abstract

backgroundSeveral epidemiological studies have suggested that genetic variations in encoding pattern recognition receptors (PRRs) genes such as Toll Like Receptors (TLRs) and their signaling products, may influence the susceptibility, severity and outcome of tuberculosis (TB). After sensing a pathogen, the cell responds producing an inflammatory response, to restrain the pathogen's successful course of infection. Herein we assessed single nucleotide polymorphisms (SNP) and gene expression from pathogen recognition and inflammasome pathways in Brazilian TB patients. METHODS AND

resultsFor genetic association analysis we included MYD88 and TLR4, PRRs sensing proteins. Allele distribution for MYD88 rs6853 (A > G) and TLR4 rs7873784 (C > G) presented conserved among the tested samples with statistically differential distribution in TB patients versus controls. However, when testing according to sample ethnicity (African or Caucasian-derived individuals) we identified that the rs6853 G/G genotype was associated with a lower susceptibility to TB in Caucasian population. Meanwhile, the rs7873784 G/G genotype was associated with a higher TB susceptibility in Afro-descendant ethnicity individuals. We also aimed to verify MYD88 and the inflammasome genes NLRP1 and NLRC4 expression in order to connect to active TB and/or clinical aspects.

conclusionsWe identified that inflammasome gene expression in TB patients under treatment display a similar pattern as in healthy controls, indicating that TB treatment impairs NLRP1 inflammasome activation.

Indexed as

InflammasomesMyeloid Differentiation Factor 88Adaptor Proteins, Signal TransducingGene ExpressionHumansToll-Like Receptor 4Adaptor Proteins, Signal TransducingInflammasomesMyeloid Differentiation Factor 88Toll-Like Receptor 4InflammasomeMyD88NLRC4NLRP1TLR4

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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.