Evidence map›Paper›PMID 39744632›Full record

ArticleFrontiers in immunology2024

The landscape of chemokine and cytokine is associated with the distinct clinical status of leprosy patients and their respective household contacts.

Lorena Bruna Pereira de Oliveira, Pedro Henrique Ferreira Marçal, Karolina Dias Campos, Daisy Cristina Monteiro Dos Santos, Marlucy Rodrigues Lima, Olindo Assis Martins-Filho, Joaquim Pedro Brito-de-Sousa, Thais Abdala-Torres, Roberta Olmo Pinheiro, Euzenir Nunes Sarno and 2 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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.

Lorena Bruna Pereira de OliveiraUniversidade Vale do Rio Doce - Univale, Governador Valadares, MG, Brazil.
Pedro Henrique Ferreira MarçalUniversidade Vale do Rio Doce - Univale, Governador Valadares, MG, Brazil.
Karolina Dias CamposUniversidade Federal de Juiz de Fora, Campus Governador Valadares, MG, Brazil.
Daisy Cristina Monteiro Dos SantosUniversidade Federal de Juiz de Fora, Campus Governador Valadares, MG, Brazil.
Marlucy Rodrigues LimaUniversidade Vale do Rio Doce - Univale, Governador Valadares, MG, Brazil.
Olindo Assis Martins-FilhoGrupo Integrado de Pesquisas em Biomarcadores, Instituto René Rachou, FIOCRUZ-Minas, Belo Horizonte, MG, Brazil.
Joaquim Pedro Brito-de-SousaGrupo Integrado de Pesquisas em Biomarcadores, Instituto René Rachou, FIOCRUZ-Minas, Belo Horizonte, MG, Brazil.
Thais Abdala-TorresGrupo Integrado de Pesquisas em Biomarcadores, Instituto René Rachou, FIOCRUZ-Minas, Belo Horizonte, MG, Brazil.
Roberta Olmo PinheiroLaboratório de Hanseníase, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz -FIOCRUZ-RJ, Rio de Janeiro, RJ, Brazil.
Euzenir Nunes SarnoLaboratório de Hanseníase, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz -FIOCRUZ-RJ, Rio de Janeiro, RJ, Brazil.
Jessica K FairleyDivision of Infectious Diseases, Department of Medicine, School of Medicine, Emory University, Atlanta, GA, United States.
Lucia Alves de Oliveira FragaPrograma Multicêntrico de Bioquímica e Biologia Molecular/PMBqBM - Universidade Federal de Juiz de Fora - UFJF, Governador Valadares, MG, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Leprosy, a chronic infectious disease, is closely linked to the host immune response. According to the WHO, leprosy patients (L) and household contacts (HHC) are classified into subgroups: paucibacillary (PB) and multibacillary (MB), witch reflect the degree of infection in patients and the level of exposure of their contacts. The main goal of this study was to: i) establish a comprehensive overview of soluble mediator signatures of PBMCs upon Methods: Long-term PBMC cultures were carried out and supernatants collected for 12 CH and CY analisys by Cytometric Beads Array. Results and discussion: The CH and CY analysis, using continuous variable modeling, demonstrated that PBMCs from both L and HHC exhibited high levels of TNF upon M. leprae-stimuli. While lower production of IFN-γ were observed for L, low levels of CXCL8 was found for HHC. Soluble mediator signatures, analyzed using categorical variables, revealed that while high levels of TNF were observed for L, high levels of IFN-γ appeared as a hallmark of HHC. Overall, these analyses demonstrated that CXCL8, IFN-γ, and TNF were key markers differentiating L from HHC and endemic control (EC), especially considering the categorical analysis of the soluble mediator signatures. Data further demonstrated that higher levels of IFN-γ and lower levels CXCL8 was features associated with HHC(MB), whereas high levels of TNF were observed in both L subgroups. Moreover, data from integrative networks, based on correlation amongst soluble mediators, revealed that in M. leprae-stimuli, the number of correlations was lower in HHC(MB) compared to HHC(PB), but higher in L(MB) compared to L(PB). It was noted that the number of correlations decreased in the following order: EC > L > HHC. Our findings contribute to additional immunological features associated with L and HHC, witch can be useful complementary diagnostic/prognostic tools for classification of L and HHC, providing insights to enrich the research agenda about the hypothesis that HHC should be closely monitored as they may present a subclinical infection.

Indexed as

CytokinesLeprosyMycobacterium lepraeAdultAgedBiomarkersCells, CulturedChemokinesFamily CharacteristicsFemaleHumansLeukocytes, MononuclearMaleMiddle AgedYoung AdultBiomarkersChemokinesCytokineschemokinescytokineshousehold contactsleprosyMycobacterium leprae

Identifiers

PMID39744632
PMCPMC11688302

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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.