Evidence map›Paper›PMID 39428748›Full record

ArticleClinical and experimental immunology2025

Senescence-related genes are associated with the immunopathology signature of American tegumentary leishmaniasis lesions and may predict progression to mucosal leishmaniasis.

Carlos Henrique Fantecelle, Luciana Polaco Covre, Paola Oliveira Lopes, Isabela Valim Sarmento, Debora Decote-Ricardo, Célio Geraldo Freire-de-Lima, Herbert Leonel de Matos Guedes, Maria Inês Fernandes Pimentel, Fatima Conceição-Silva, Ana C Maretti-Mira and 7 more

Abstract read
In one paragraph

Article in Clinical and experimental immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–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

4 citing papers in PubMed.

  1. Review
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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

17 authors.

Carlos Henrique FantecelleNúcleo de Doenças Infecciosas, Universidade Federal do Espírito Santo, Vitória, Brazil.
Luciana Polaco CovreNúcleo de Doenças Infecciosas, Universidade Federal do Espírito Santo, Vitória, Brazil.
Paola Oliveira LopesNúcleo de Biotecnologia, Universidade Federal do Espírito Santo, Vitória, Brazil.
Isabela Valim SarmentoNúcleo de Biotecnologia, Universidade Federal do Espírito Santo, Vitória, Brazil.
Debora Decote-RicardoDepartamento de Veterinária, Universidade Federal Rural do Rio de Janeiro, Rio de Janeiro, Brazil.
Célio Geraldo Freire-de-LimaInstituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Herbert Leonel de Matos GuedesInstituto de Microbiologia Professor Paulo de Goes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Maria Inês Fernandes PimentelInstituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.
Fatima Conceição-SilvaInstituto Oswaldo Cruz, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.
Ana C Maretti-MiraUSC Research Center for Liver Diseases, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Valéria M BorgesInstituto Gonçalo Muniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Lucas Pedreira de CarvalhoLaboratório de Pesquisas Clínicas do Instituto Gonçalo Muniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Edgar Marcelino de CarvalhoLaboratório de Pesquisas Clínicas do Instituto Gonçalo Muniz, Fundação Oswaldo Cruz, Salvador, Brazil.
David MosserDepartment of Cell Biology and Molecular Genetics, University of Maryland, College Park, Maryland, USA.
Aloisio FalquetoDepartamento de Medicina Social, Universidade Federal do Espírito Santo, Vitoria, Brazil.
Arne N AkbarDivision of Medicine, University College London, London, UK.
Daniel Claudio Oliveira GomesNúcleo de Doenças Infecciosas, Universidade Federal do Espírito Santo, Vitória, Brazil.ORCID 0000-0002-0663-0981

Funding

Host and parasite factors promoting disease and treatment failure in Leishmania braziliensis patientsR01AI149456 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI CARVALHO, LUCAS P, SCOTT, PHILLIP · 2020 to 2023
$626k
Fundação de Amparo a Pesquisa do Espírito Santo 2022-1TCGX and 2022-H5GWQMedical Research Council (UK) MR/T015853/1National Council for Scientific and Technological Development-CNPq 402280/2022-9NIAID NIH HHS R01 AI149456NIH HHS R01-AI-149456
6 · The paper itself

Abstract

The American tegumentary leishmaniasis (ATL) is caused by protozoans of the genus Leishmania and varies from mild localized cutaneous leishmaniasis (LCL) form to more severe manifestations such as the diffuse cutaneous leishmaniasis (DCL) form and the mucosal leishmaniasis (ML) form. Previously, we demonstrated the accumulation of senescent cells in skin lesions of patients with LCL. Moreover, lesional transcriptomic analyses revealed a robust co-induction of senescence and pro-inflammatory gene signatures, highlighting the critical role of senescent T cells in orchestrating pathology. In this work we hypothesized that senescent cells might operate differently among the ATL spectrum, potentially influencing immunopathological mechanisms and clinical outcome. We analysed previously published RNA-Seq datasets of skin biopsies of healthy subjects and lesional skin from DCL patients, LCL patients, and LCL patients that, after treatment, progressed to mucosal leishmaniasis (MLP). Our findings demonstrate a robust presence of a CD8 T-cell signature associated with both LCL and MLP lesions. Moreover, both inflammatory and cytotoxic signatures were significantly upregulated, showing a strong increase in MLP and LCL groups, but not DCL. The senescence signature was elevated between LCL and MLP groups, representing the only distinguishable signature of immunopathology between them. Interestingly, our analyses further revealed the senescence signature's capacity to predict progression from LCL to mucosal forms, which was not observed with other signatures. Both the senescence-signature score and specific senescence-associated genes demonstrated an increased capacity to predict mucosal progression, with correct predictions exceeding 97% of cases. Collectively, our findings contribute to a comprehensive understanding of immunosenescence in ATL and suggest that senescence may represent the latest and most important signature of the immunopathogenisis. This highlights its potential value in predicting disease severity.

Indexed as

CD8-Positive T-LymphocytesCellular SenescenceLeishmaniaLeishmaniasis, CutaneousLeishmaniasis, MucocutaneousAdultDisease ProgressionFemaleHumansMaleMiddle AgedSkinTranscriptomeAmerican tegumentary leishmaniasisbiomarkerimmunopathogenesisimmunosenescence

Identifiers

PMID39428748
PMCPMC11771187

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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.