Evidence map›Paper›PMID 37395686›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2023

The Endogenous Retinoic Acid Receptor Pathway Is Exploited by Mycobacterium tuberculosis during Infection, Both In Vitro and In Vivo.

Yonne Karoline Tenório de Menezes, Carolina Eto, Joseana de Oliveira, Erica C Larson, Daniel A G B Mendes, Greicy Brisa Malaquias Dias, Murilo Delgobo, Abigail K Gubernat, Janelle L Gleim, Eduarda Laís Munari and 6 more

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2023. 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
–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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. 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

16 authors.

Yonne Karoline Tenório de MenezesLaboratory of Immunobiology, Department of Microbiology, Immunology and Parasitology, Federal University of Santa Catarina, Florianópolis, Brazil.ORCID 0000-0002-0565-9299
Carolina EtoLaboratory of Immunobiology, Department of Microbiology, Immunology and Parasitology, Federal University of Santa Catarina, Florianópolis, Brazil.
Joseana de OliveiraDepartment of Biochemistry and Immunology, Graduate Program in Basic and Applied Immunology, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, Brazil.ORCID 0000-0003-3969-7485
Erica C LarsonDepartment of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA.ORCID 0000-0001-5025-9369
Daniel A G B MendesLaboratory of Immunobiology, Department of Microbiology, Immunology and Parasitology, Federal University of Santa Catarina, Florianópolis, Brazil.ORCID 0000-0001-5655-0931
Greicy Brisa Malaquias DiasLaboratory of Immunobiology, Department of Microbiology, Immunology and Parasitology, Federal University of Santa Catarina, Florianópolis, Brazil.
Murilo DelgoboDepartment of Internal Medicine I, University Hospital Würzburg, Würzburg, Germany.ORCID 0000-0003-4010-1909
Abigail K GubernatDepartment of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Janelle L GleimDepartment of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Eduarda Laís MunariLaboratory of Immunobiology, Department of Microbiology, Immunology and Parasitology, Federal University of Santa Catarina, Florianópolis, Brazil.
Marick StarickLaboratory of Immunobiology, Department of Microbiology, Immunology and Parasitology, Federal University of Santa Catarina, Florianópolis, Brazil.ORCID 0000-0003-4227-7852
Fabienne FerreiraLaboratory of Molecular Genetics of Bacteria, Department of Microbiology, Immunology and Parasitology, Federal University of Santa Catarina, Florianópolis, Brazil.ORCID 0000-0002-6444-6007
Daniel Santos MansurLaboratory of Immunobiology, Department of Microbiology, Immunology and Parasitology, Federal University of Santa Catarina, Florianópolis, Brazil.ORCID 0000-0001-6773-9334
Diego L CostaDepartment of Biochemistry and Immunology, Graduate Program in Basic and Applied Immunology, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, Brazil.ORCID 0000-0002-9440-2814
Charles A ScangaDepartment of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA.ORCID 0000-0003-3654-5603
André BáficaLaboratory of Immunobiology, Department of Microbiology, Immunology and Parasitology, Federal University of Santa Catarina, Florianópolis, Brazil.ORCID 0000-0002-5148-600X

Funding

Effects of HIV SIV on unconventional T cells in immunity to M. tuberculosis in pre adolescentsR01AI142662 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI NDHLOVU, LISHOMWA C, OCONNOR, SHELBY L · 2019 to 2023
$6.2M
Re-educating T cell-mediated immunity in SIV by modulating metabolic pathwaysK01OD033539 · OD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LARSON, ERICA CHRISTINE · 2022 to 2024
$571k
Howard Hughes Medical Institute 55007412NIAID NIH HHS R01 AI142662NIH HHS K01 OD033539
6 · The paper itself

Abstract

Retinoic acid (RA) is a fundamental vitamin A metabolite involved in regulating immune responses through the nuclear RA receptor (RAR) and retinoid X receptor. While performing experiments using THP-1 cells as a model for Mycobacterium tuberculosis infection, we observed that serum-supplemented cultures displayed high levels of baseline RAR activation in the presence of live, but not heat-killed, bacteria, suggesting that M. tuberculosis robustly induces the endogenous RAR pathway. Using in vitro and in vivo models, we have further explored the role of endogenous RAR activity in M. tuberculosis infection through pharmacological inhibition of RARs. We found that M. tuberculosis induces classical RA response element genes such as CD38 and DHRS3 in both THP-1 cells and human primary CD14+ monocytes via a RAR-dependent pathway. M. tuberculosis-stimulated RAR activation was observed with conditioned media and required nonproteinaceous factor(s) present in FBS. Importantly, RAR blockade by (4-[(E)-2-[5,5-dimethyl-8-(2-phenylethynyl)-6H-naphthalen-2-yl]ethenyl]benzoic acid), a specific pan-RAR inverse agonist, in a low-dose murine model of tuberculosis significantly reduced SIGLEC-F+CD64+CD11c+high alveolar macrophages in the lungs, which correlated with 2× reduction in tissue mycobacterial burden. These results suggest that the endogenous RAR activation axis contributes to M. tuberculosis infection both in vitro and in vivo and reveal an opportunity for further investigation of new antituberculosis therapies.

Indexed as

Mycobacterium tuberculosisReceptors, Retinoic AcidAnimalsDrug Inverse AgonismHumansMiceRetinoid X ReceptorsTretinoinReceptors, Retinoic AcidRetinoid X ReceptorsTretinoin

Identifiers

PMID37395686
PMCPMC12462659

What OpenQuestion holds

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Registered trials

None linked

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.