Evidence map›Paper›PMID 38500881›Full record

ArticleFrontiers in immunology2024

Blocking the CTLA-4 and PD-1 pathways during pulmonary paracoccidioidomycosis improves immunity, reduces disease severity, and increases the survival of infected mice.

Nycolas Willian Preite, Bruno Montanari Borges, Valéria de Lima Kaminski, Marina Caçador Ayupe, Leonardo Mandu Gonçalves, Bianca Vieira Dos Santos, Dennyson Leandro M Fonseca, Igor Salerno Filgueiras, Caio Loureiro Salgado, Sandra Marcia Muxel and 4 more

Open access · goldAbstract 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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

11 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Exhausted T cell phenotypes in disseminated coccidioidomycosis.medRxiv : the preprint server for health sciences · 2026
    Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Observational
  11. 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

14 authors at 3 institutions in 1 country.

Nycolas Willian PreiteInstitute of Science and Technology, Federal University of São Paulo, São Paulo, Brazil.
Bruno Montanari BorgesInstitute of Science and Technology, Federal University of São Paulo, São Paulo, Brazil.
Valéria de Lima KaminskiInstitute of Science and Technology, Federal University of São Paulo, São Paulo, Brazil.
Marina Caçador AyupeDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo (USP), São Paulo, Brazil.
Leonardo Mandu GonçalvesDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo (USP), São Paulo, Brazil.
Bianca Vieira Dos SantosInstitute of Science and Technology, Federal University of São Paulo, São Paulo, Brazil.
Dennyson Leandro M FonsecaInstitute of Mathematics and Statistics (IME), University of Sao Paulo (USP), Sao Paulo, Brazil.
Igor Salerno FilgueirasDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo (USP), São Paulo, Brazil.
Caio Loureiro SalgadoDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo (USP), São Paulo, Brazil.
Sandra Marcia MuxelDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo (USP), São Paulo, Brazil.
Otavio Cabral-MarquesDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo (USP), São Paulo, Brazil.
Denise Morais da FonsecaDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo (USP), São Paulo, Brazil.
Flávio Vieira LouresInstitute of Science and Technology, Federal University of São Paulo, São Paulo, Brazil.
Vera Lúcia Garcia CalichDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo (USP), São Paulo, Brazil.
Universidade de São Paulo · BRUniversidade Federal de São Paulo · BRFederal Institute of São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint pathways, i.e., coinhibitory pathways expressed as feedback following immune activation, are crucial for controlling an excessive immune response. Cytotoxic T lymphocyte antigen-4 (CTLA-4) and programmed cell death protein-1 (PD-1) are the central classical checkpoint inhibitory (CPI) molecules used for the control of neoplasms and some infectious diseases, including some fungal infections. As the immunosuppression of severe paracoccidioidomycosis (PCM), a chronic granulomatous fungal disease, was shown to be associated with the expression of coinhibitory molecules, we hypothesized that the inhibition of CTLA-4 and PD-1 could have a beneficial effect on pulmonary PCM. To this end, C57BL/6 mice were infected with

Indexed as

ParacoccidioidomycosisAnimalsCTLA-4 AntigenImmunoglobulin GMiceMice, Inbred C57BLPatient AcuityProgrammed Cell Death 1 ReceptorCTLA-4 AntigenImmunoglobulin GProgrammed Cell Death 1 Receptorfungal clearanceimproved immunityincreased survivalPD-1 and CTLA-4 blockadeprotective effectpulmonary paracoccidioidomycosisreduced disseminationT cell responses

Identifiers

PMID38500881
PMCPMC10945025
OpenAlexW4392372275

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.