Evidence map›Paper›PMID 38750020›Full record

ArticleNature communications2024

CD5L as a promising biological therapeutic for treating sepsis.

Liliana Oliveira, M Carolina Silva, Ana P Gomes, Rita F Santos, Marcos S Cardoso, Ana Nóvoa, Hervé Luche, Bruno Cavadas, Irina Amorim, Fátima Gärtner and 3 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Immune Biomarkers of Islet Transplant Rejection Revealed by Synthetic Immunological Niche.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Serum CD5L Responds Positively to Selenium and Coenzyme QAntioxidants (Basel, Switzerland) · 2025
    Article
  12. Article
  13. Article
  14. Anti-DAMP therapies for acute inflammation.Frontiers in immunology · 2025
    Review
  15. CD5L associates with IgM via the J chain.Nature communications · 2024
    Article
  16. AIP56, an AB toxin secreted byFrontiers in immunology · 2024
    Article
  17. 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

13 authors.

Liliana Oliveirai3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.ORCID http://orcid.org/0000-0001-5222-7600
M Carolina Silvai3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.ORCID http://orcid.org/0009-0008-1516-5250
Ana P Gomesi3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Rita F Santosi3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Marcos S Cardosoi3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.ORCID http://orcid.org/0000-0003-0150-7359
Ana NóvoaInstituto Gulbenkian de Ciência, Oeiras, Portugal.ORCID http://orcid.org/0000-0002-5668-5630
Hervé LucheCentre d'Immunophénomique (CIPHE), Aix Marseille Université, INSERM, CNRS, 13288, Marseille, France.ORCID http://orcid.org/0000-0003-4309-8338
Bruno Cavadasi3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Irina Amorimi3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.ORCID http://orcid.org/0000-0002-2305-1631
Fátima Gärtneri3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Bernard MalissenCentre d'Immunophénomique (CIPHE), Aix Marseille Université, INSERM, CNRS, 13288, Marseille, France.ORCID http://orcid.org/0000-0003-1340-9342
Moisés MalloInstituto Gulbenkian de Ciência, Oeiras, Portugal.ORCID http://orcid.org/0000-0002-9744-0912
Alexandre M Carmoi3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal. acarmo@ibmc.up.pt.ORCID http://orcid.org/0000-0002-2508-9799

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sepsis results from systemic, dysregulated inflammatory responses to infection, culminating in multiple organ failure. Here, we demonstrate the utility of CD5L for treating experimental sepsis caused by cecal ligation and puncture (CLP). We show that CD5L's important features include its ability to enhance neutrophil recruitment and activation by increasing circulating levels of CXCL1, and to promote neutrophil phagocytosis. CD5L-deficient mice exhibit impaired neutrophil recruitment and compromised bacterial control, rendering them susceptible to attenuated CLP. CD5L

Indexed as

Apoptosis Regulatory ProteinsMice, Inbred C57BLMice, KnockoutNeutrophilsReceptors, ScavengerSepsisAnimalsCecumChemokine CXCL1Disease Models, AnimalLigationLipopolysaccharidesMiceNeutrophil InfiltrationPhagocytosisPore Forming Cytotoxic ProteinsApoptosis Regulatory ProteinsCd5l protein, mouseChemokine CXCL1LipopolysaccharidesPore Forming Cytotoxic ProteinsReceptors, ScavengerRecombinant Proteins

Identifiers

PMID38750020
PMCPMC11096381

What OpenQuestion holds

Textmetadata
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.