Evidence map›Paper›PMID 23555622›Full record

ArticlePloS one2013

Ability of innate defence regulator peptides IDR-1002, IDR-HH2 and IDR-1018 to protect against Mycobacterium tuberculosis infections in animal models.

Bruno Rivas-Santiago, Julio E Castañeda-Delgado, Cesar E Rivas Santiago, Matt Waldbrook, Irma González-Curiel, Juan C León-Contreras, Jose Antonio Enciso-Moreno, Victor del Villar, Jazmin Mendez-Ramos, Robert E W Hancock and 1 more

Abstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing 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

53 citing papers in PubMed.

  1. Article
  2. Review
  3. Peptide-Based Strategies AgainstPharmaceuticals (Basel, Switzerland) · 2025
    Review
  4. Article
  5. Mini reviews in medicinal chemistry · 2025
    Review
  6. Article
  7. Review
  8. Article
  9. Frontiers in immunology · 2023
    Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Role of Antimicrobial Peptides in Treatment and Prevention of Mycobacterium Tuberculosis: A Review.International journal of peptide research and therapeutics · 2022
    Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. 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

11 authors.

Bruno Rivas-SantiagoMedical Research Unit Zacatecas, Mexican Institute of Social Security-IMSS, Zacatecas, Mexico.
Julio E Castañeda-Delgado
Cesar E Rivas Santiago
Matt Waldbrook
Irma González-Curiel
Juan C León-Contreras
Jose Antonio Enciso-Moreno
Victor del Villar
Jazmin Mendez-Ramos
Robert E W Hancock
Rogelio Hernandez-Pando

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

Tuberculosis is an ongoing threat to global health, especially with the emergence of multi drug-resistant (MDR) and extremely drug-resistant strains that are motivating the search for new treatment strategies. One potential strategy is immunotherapy using Innate Defence Regulator (IDR) peptides that selectively modulate innate immunity, enhancing chemokine induction and cell recruitment while suppressing potentially harmful inflammatory responses. IDR peptides possess only modest antimicrobial activity but have profound immunomodulatory functions that appear to be influential in resolving animal model infections. The IDR peptides HH2, 1018 and 1002 were tested for their activity against two M. tuberculosis strains, one drug-sensitive and the other MDR in both in vitro and in vivo models. All peptides showed no cytotoxic activity and only modest direct antimicrobial activity versus M. tuberculosis (MIC of 15-30 µg/ml). Nevertheless peptides HH2 and 1018 reduced bacillary loads in animal models with both the virulent drug susceptible H37Rv strain and an MDR isolate and, especially 1018 led to a considerable reduction in lung inflammation as revealed by decreased pneumonia. These results indicate that IDR peptides have potential as a novel immunotherapy against TB.

Indexed as

AnimalsAntimicrobial Cationic PeptidesAntitubercular AgentsBacterial LoadCell LineCytokinesDrug Resistance, Multiple, BacterialHumansImmunity, InnateImmunomodulationLungMiceMicrobial Sensitivity TestsMycobacterium tuberculosisPneumoniaTuberculosis, PulmonaryAntimicrobial Cationic PeptidesAntitubercular AgentsCytokinesIDR 1002innate defense regulating peptide 1018

Identifiers

PMID23555622
PMCPMC3605426

What OpenQuestion holds

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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.