Evidence map›Paper›PMID 24613206›Full record

ArticleInternational immunopharmacology2014

Immunomodulatory effects of recombinant lactoferrin during MRSA infection.

Shen-An Hwang, Marian L Kruzel, Jeffrey K Actor

Open access · greenAbstract read
In one paragraph

Article in International immunopharmacology, 2014. 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
2.3field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Modulation of TDM-induced granuloma pathology by human lactoferrin: a persistent effect in mice.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2023
    Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Innate Nutritional Immunity.Journal of immunology (Baltimore, Md. : 1950) · 2018
    Review
  13. Article
  14. Review
  15. Article
  16. Review
  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

3 authors at 1 institution in 1 country.

Shen-An HwangDepartment of Pathology, Medical School, University of Texas-Houston Medical School, Houston, TX, United States.
Marian L KruzelDepartment of Integrative Biology and Pharmacology, University of Texas-Houston Medical School, Houston, TX, United States.
Jeffrey K ActorDepartment of Pathology, Medical School, University of Texas-Houston Medical School, Houston, TX, United States. Electronic address: Jeffrey.K.Actor@uth.tmc.edu.
The University of Texas Health Science Center at Houston · US

Funding

Lactoferrin as an Adjuvant for Cellular ImmunityR42AI051050 · NIAID · PHARMAREVIEW CORPORATION · PI ACTOR, JEFFREY K · 2005 to 2010
$4.1M
Lactoferrin for Immunomodulation of Systemic Inflammatory Response SyndromeR42GM079810 · NIGMS · PHARMAREVIEW CORPORATION · PI ACTOR, JEFFREY K, KRUZEL, MARIAN L · 2010 to 2011
$1.4M
Lactoferrin for Immunomodulation of Systemic Inflammatory Response SyndromeR41GM079810 · NIGMS · PHARMAREVIEW CORPORATION · PI ACTOR, JEFFREY K · 2007 to 2008
$298k
NIAID NIH HHS R42 AI051050NIAID NIH HHS R42-AI051050-05NIGMS NIH HHS 1R41GM079810-03ANIGMS NIH HHS R41 GM079810NIGMS NIH HHS R42 GM079810
6 · The paper itself

Abstract

Methicillin-resistant Staphylococcus aureus (MRSA) infection remains a serious hazard to global health. The use of immune modulatory therapy to combat infection is gaining an interest as a novel treatment alternative. Lactoferrin (LF), an iron binding protein with immune modulating properties, has the potential to modify the course of systemic MRSA infection. Specifically, LF is capable of limiting deleterious inflammatory responses while promoting the development of antigen specific T-cell activity. The efficacy of a novel recombinant mouse LF (rmLF) to protect against MRSA infection was examined in a mouse peritonitis model. BALB/c mice were infected with a lethal dose of MRSA and treated at 2h post-infection with rmLF. Effects of rmLF on MRSA-infected primary monocytes and granulocytes were analyzed for inflammatory mediators. The rmLF treated mice demonstrated a modest increase in survival of more than 24h, albeit with reduced bacteremia. Serum cytokines, IL-17 and IL-6, were significantly reduced post-challenge post-rmLF treatment. The rmLF led to a minor decrease in IL-1b, and a slight increase in TNF-a production. Preliminary investigation towards human clinical relevance was accomplished using human blood derived monocytes and granulocytes infected with MRSA and treated with homologous recombinant human LF (rhLF). Treatment with (rhLF) led to increased production of IFN-g and IL-2. The human cell studies also showed a concurrent decrease in TNF-a, IL-6, IL-1b, IL-12p40, and IL-10. These results indicate that the rmLF and rhLF have a high degree of overlap to modify inflammatory responses, although differences in activities were observed between the two heterologous recombinant molecules.

Indexed as

AnimalsBacterial LoadCHO CellsCricetulusCytokinesGranulocytesHumansImmunologic FactorsLactoferrinMethicillin-Resistant Staphylococcus aureusMice, Inbred BALB CMonocytesPeritonitisRecombinant ProteinsSpleenStaphylococcal InfectionsCytokinesImmunologic FactorsLactoferrinLTF protein, humanLtf protein, mouseRecombinant ProteinsImmune modulationLactoferrinMRSAStaphylococcus aureus (MRSA)

Identifiers

PMID24613206
PMCPMC4017373
OpenAlexW2000398313

What OpenQuestion holds

Textmetadata
LicenceTDM
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.