Evidence map›Paper›PMID 24818662›Full record

ArticleInfection and immunity2014

Deficiency of lymph node-resident dendritic cells (DCs) and dysregulation of DC chemoattractants in a malnourished mouse model of Leishmania donovani infection.

Marwa K Ibrahim, Jeffrey L Barnes, E Yaneth Osorio, Gregory M Anstead, Fabio Jimenez, John J Osterholzer, Bruno L Travi, Seema S Ahuja, A Clinton White, Peter C Melby

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 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
1.3field-weighted citation impact, top 18% 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, 22 citations in OpenAlex.

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  9. Nutrients · 2021
    Article
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  12. Review
  13. Transcriptional Profiling of Immune-Related Genes inFrontiers in cellular and infection microbiology · 2018
    Article
  14. Review
  15. Article
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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

10 authors at 4 institutions in 2 countries.

Marwa K IbrahimDepartment of Microbiology and Immunology, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA South Texas Veterans Health Care System, San Antonio, Texas, USA Department of Microbial Biotechnology, Genetic Engineering Division, National Research Center, Giza, Egypt.
Jeffrey L BarnesSouth Texas Veterans Health Care System, San Antonio, Texas, USA Department of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
E Yaneth OsorioDepartment of Internal Medicine and Center for Tropical Diseases, University of Texas Medical Branch, Galveston, Texas, USA.
Gregory M AnsteadSouth Texas Veterans Health Care System, San Antonio, Texas, USA Department of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Fabio JimenezSouth Texas Veterans Health Care System, San Antonio, Texas, USA Department of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
John J OsterholzerDepartment of Internal Medicine, University of Michigan, and the VA Ann Arbor Healthcare System, Ann Arbor, Michigan, USA.
Bruno L TraviDepartment of Internal Medicine and Center for Tropical Diseases, University of Texas Medical Branch, Galveston, Texas, USA Department of Microbiology and Immunology, University of Texas Medical Branch at Galveston, Galveston, Texas, USA.
Seema S AhujaSouth Texas Veterans Health Care System, San Antonio, Texas, USA Department of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
A Clinton WhiteDepartment of Internal Medicine and Center for Tropical Diseases, University of Texas Medical Branch, Galveston, Texas, USA.
Peter C MelbyDepartment of Microbiology and Immunology, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA Department of Internal Medicine and Center for Tropical Diseases, University of Texas Medical Branch, Galveston, Texas, USA Department of Microbiology and Immunology, University of Texas Medical Branch at Galveston, Galveston, Texas, USA Department of Pathology, University of Texas Medical Branch at Galveston, Galveston, Texas, USA pcmelby@utmb.edu.
The University of Texas Medical Branch at Galveston · USThe University of Texas Health Science Center at San Antonio · USSouth Texas Veterans Health Care System · USVA Ann Arbor Healthcare System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malnutrition is thought to contribute to more than one-third of all childhood deaths via increased susceptibility to infection. Malnutrition is a significant risk factor for the development of visceral leishmaniasis, which results from skin inoculation of the intracellular protozoan Leishmania donovani. We previously established a murine model of childhood malnutrition and found that malnutrition decreased the lymph node barrier function and increased the early dissemination of L. donovani. In the present study, we found reduced numbers of resident dendritic cells (conventional and monocyte derived) but not migratory dermal dendritic cells in the skin-draining lymph nodes of L. donovani-infected malnourished mice. Expression of chemokines and their receptors involved in trafficking of dendritic cells and their progenitors to the lymph nodes was dysregulated. C-C chemokine receptor type 2 (CCR2) and its ligands (CCL2 and CCL7) were reduced in the lymph nodes of infected malnourished mice, as were CCR2-bearing monocytes/macrophages and monocyte-derived dendritic cells. However, CCR7 and its ligands (CCL19 and CCL21) were increased in the lymph node and CCR7 was increased in lymph node macrophages and dendritic cells. CCR2-deficient mice recapitulated the profound reduction in the number of resident (but not migratory dermal) dendritic cells in the lymph node but showed no alteration in the expression of CCL19 and CCL21. Collectively, these results suggest that the malnutrition-related reduction in the lymph node barrier to dissemination of L. donovani is related to insufficient numbers of lymph node-resident but not migratory dermal dendritic cells. This is likely driven by the altered activity of the CCR2 and CCR7 chemoattractant pathways.

Indexed as

AnimalsChemokinesDendritic CellsFemaleGene Expression ProfilingLeishmania donovaniLeishmaniasis, VisceralLymph NodesMaleMalnutritionMiceMice, Inbred BALB CReceptors, ChemokineChemokinesReceptors, Chemokine

Identifiers

PMID24818662
PMCPMC4136237
OpenAlexW2021010134

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.