Evidence map›Paper›PMID 23163958›Full record

ArticleParasite immunology

Phosphatidylserine exposure on the surface of Leishmania amazonensis amastigotes modulates in vivo infection and dendritic cell function.

J L M Wanderley, P E Thorpe, M A Barcinski, L Soong

Open access · bronzeAbstract read
In one paragraph

Article in Parasite immunology. 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
0.5field-weighted citation impact, top 36% 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, 24 citations in OpenAlex.

  1. Review
  2. Surface enolase is a virulence factor ofFrontiers in microbiology · 2026
    Article
  3. Article
  4. iScience · 2022
    Article
  5. Review
  6. Article
  7. Review
  8. CD4Frontiers in cellular and infection microbiology · 2019
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. CD300f associates with IL-4 receptor α and amplifies IL-4-induced immune cell responses.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  14. Bacterial imaging and photodynamic inactivation using zinc(II)-dipicolylamine BODIPY conjugates.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2015
    Article
  15. Article
  16. Article
  17. Review
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

4 authors at 3 institutions in 2 countries.

J L M WanderleyMorphological Sciences Program, Biomedical Sciences Institute, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
P E ThorpeDepartment of Pharmacology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
M A BarcinskiParasitology Department, Biomedical Sciences Institute, University of Sao Paulo, Sao Paulo, Brazil.
L SoongDepartment of Microbiology and Immunology, Institute for Human Infections and Immunity, University of Texas Medical Branch, Galveston, TX, USA.
The University of Texas Medical Branch at Galveston · USFundação Oswaldo Cruz · BRThe University of Texas Southwestern Medical Center · US

Funding

PATHOGENIC MECHANISMS OF CUTANEOUS LEISHMANIASISR01AI043003 · NIAID · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI SOONG, LYNN · 1999 to 2010
$2.3M
Characterization of CCR5-like Molecules in LeishmaniaR21AI076849 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI SOONG, LYNN · 2008 to 2010
$565k
Pathogenic Mechanisms of Cutaneous LeishmaniasisR56AI043003 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI SOONG, LYNN · 2012 to 2012
$306k
NIAID NIH HHS AI043003NIAID NIH HHS AI076849NIAID NIH HHS R01 AI043003NIAID NIH HHS R21 AI076849NIAID NIH HHS R56 AI043003
6 · The paper itself

Abstract

Leishmania amazonensis parasites can cause diverse forms of leishmaniasis in humans and persistent lesions in most inbred strains of mice. In both cases, the infection is characterized by a marked immunosuppression of the host. We previously showed that amastigote forms of the parasite make use of surface-exposed phosphatidylserine (PS) molecules to infect host cells and promote alternative macrophage activation, leading to uncontrolled intracellular proliferation of the parasites. In this study, we demonstrated that treatment of infected mice with a PS-targeting monoclonal antibody ameliorated parasite loads and lesion development, which correlated with increased proliferative responses by lymphocytes. In addition, we observed an enhanced dendritic cell (DC) activation and antigen presentation in vitro. Our data imply that the recognition of PS exposed on the surface of amastigotes plays a role in down-modulating DC functions, in a matter similar to that of apoptotic cell clearance. This study provides new information regarding the mechanism of immune suppression in Leishmania infection.

Indexed as

AnimalsDendritic CellsDisease Models, AnimalFemaleImmune EvasionImmune ToleranceLeishmania mexicanaMicePhosphatidylserinesPhosphatidylserines

Identifiers

PMID23163958
PMCPMC3565004
OpenAlexW2025547277

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.