Evidence map›Paper›PMID 24154626›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

Programmed death 1-mediated T cell exhaustion during visceral leishmaniasis impairs phagocyte function.

Kevin J Esch, Rachel Juelsgaard, Pedro A Martinez, Douglas E Jones, Christine A Petersen

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 110 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
110citing papers in PubMed, 1 pooled it
12.4field-weighted citation impact, top 1% 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

110 citing papers in PubMed, 1 synthesis or guideline pooled it, 163 citations in OpenAlex.

  1. Guideline
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  6. PD-L1Frontiers in immunology · 2026
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  10. Tick-borne coinfections modulate CD8Infection and immunity · 2025
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  19. Article
  20. Article

50 more citing papers are in PubMed but not listed here.

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

5 authors at 1 institution in 1 country.

Kevin J EschDepartment of Veterinary Pathology, College of Veterinary Medicine, Iowa State University, Ames, IA 50011.
Rachel Juelsgaard
Pedro A Martinez
Douglas E Jones
Christine A Petersen
Iowa State University · US

Funding

Role of pathogen-derived capping carbohydrates in altering immunityR21AI074711 · NIAID · IOWA STATE UNIVERSITY · PI PETERSEN, CHRISTINE A · 2008 to 2010
$491k
Sand fly role in transmission of CVL in North AmericaR21AI088051 · NIAID · KANSAS STATE UNIVERSITY · PI RAMALHO-ORTIGAO, JOSE MARCELO · 2010 to 2011
$414k
Trypanosoma cruzi-elicited cardiac hypertrophyK08AI050803 · NIAID · IOWA STATE UNIVERSITY · PI PETERSEN, CHRISTINE A · 2002 to 2004
$285k
NIAID NIH HHS AI50803NIAID NIH HHS K08 AI050803NIAID NIH HHS R21 AI074711NIAID NIH HHS R21 AI088051
6 · The paper itself

Abstract

Control of Leishmania infantum infection is dependent upon Th1 CD4(+) T cells to promote macrophage intracellular clearance of parasites. Deficient CD4(+) T cell effector responses during clinical visceral leishmaniasis (VL) are associated with elevated production of IL-10. In the primary domestic reservoir of VL, dogs, we define occurrence of both CD4(+) and CD8(+) T cell exhaustion as a significant stepwise loss of Ag-specific proliferation and IFN-γ production, corresponding to increasing VL symptoms. Exhaustion was associated with a 4-fold increase in the population of T cells with surface expression of programmed death 1 (PD-1) between control and symptomatic populations. Importantly, exhausted populations of CD8(+) T cells and to a lesser extent CD4(+) T cells were present prior to onset of clinical VL. VL-exhausted T cells did not undergo significant apoptosis ex vivo after Ag stimulation. Ab block of PD-1 ligand, B7.H1, promoted return of CD4(+) and CD8(+) T cell function and dramatically increased reactive oxygen species production in cocultured monocyte-derived phagocytes. As a result, these phagocytes had decreased parasite load. To our knowledge, we demonstrate for the first time that pan-T cell, PD-1-mediated, exhaustion during VL influenced macrophage-reactive oxygen intermediate production. Blockade of the PD-1 pathway improved the ability of phagocytes isolated from dogs presenting with clinical VL to clear intracellular parasites. T cell exhaustion during symptomatic canine leishmaniasis has implications for the response to vaccination and therapeutic strategies for control of Leishmania infantum in this important reservoir species.

Indexed as

AnimalsAntibodies, BlockingB7-H1 AntigenCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCells, CulturedClonal AnergyCoculture TechniquesDogsHumansInterferon-gammaInterleukin-10Leishmania infantumLeishmaniasis, VisceralOxidative StressParasite LoadAntibodies, BlockingB7-H1 AntigenInterferon-gammaInterleukin-10Programmed Cell Death 1 ReceptorReactive Oxygen Species

Identifiers

PMID24154626
PMCPMC3896087
OpenAlexW1904163195

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.