Evidence map›Paper›PMID 12496190›Full record

ArticleInfection and immunity2003

Intradermal infection model for pathogenesis and vaccine studies of murine visceral leishmaniasis.

Saeed Ahmed, M Colmenares, L Soong, K Goldsmith-Pestana, L Munstermann, R Molina, Diane McMahon-Pratt

Abstract readEvaluation Study
In one paragraph

Article in Infection and immunity, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

57 citing papers in PubMed, 129 citations in OpenAlex.

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  20. Cross-species genetic exchange between visceral and cutaneous strains of Leishmania in the sand fly vector.Proceedings of the National Academy of Sciences of the United States of America · 2014
    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

7 authors at 3 institutions in 2 countries.

Saeed AhmedDepartment of Epidemiology and Public Health, Yale University School of Medicine, New Haven, Connecticut 06520-8034, USA.
M Colmenares
L Soong
K Goldsmith-Pestana
L Munstermann
R Molina
Diane McMahon-Pratt
Yale University · USCentro Nacional de Microbiologia · ESThe University of Texas Medical Branch at Galveston · US

Funding

PATHOGENIC MECHANISMS OF CUTANEOUS LEISHMANIASISR01AI043003 · NIAID · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI SOONG, LYNN · 1999 to 2010
$2.3M
VISCERAL LEISHMANIASIS VACCINE - MURINE MODEL STUDIESR01AI045044 · NIAID · YALE UNIVERSITY · PI MCMAHON PRATT, DIANE · 2000 to 2003
$1.3M
Pathogenic Mechanisms of Cutaneous LeishmaniasisR56AI043003 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI SOONG, LYNN · 2012 to 2012
$306k
NIAID NIH HHS AI43003NIAID NIH HHS AI-45044NIAID NIH HHS R01 AI043003NIAID NIH HHS R01 AI045044NIAID NIH HHS R56 AI043003
6 · The paper itself

Abstract

The levels of protection found in vaccine studies of murine visceral leishmaniasis are significantly lower than for cutaneous leishmaniasis; whether this is due to the high-challenge murine model employed and/or is a consequence of differences required in tissue-specific local immune responses is not understood. Consequently, an intradermal murine model of visceral leishmaniasis has been explored. Intradermal inoculation established a chronic infection in susceptible mice which was associated with a pattern of parasite clearance with time postinfection in the liver and skin; in contrast, parasite persistence and expansion was observed in lymphoid tissue (spleen and draining lymph node). The course of disease found appears to be similar to those reported for subclinical canine and human visceral leishmaniasis. Clearance of parasites from the skin was correlated with an inflammatory response and the infiltration and activation of CD4(+) and CD8(+) T cells. In contrast, in lymphoid tissue (lymph node or spleen), the production of Th1/Th2 cytokines (interleukin-4 [IL-4], IL-10, and gamma interferon) appeared to correlate with parasite burden and pathogenesis. In vaccination experiments employing the Leishmania infantum D-13 (p80) antigen, significantly higher levels of protection were found with the intradermal murine model (29 to 7,500-fold more than naive controls) than were found with a low-dose intravenous infection model (9 to 173-fold). Thus, this model should prove useful for further investigation of disease pathogenesis as well as vaccine studies of visceral leishmaniasis.

Indexed as

Disease Models, AnimalProtozoan VaccinesAdministration, CutaneousAnimalsAntigens, ProtozoanHumansInjections, IntravenousLeishmania infantumLeishmaniasis, VisceralLymphoid TissueMiceMice, Inbred BALB CSkinVirulenceAntigens, ProtozoanProtozoan Vaccines

Identifiers

PMID12496190
PMCPMC143149
OpenAlexW2129514368

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.