Evidence map›Paper›PMID 17403867›Full record

ArticleInfection and immunity2007

Reduced pathology following infection with transgenic Leishmania major expressing murine CD40 ligand.

Ann E Field, Sagie Wagage, Sean M Conrad, David M Mosser

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Effect of transgenicIranian journal of basic medical sciences · 2021
    Article
  2. Extracellular Vesicles in Trypanosomatids: Host Cell Communication.Frontiers in cellular and infection microbiology · 2020
    Review
  3. Immunology and Genetic ofJournal of research in medical sciences : the official journal of Isfahan University of Medical Sciences · 2018
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Modulation of dendritic cell function by Leishmania parasites.Journal of immunology (Baltimore, Md. : 1950) · 2008
    Review
  9. Evaluation of Apoptotic Effect of TransgenicIranian journal of parasitology
    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

4 authors at 1 institution in 1 country.

Ann E FieldUniversity of Maryland, 1103 Microbiology Building (Building 231), College Park, MD 20742, USA.
Sagie Wagage
Sean M Conrad
David M Mosser
University of Maryland, College Park · US

Funding

Innate and adaptive immune responses to LeishmaniaR01AI055576 · NIAID · UNIV OF MARYLAND, COLLEGE PARK · PI MOSSER, DAVID M · 2005 to 2009
$1.5M
Innate and adaptive immune responses to LeishmaniaR21AI055576 · NIAID · UNIVERSITY OF MARYLAND COLLEGE PK CAMPUS · PI MOSSER, DAVID M · 2004 to 2004
$334k
NIAID NIH HHS AI 055576NIAID NIH HHS R01 AI055576NIAID NIH HHS R21 AI055576
6 · The paper itself

Abstract

Leishmanization is the inoculation of live Leishmania into the host to vaccinate against subsequent infections. This approach has been largely discontinued due to safety concerns. We have previously shown that combining CD40 ligand (CD40L) with Leishmania antigen preferentially induces a type 1 immune response and provides some protection to vaccinated mice (G. Chen, P. A. Darrah, and D. M. Mosser, Infect. Immun. 69:3255-3263, 2001). In the present study, we developed transgenic L. major organisms which express and secrete the extracellular portion of CD40L (L. major CD40LE). We hypothesized that these organisms would be less virulent but more immunogenic than wild-type organisms and therefore be more effective at leishmanization. Transgenic parasites expressing CD40L mRNA and protein were developed. BALB/c mice infected with these parasites developed significantly smaller lesions containing fewer parasites than animals infected with wild-type organisms. Infection of resistant C57BL/6 mice with low doses of transgenic parasites induced a significant amount of protection against subsequent high-dose infection with wild-type organisms. These results demonstrate that transgenic organisms expressing CD40L are less virulent than wild-type organisms while retaining full immunogenicity.

Indexed as

AnimalsCD40 AntigensCD40 LigandLeishmania majorMiceMice, Inbred BALB COrganisms, Genetically ModifiedProtozoan VaccinesVaccinationCD40 AntigensCD40 LigandProtozoan Vaccines

Identifiers

PMID17403867
PMCPMC1932871
OpenAlexW2124183435

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.