Evidence map›Paper›PMID 19388946›Full record

ReviewParasite immunology2009

Genetics and visceral leishmaniasis: of mice and man.

J M Blackwell, M Fakiola, M E Ibrahim, S E Jamieson, S B Jeronimo, E N Miller, A Mishra, H S Mohamed, C S Peacock, M Raju and 2 more

Abstract readReview
In one paragraph

Review in Parasite immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
11.4field-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

50 citing papers in PubMed, 1 synthesis or guideline pooled it, 116 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. IFN-λ3 is induced byInfection and immunity · 2024
    Article
  7. Article
  8. Review
  9. Review
  10. Role of Cytokines in Experimental and Human Visceral Leishmaniasis.Frontiers in cellular and infection microbiology · 2021
    Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Challenges in drug discovery targeting TriTryp diseases with an emphasis on leishmaniasis.International journal for parasitology. Drugs and drug resistance · 2018
    Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Cutaneous Manifestations of Human and Murine Leishmaniasis.International journal of molecular sciences · 2017
    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

12 authors at 7 institutions in 6 countries.

J M BlackwellTelethon Institute for Child Health Research, Centre for Child Health Research, The University of Western Australia, Western Australia, Australia. jblackwell@ichr.uwa.edu.au
M Fakiola
M E Ibrahim
S E Jamieson
S B Jeronimo
E N Miller
A Mishra
H S Mohamed
C S Peacock
M Raju
S Sundar
M E Wilson
University of Cambridge · GBUniversidade Federal do Rio Grande do Norte · BRUniversity of Khartoum · SDUniversity of Western Australia · AUBanaras Hindu University · INThe Kids Research Institute Australia · AUUniversity of Iowa · US

Funding

The role of Leishmania braziliensis strain polymorphism on disease outcome and ..P50AI030639 · NIAID · FEDERAL UNIVERSITY OF BAHIA · PI CARVALHO, EDGAR M · 1991 to 2023
$9.1M
Visceral Leishmaniasis in Bihar State, IndiaP50AI074321 · NIAID · BANARAS HINDU UNIVERSITY · PI SUNDAR, SHYAM · 2007 to 2016
$6.4M
Visceral Leishmaniasis in Bihar State, IndiaU19AI074321 · NIAID · BANARAS HINDU UNIVERSITY · PI RAI, MADHUKAR · 2017 to 2021
$2.8M
Genetic Risk Factors for Visceral LeishmaniasisR01AI076233 · NIAID · UNIVERSITY OF IOWA · PI BLACKWELL, JENEFER MARY, WILSON, MARY E · 2009 to 2013
$1.6M
NIAID NIH HHS P50 AI030639NIAID NIH HHS P50 AI074321NIAID NIH HHS R01 AI076233NIAID NIH HHS U19 AI074321Wellcome Trust
6 · The paper itself

Abstract

Ninety per cent of the 500,000 annual new cases of visceral leishmaniasis (VL) occur in India/Bangladesh/Nepal, Sudan and Brazil. Importantly, 80-90% of human infections are sub-clinical or asymptomatic, usually associated with strong cell-mediated immunity. Understanding the environmental and genetic risk factors that determine why two people with the same exposure to infection differ in susceptibility could provide important leads for improved therapies. Recent research using candidate gene association analysis and genome-wide linkage studies (GWLS) in collections of families from Sudan, Brazil and India have identified a number of genes/regions related both to environmental risk factors (e.g. iron), as well as genes that determine type 1 vs. type 2 cellular immune responses. However, until now all of the allelic association studies carried out have been underpowered to find genes of small effect sizes (odds ratios or OR < 2), and GWLS using multicase pedigrees have only been powered to find single major genes, or at best oligogenic control. The accumulation of large DNA banks from India and Brazil now makes it possible to undertake genome-wide association studies (GWAS), which are ongoing as part of phase 2 of the Wellcome Trust Case Control Consortium. Data from this analysis should seed research into novel genes and mechanisms that influence susceptibility to VL.

Indexed as

Genetic Predisposition to DiseaseGenome, HumanGenome-Wide Association StudyAnimalsAsia, WesternBrazilHumansHypersensitivity, DelayedLeishmania donovaniLeishmaniasis, VisceralMiceMice, Inbred BALB CSudan

Identifiers

PMID19388946
PMCPMC3160815
OpenAlexW2099408858

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.