Evidence map›Paper›PMID 18725797›Full record

ReviewCurrent opinion in infectious diseases2008

Recent developments leading toward a paradigm switch in the diagnostic and therapeutic approach to human leishmaniasis.

Albert Schriefer, Mary E Wilson, Edgar M Carvalho

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in infectious diseases, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
5.1field-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

29 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Benzimidazole Derivatives as New and Selective Inhibitors of Arginase fromInternational journal of molecular sciences · 2021
    Article
  6. Article
  7. Review
  8. Concentration of 2'C-methyladenosine triphosphate byThe Journal of biological chemistry · 2018
    Article
  9. Article
  10. Cutaneous Manifestations of Human and Murine Leishmaniasis.International journal of molecular sciences · 2017
    Review
  11. Article
  12. Comparative genomics of Tunisian Leishmania major isolates causing human cutaneous leishmaniasis with contrasting clinical severity.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2017
    Article
  13. Type I interferons induced by endogenous or exogenous viral infections promote metastasis and relapse of leishmaniasis.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  14. Article
  15. Phenotypic and functional characteristics of HLA-DRJournal of leukocyte biology · 2017
    Article
  16. Article
  17. Article
  18. Article
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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

3 authors at 2 institutions in 2 countries.

Albert SchrieferServiço de Imunologia, Hospital Universitário Professor Edgard Santos, Federal Unviersity of Bahia, Salvador, Bahia, Brazil.
Mary E Wilson
Edgar M Carvalho
Complexo Hospitalar Universitário Professor Edgard Santos · BRUniversity 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
Immunogenetics of Leishmania chagasi InfectionR01AI048822 · NIAID · UNIVERSITY OF IOWA · PI WILSON, MARY EDYTHE · 2001 to 2005
$3.2M
Protective Immunity to Leishmania chagasiR01AI045540 · NIAID · UNIVERSITY OF IOWA · PI WILSON, MARY E · 2001 to 2011
$3.1M
Collaborative Development of a Vaccine against Cutaneous and Visceral LeishmaniasR01AI067874 · NIAID · UNIVERSITY OF IOWA · PI WILSON, MARY E · 2006 to 2010
$2.2M
NIAID NIH HHS AI-30639NIAID NIH HHS P50 AI030639NIAID NIH HHS R01 AI045540NIAID NIH HHS R01 AI048822NIAID NIH HHS R01 AI067874
6 · The paper itself

Abstract

purpose of reviewTo identify recent papers showing how human and parasite genetics influence leishmaniasis, and how understanding of the immunopathology may be utilized in immunotherapy for these diseases. RECENT

findingsProgress has been made in recent years showing the complexity within populations of Leishmania spp. and indicating that different strains lead to diverse clinical pictures and responses to treatment. Thus detection of parasite genetic tags for the precise identification of infecting strains, and for predictive diagnosis of clinical and therapeutic fates seems now possible. Host genetic loci involved in disease outcome have been detected, which may also be explored for better case management. These developments in diagnosis will demand expanding the therapeutic arsenal to take their expected effect. This is starting to be fulfilled by immunotherapies successfully employed to treat cases refractory to standard first line drugs, as the result of a more profound comprehension of the immunopathology of the leishmaniases. SUMMARY: The knowledge mounting has already helped explain why different patients present different forms of leishmaniasis and respond differently to treatment, and may be on the verge of catalyzing a major change in the already over a century old paradigm of diagnosing and managing these patients.

Indexed as

ImmunotherapyLeishmaniasis VaccinesAnimalsHumansLeishmaniaLeishmaniasisProtozoan VaccinesLeishmaniasis VaccinesProtozoan Vaccines

Identifiers

PMID18725797
PMCPMC2593452
OpenAlexW2119733059

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.