Evidence map›Paper›PMID 18675868›Full record

ArticleVaccine2008

Immunogenicity assay of the Leishmune vaccine against canine visceral leishmaniasis in Brazil.

G P Borja-Cabrera, F N Santos, F S Bauer, L E Parra, I Menz, A A Morgado, I S Soares, L M M Batista, C B Palatnik-de-Sousa

Open access · greenAbstract read
In one paragraph

Article in Vaccine, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
5.4field-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

33 citing papers in PubMed, 67 citations in OpenAlex.

  1. Review
  2. Article
  3. Advances inPathogens (Basel, Switzerland) · 2024
    Review
  4. Article
  5. Article
  6. Vaccination in Leishmaniasis: A Review Article.Iranian biomedical journal · 2022
    Article
  7. Article
  8. Review
  9. Saponins fromMolecules (Basel, Switzerland) · 2019
    Review
  10. Review
  11. The F1F3 Recombinant Chimera ofFrontiers in immunology · 2019
    Article
  12. Leishmaniasis in humans: drug or vaccine therapy?Drug design, development and therapy · 2018
    Review
  13. Biomarkers Associated WithFrontiers in cellular and infection microbiology · 2018
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

9 authors at 1 institution in 1 country.

G P Borja-CabreraInstituto de Microbiologia, Prof. Paulo de Góes, Universidade Federal do Rio de Janeiro, CCS, Cidade Universitária, Ilha do Fundão, CP 68040, CEP 21941-590 Rio de Janeiro, RJ, Brazil.
F N Santos
F S Bauer
L E Parra
I Menz
A A Morgado
I S Soares
L M M Batista
C B Palatnik-de-Sousa
Universidade Federal do Rio de Janeiro · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leishmune is the industrialized version of the FML-saponin vaccine which has been shown to develop 92-95% protection in vaccinated dogs and 76-80% vaccine efficacy against field canine visceral leishmaniasis (CVL) in Brazil. Leishmune has been proven to be safe and tolerable and a transmission-blocking vaccine which renders vaccinated dogs non-infectious to sand fly vectors. In the present investigation, 550 healthy seronegative dogs of endemic and epidemic areas of Brazil were monitored for Leishmune-induced immunogenicity during a 2-year trial. Another group of 588 untreated exposed dogs was also studied in parallel. Both groups were seronegative on day 0. The strong immunogenicity induced by Leishmune vaccine was demonstrated by the 98% of FML-seroconversion, increase in absorbencies, the 82.7% DTH positive reactions and increase in skin test size diameters, the average increase in CD8+ total lymphocytes population in blood (27.1%), expected for QS21 saponin-containing vaccine, the sustained proportions of CD4+ T cells, and the average increased proportions of CD21+ B lymphocytes (42.3%). The Leishmune-induced protection against CVL is demonstrated by the results: 98.8% asymptomatic dogs (at the end of first year) and 99% healthy survivors (at the end of the second year) among vaccinated dogs, compared to the 79.4% asymptomatic and 61% survivor dogs (p<0.001) monitored in the untreated exposed cohort. In spite of the low vaccine coverage, it was possible to detect a 66.1% (p<0.005) reduction in Belo Horizonte and an 80.2% (p<0.005) reduction in Araçatuba of the incidence of CVL among vaccinated dogs, when compared to the global incidence of CVL of each town, respectively. Our preliminary results support the potential use of Leishmune to prevent CVL epidemics.

Indexed as

Adjuvants, ImmunologicAnimalsAntigens, ProtozoanBrazilDog DiseasesDogsFlow CytometryHypersensitivity, DelayedLeishmania donovaniLeishmaniasis VaccinesLeishmaniasis, VisceralLeukocytes, MononuclearSaponinsAdjuvants, ImmunologicAntigens, ProtozoanLeishmaniasis Vaccinessaponin QA-21V1Saponins

Identifiers

PMID18675868
PMCPMC7173152
OpenAlexW2012080421

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.