Evidence map›Paper›PMID 32787908›Full record

ArticleParasites & vectors2020

Evaluation of a new live recombinant vaccine against cutaneous leishmaniasis in BALB/c mice.

Samira Salari, Iraj Sharifi, Ali Reza Keyhani, Pooya Ghasemi Nejad Almani

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  9. Vaccines · 2022
    Article
  10. Article
  11. Frontiers in immunology · 2022
    Article
  12. 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.

Samira SalariMedical Mycology and Bacteriology Research Center, Kerman University of Medical Sciences, Kerman, Iran.
Iraj SharifiLeishmaniasis Research Center, Kerman University of Medical Sciences, Kerman, Iran. iraj.sharifi@yahoo.com.
Ali Reza KeyhaniLeishmaniasis Research Center, Kerman University of Medical Sciences, Kerman, Iran.
Pooya Ghasemi Nejad AlmaniLeishmaniasis Research Center, Kerman University of Medical Sciences, Kerman, Iran. pooyaalmani@yahoo.com.
Kerman University of Medical Sciences · IR

Funding

National Institute for Medical Research Development 957777
6 · The paper itself

Abstract

backgroundLeishmaniasis is a serious health problem in some parts of the world. In spite of the many known leishmaniasis control measures, the disease has continued to increase in endemic areas, and no effective vaccine has been discovered.

methodsIn this study, Leishmania tarentulae was used as a living factory for the production of two LACK and KMP11 immunogenic antigens in the mice body, and safety profiles were investigated. The sequences of the KMP11 and LACK L. major antigens were synthesized in the pLEXSY-neo 2.1 plasmid and cloned into E. coli strain Top10, and after being linearized with the SwaI enzyme, they were transfected into the genome of L. tarentolae. The L. tarentolae-LACK/KMP11/EGFP in the stationary phase with CpG ODN as an adjuvant was used for vaccination in BALB/c mice. Vaccination was performed into the left footpad. Three weeks later, the booster was injected in the same manner. To examine the effectiveness of the injected vaccine, pathogenic L. major (MRHO/IR/75/ER) was injected into the right footpad of all mice three weeks following the booster vaccination. In order to assess humoral immunity, the levels of IgG1, and IgG2a antibodies before and 6 weeks after the challenge were studied in the groups. In addition, in order to investigate cellular immunity in the groups, the study measured IFN-γ, IL-5, TNF-α, IL-6 and IL-17 cytokines before, 3 weeks and 8 weeks after the challenge, and also the parasite load in the lymph node with real-time PCR.

resultsThe lowest level of the parasitic load was observed in the G1 group (mice vaccinated with L. tarentolae-LACK/KMP11/EGFP with CpG) in comparison with other groups (L. tarentolae-LACK/KMP11/EGFP +non-CpG (G2); L. tarentolae-EGFP + CpG (G3, control); L. tarentolae-EGFP + non-CpG (G4, control); and mice injected with PBS (G5, control). Moreover, the evaluation of immune response showed a delayed-type hypersensitivity towards Th1.

conclusionsAccording to the results of this study, the live recombinant vaccine of L. tarentolae-LACK/KMP11/EGFP with the CpG adjuvant reduced the parasitic load and footpad induration in infected mice. The long-term effects of this vaccine can be evaluated in volunteers as a clinical trial in future planning.

Indexed as

Leishmaniasis, CutaneousLeishmaniasis VaccinesVaccines, Live, UnattenuatedAnimalsAntibodies, ProtozoanAntigens, ProtozoanCloning, MolecularCytokinesEscherichia coliGenes, ProtozoanImmunity, HumoralImmunoglobulin GLeishmaniaLeishmania majorMembrane GlycoproteinsMiceAntibodies, ProtozoanAntigens, ProtozoanCytokinesImmunoglobulin Gkinetoplastid membrane protein 11, Leishmania donovaniLACK antigen, LeishmaniaLeishmaniasis VaccinesMembrane GlycoproteinsProtozoan ProteinsRecombinant ProteinsVaccines, Live, UnattenuatedVaccines, SyntheticKMP11 antigenLACK antigenLive recombinant vaccineL. tarentolae

Identifiers

PMID32787908
PMCPMC7425157
OpenAlexW3048943437

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.