Evidence map›Paper›PMID 24786587›Full record

ArticlePloS one2014

In vitro evaluation of a soluble Leishmania promastigote surface antigen as a potential vaccine candidate against human leishmaniasis.

Rym Chamakh-Ayari, Rachel Bras-Gonçalves, Narges Bahi-Jaber, Elodie Petitdidier, Wafa Markikou-Ouni, Karim Aoun, Javier Moreno, Eugenia Carrillo, Poonam Salotra, Himanshu Kaushal and 12 more

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
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

24 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Rectal Administration ofTropical medicine and infectious disease · 2023
    Article
  8. Article
  9. Microorganisms · 2020
    Review
  10. Article
  11. Frontiers in chemistry · 2020
    Article
  12. Article
  13. Article
  14. Review
  15. Serological and Molecular Analysis ofThe American journal of tropical medicine and hygiene · 2017
    Article
  16. Article
  17. F1 Domain of theFrontiers in immunology · 2017
    Article
  18. Frontiers in immunology · 2017
    Article
  19. Article
  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

22 authors.

Rym Chamakh-AyariLaboratory of Medical Parasitology, Biotechnology and Biomolecules, LR11-IPT-06, Institut Pasteur de Tunis, Tunis, Tunisia.
Rachel Bras-GonçalvesInstitut de Recherche pour le Développement, UMR177 IRD/CIRAD «INTERTRYP», Montpellier, France.
Narges Bahi-JaberLaboratory of Transmission, Control and Immunobiology of Infection, LR11-IPT-02, Institut Pasteur de Tunis, Tunis, Tunisie; UPSP EGEAL Institut Polytechnique LaSalle Beauvais, Beauvais, France.
Elodie PetitdidierInstitut de Recherche pour le Développement, UMR177 IRD/CIRAD «INTERTRYP», Montpellier, France.
Wafa Markikou-OuniLaboratory of Medical Parasitology, Biotechnology and Biomolecules, LR11-IPT-06, Institut Pasteur de Tunis, Tunis, Tunisia.
Karim AounLaboratory of Medical Parasitology, Biotechnology and Biomolecules, LR11-IPT-06, Institut Pasteur de Tunis, Tunis, Tunisia.
Javier MorenoWHO Collaborating Center for Leishmaniasis, Centro Nacional de Microbiologia, Instituto de Salud Carlos III, Madrid, Spain.
Eugenia CarrilloWHO Collaborating Center for Leishmaniasis, Centro Nacional de Microbiologia, Instituto de Salud Carlos III, Madrid, Spain.
Poonam SalotraNational Institute of Pathology (ICMR), Safdarjung Hospital Campus, New Delhi, India.
Himanshu KaushalNational Institute of Pathology (ICMR), Safdarjung Hospital Campus, New Delhi, India.
Narender Singh NegiNational Institute of Pathology (ICMR), Safdarjung Hospital Campus, New Delhi, India.
Jorge ArevaloInstituto de Medicina Tropical "Alexander von Humboldt", Universidad Peruana Cayetano Heredia (UPCH), Lima, Peru.
Francesca Falconi-AgapitoInstituto de Medicina Tropical "Alexander von Humboldt", Universidad Peruana Cayetano Heredia (UPCH), Lima, Peru.
Angela PrivatInstituto de Medicina Tropical "Alexander von Humboldt", Universidad Peruana Cayetano Heredia (UPCH), Lima, Peru.
Maria CruzInstituto de Medicina Tropical "Alexander von Humboldt", Universidad Peruana Cayetano Heredia (UPCH), Lima, Peru.
Julie PagniezInstitut de Recherche pour le Développement, UMR177 IRD/CIRAD «INTERTRYP», Montpellier, France.
Gérard-Marie PapierokBVT-VIRBAC, La Seyne sur Mer, France.
Faten Bel Haj RhoumaLaboratory of Transmission, Control and Immunobiology of Infection, LR11-IPT-02, Institut Pasteur de Tunis, Tunis, Tunisie.
Pilar TorresCentro de Transfusión de la Comunidad de Madrid, Madrid, Spain.
Jean-Loup LemesreInstitut de Recherche pour le Développement, UMR177 IRD/CIRAD «INTERTRYP», Montpellier, France.
Mehdi ChenikLaboratory of Medical Parasitology, Biotechnology and Biomolecules, LR11-IPT-06, Institut Pasteur de Tunis, Tunis, Tunisia.
Amel Meddeb-GarnaouiLaboratory of Medical Parasitology, Biotechnology and Biomolecules, LR11-IPT-06, Institut Pasteur de Tunis, Tunis, Tunisia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PSA (Promastigote Surface Antigen) belongs to a family of membrane-bound and secreted proteins present in several Leishmania (L.) species. PSA is recognized by human Th1 cells and provides a high degree of protection in vaccinated mice. We evaluated humoral and cellular immune responses induced by a L. amazonensis PSA protein (LaPSA-38S) produced in a L. tarentolae expression system. This was done in individuals cured of cutaneous leishmaniasis due to L. major (CCLm) or L. braziliensis (CCLb) or visceral leishmaniasis due to L. donovani (CVLd) and in healthy individuals. Healthy individuals were subdivided into immune (HHR-Lm and HHR-Li: Healthy High Responders living in an endemic area for L. major or L. infantum infection) or non immune/naive individuals (HLR: Healthy Low Responders), depending on whether they produce high or low levels of IFN-γ in response to Leishmania soluble antigen. Low levels of total IgG antibodies to LaPSA-38S were detected in sera from the studied groups. Interestingly, LaPSA-38S induced specific and significant levels of IFN-γ, granzyme B and IL-10 in CCLm, HHR-Lm and HHR-Li groups, with HHR-Li group producing TNF-α in more. No significant cytokine response was observed in individuals immune to L. braziliensis or L. donovani infection. Phenotypic analysis showed a significant increase in CD4+ T cells producing IFN-γ after LaPSA-38S stimulation, in CCLm. A high positive correlation was observed between the percentage of IFN-γ-producing CD4+ T cells and the released IFN-γ. We showed that the LaPSA-38S protein was able to induce a mixed Th1 and Th2/Treg cytokine response in individuals with immunity to L. major or L. infantum infection indicating that it may be exploited as a vaccine candidate. We also showed, to our knowledge for the first time, the capacity of Leishmania PSA protein to induce granzyme B production in humans with immunity to L. major and L. infantum infection.

Indexed as

Adaptive ImmunityAnimalsAntigens, ProtozoanAntigens, SurfaceGranzymesHumansImmunity, HumoralInterferon-gammaInterleukin-10LeishmaniaLeishmaniasisMicePhenotypeProtozoan VaccinesSolubilityTumor Necrosis Factor-alphaAntigens, ProtozoanAntigens, SurfaceGranzymesInterferon-gammaInterleukin-10Protozoan VaccinesTumor Necrosis Factor-alpha

Identifiers

PMID24786587
PMCPMC4008367

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.