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In Vitro Evaluation of a Soluble Leishmania Promastigote Surface Antigen as a Potential Vaccine Candidate against Human Leishmaniasis

Overview of attention for article published in PLOS ONE, May 2014
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Title
In Vitro Evaluation of a Soluble Leishmania Promastigote Surface Antigen as a Potential Vaccine Candidate against Human Leishmaniasis
Published in
PLOS ONE, May 2014
DOI 10.1371/journal.pone.0092708
Pubmed ID
Authors

Rym Chamakh-Ayari, Rachel Bras-Gonçalves, Narges Bahi-Jaber, Elodie Petitdidier, Wafa Markikou-Ouni, Karim Aoun, Javier Moreno, Eugenia Carrillo, Poonam Salotra, Himanshu Kaushal, Narender Singh Negi, Jorge Arevalo, Francesca Falconi-Agapito, Angela Privat, Maria Cruz, Julie Pagniez, Gérard-Marie Papierok, Faten Bel Haj Rhouma, Pilar Torres, Jean-Loup Lemesre, Mehdi Chenik, Amel Meddeb-Garnaoui

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.

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Geographical breakdown

Country Count As %
Portugal 1 1%
France 1 1%
Australia 1 1%
Brazil 1 1%
Unknown 95 96%

Demographic breakdown

Readers by professional status Count As %
Researcher 19 19%
Student > Master 19 19%
Student > Ph. D. Student 12 12%
Student > Bachelor 12 12%
Student > Doctoral Student 6 6%
Other 14 14%
Unknown 17 17%
Readers by discipline Count As %
Agricultural and Biological Sciences 26 26%
Biochemistry, Genetics and Molecular Biology 17 17%
Immunology and Microbiology 14 14%
Medicine and Dentistry 7 7%
Veterinary Science and Veterinary Medicine 5 5%
Other 8 8%
Unknown 22 22%