Abstract |
Development of a suitable vaccine against visceral leishmaniasis (VL), a fatal parasitic disease, is considered to be vital for maintaining the success of kala-azar control programs. The fact that Leishmania-infected individuals generate life-long immunity offers a viable proposition in this direction. Our prior studies demonstrated that T-helper1 (Th1) type of cellular response was generated by six potential recombinant proteins viz. elongation factor-2 (elF-2), enolase, aldolase, triose phosphate isomerase (TPI), protein disulfide isomerase (PDI) and p45, derived from a soluble antigenic fraction (89.9-97.1 kDa) of Leishmania (Leishmania) donovani promastigote, in treated Leishmania patients and golden hamsters and showed significant prophylactic potential against experimental VL. Moreover, since, it is well-known that our immune system, in general, triggers production of specific protective immunity in response to a small number of amino acids ( peptide), this led to the identification of antigenic epitopes of the above-stated proteins utilizing immunoinformatics. Out of thirty-six, three peptides-P-10 ( enolase), P-14, and P-15 (TPI) elicited common significant lymphoproliferative as well as Th1-biased cytokine responses both in golden hamsters and human subjects. Further, immunization with these peptides plus BCG offered 75% prophylactic efficacy with boosted cellular immune response in golden hamsters against Leishmania challenge which is indicative of their candidature as potential vaccine candidates.
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Authors | Sumit Joshi, Narendra Kumar Yadav, Keerti Rawat, Vikash Kumar, Rafat Ali, Amogh Anant Sahasrabuddhe, Mohammad Imran Siddiqi, Wahajul Haq, Shyam Sundar, Anuradha Dube |
Journal | Frontiers in immunology
(Front Immunol)
Vol. 10
Pg. 288
( 2019)
ISSN: 1664-3224 [Electronic] Switzerland |
PMID | 30873164
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Cytokines
- Epitopes, T-Lymphocyte
- Leishmaniasis Vaccines
- Protozoan Proteins
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Topics |
- Animals
- Cricetinae
- Cytokines
(blood)
- Epitopes, T-Lymphocyte
(immunology)
- Leishmania donovani
(immunology)
- Leishmaniasis Vaccines
(immunology)
- Lymphocyte Activation
- Mesocricetus
- Protozoan Proteins
(immunology)
- Spleen
(immunology)
- Th1 Cells
(immunology)
- Vaccination
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