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Vaccination of Balb/c mice against experimental visceral leishmaniasis with the GP36 glycoprotein antigen of Leishmania donovani.

Authors :
Paraguai de Souza E
Bernardo RR
Palatnik M
Palatnik de Sousa CB
Source :
Vaccine [Vaccine] 2001 Apr 30; Vol. 19 (23-24), pp. 3104-15.
Publication Year :
2001

Abstract

Leishmania donovani GP36 glycoprotein is the main antigen of the FML Fucose Mannose Ligand (FML) complex specifically recognized by sera of kala-azar human patients. The GP36 was isolated by chemical elution + sonication and used for Balb/c mouse vaccination in combination with saponin, by the s.c. route, inducing a strong and specific protective effect against experimental visceral leishmaniasis shown by the increase of: specific IgG antibodies (82.6%), mainly IgG2a, the delayed type of hypersensitivity to promastigote lysate (37.8%, P < 0.001), the in vitro cellular proliferative response to GP36 of ganglia lymphocytes (53.5%, P < 0.005) and the decrease of liver parasite burden (68.1%, P < 0.025). Saponin treated controls reacted significantly differently from GP36 vaccinated animals at all the assayed variables (P < 0.05). GP36 induced significant protection against murine visceral leishmaniasis at concentrations commonly used for vaccination with recombinant antigens.

Details

Language :
English
ISSN :
0264-410X
Volume :
19
Issue :
23-24
Database :
MEDLINE
Journal :
Vaccine
Publication Type :
Academic Journal
Accession number :
11312005
Full Text :
https://doi.org/10.1016/s0264-410x(01)00031-7