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

Citation
Ep. De Souza et al., Vaccination of Balb/c mice against experimental visceral leishmaniasis with the GP36 glycoprotein antigen of Leishmania donovani, VACCINE, 19(23-24), 2001, pp. 3104-3115
Citations number
54
Categorie Soggetti
Veterinary Medicine/Animal Health",Immunology
Journal title
VACCINE
ISSN journal
0264410X → ACNP
Volume
19
Issue
23-24
Year of publication
2001
Pages
3104 - 3115
Database
ISI
SICI code
0264-410X(20010430)19:23-24<3104:VOBMAE>2.0.ZU;2-Q
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 experimenta l 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 p arasite burden (68.1%, P <0.025). Saponin treated controls reacted signific antly differently from GP36 vaccinated animals at all the assayed variables (P < 0.05). GP36 induced significant protection against murine visceral le ishmaniasis at concentrations commonly used For vaccination with recombinan t antigens. (C) 2001 Elsevier Science Ltd. All rights reserved.