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

被引:45
作者
de Souza, EP
Bernardo, RR
Palatnik, M
de Sousa, CBP
机构
[1] Univ Fed Rio de Janeiro, Inst Microbiol Prof Paulo Goes, CCS, BR-21941 Rio De Janeiro, Brazil
[2] Escola Quim, Rio De Janeiro, Brazil
[3] UFRJ, Hosp Univ Clementino Fraga Filho, Fac Med, Rio De Janeiro, Brazil
关键词
murine visceral leishmaniasis; GP36; glycoprotein; native antigen; adjuvants; saponin;
D O I
10.1016/S0264-410X(01)00031-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:3104 / 3115
页数:12
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