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
相关论文
共 54 条
[11]   ANTIGEN-SPECIFIC IMMUNOSUPPRESSION IN VISCERAL LEISHMANIASIS IS CELL-MEDIATED [J].
CARVALHO, EM ;
BACELLAR, O ;
BARRAL, A ;
BADARO, R ;
JOHNSON, WD .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 83 (03) :860-864
[12]   IMMUNE-RESPONSE IN HEALTHY-VOLUNTEERS VACCINATED WITH KILLED LEISHMANIAL PROMASTIGOTES PLUS BCG .1. SKIN-TEST REACTIVITY, T-CELL PROLIFERATION AND INTERFERON-GAMMA PRODUCTION [J].
CASTES, M ;
BLACKWELL, J ;
TRUJILLO, D ;
FORMICA, S ;
CABRERA, M ;
ZORRILLA, G ;
RODAS, A ;
CASTELLANOS, PL ;
CONVIT, J .
VACCINE, 1994, 12 (11) :1041-1051
[13]   DOUBLE TARGETED GENE REPLACEMENT FOR CREATING NULL MUTANTS [J].
CRUZ, A ;
COBURN, CM ;
BEVERLEY, SM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (16) :7170-7174
[14]  
DESOUSA CBP, 1994, CIENCIA CULTURA, V46, P290
[15]  
ESTALOTE AC, 1995, BRAZ J MED BIOL RES, V28, P945
[16]  
FISHER RA, 1957, STAT TABLES AGR BIOL, P157
[17]   Effective immunization of mice against cutaneous leishmaniasis using an intrinsically adjuvanted synthetic lipopeptide vaccine [J].
Frankenburg, S ;
Axelrod, O ;
Kutner, S ;
Greenblatt, CL ;
Klaus, SN ;
Pirak, EA ;
McMaster, R ;
Lowell, GH .
VACCINE, 1996, 14 (09) :923-929
[18]   Vaccination with DNA encoding the immunodominant LACK parasite antigen confers protective immunity to mice infected with Leishmania major [J].
Gurunathan, S ;
Sacks, DL ;
Brown, DR ;
Reiner, SL ;
Charest, H ;
Glaichenhaus, N ;
Seder, RA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (07) :1137-1147
[19]   CELL-MEDIATED IMMUNE-RESPONSE IN INDIAN KALA AZAR AND POST-KALA AZAR DERMAL LEISHMANIASIS [J].
HALDAR, JP ;
GHOSE, S ;
SAHA, KC ;
GHOSE, AC .
INFECTION AND IMMUNITY, 1983, 42 (02) :702-707
[20]   FORMULATION OF THE PURIFIED FUSION PROTEIN OF RESPIRATORY SYNCYTIAL VIRUS WITH THE SAPONIN QS-21 INDUCES PROTECTIVE IMMUNE-RESPONSES IN BALB/C MICE THAT ARE SIMILAR TO THOSE GENERATED BY EXPERIMENTAL-INFECTION [J].
HANCOCK, GE ;
SPEELMAN, DJ ;
FRENCHICK, PJ ;
MINEOKUHN, MM ;
BAGGS, RB ;
HAHN, DJ .
VACCINE, 1995, 13 (04) :391-400