Identification of immunodominant epitopes of Schistosoma mansoni vaccine candidate antigens using human T cells

被引:20
作者
Fonseca, CT
Cunha-Neto, E
Kalil, J
de Jesus, AR
Correa-Oliveira, R
Carvalho, E
Oliveira, S
机构
[1] Univ Fed Minas Gerais, Dept Bioquim & Imunol, Inst Invest Imunol, Inst Milenio, BR-31270901 Belo Horizonte, MG, Brazil
[2] Univ Sao Paulo, Inst Coracao, Lab Imunol, Sao Paulo, Brazil
[3] Univ Fed Bahia, Hosp Professor Edgard Santos, Serv Immunol, Salvador, BA, Brazil
[4] Fiocruz MS, Ctr Pesquisas Rene Rachou, Immunol Lab, Belo Horizonte, MG, Brazil
来源
MEMORIAS DO INSTITUTO OSWALDO CRUZ | 2004年 / 99卷 / 05期
关键词
T cells; synthetic peptides; vaccines; Schistosoma mansoni; Sm14; paramyosin;
D O I
10.1590/S0074-02762004000900011
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Paramyosin and Sm14 are two of the six antigens selected by the World Health Organization as candidates to compose a subunit vaccine against schistosomiasis. Both antigens are recognized by individuals naturally resistant to Schistosoma mansoni infection and induced protective immunity in the murine model. Three Sm14 epitopes and eleven paramyosin epitopes were selected by their ability to bind to different HLA-DR molecules using the TEPITOPE computer program, and these peptides were synthetically produced. The cellular recognition of Sm14 and paramyosin epitopes by peripheral blood mononuclear cells of individuals living in endemic area for schistosomiasis was tested by T cell proliferation assay. Among all Sm14 and paramyosin epitopes studied, Sm14-3 was Preferentially recognized by individuals naturally resistant to S. mansoni infection while Para-5 was preferentially recognized by individuals resistant to reinfection. These two peptides represent promising antigens to be used in an experimental vaccine against schistosomiasis, since their preferential recognition by resistant individuals suggest their involvement in the induction of protective immunity.
引用
收藏
页码:63 / 66
页数:4
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