共 17 条
Comparative recognition by human IgG antibodies of recombinant proteins representing three asexual erythrocytic stage vaccine candidates of Plasmodium vivax
被引:33
作者:
Barbedo, Mayara B.
Ricci, Ricardo
Jimenez, Maria Carolina S.
Cunha, Maristela G.
Yazdani, Syed S.
Chitnis, Chetan E.
Rodrigues, Mauricio M.
Soares, Irene S.
机构:
[1] Univ Sao Paulo, Dept Anal Clin & Toxicol, Fac Ciencias Farmaceut, BR-05508900 Sao Paulo, Brazil
[2] Fed Univ Para, Dept Pathol, Ctr Ciencias Biol, BR-66059 Belem, Para, Brazil
[3] Int Ctr Genet Engn & Biotechnol, Malaria Res Grp, New Delhi, India
[4] Univ Fed Sao Paulo, Dept Microbiol Imunol & Parasitol, Escola Paulista Med, Sao Paulo, Brazil
来源:
MEMORIAS DO INSTITUTO OSWALDO CRUZ
|
2007年
/
102卷
/
03期
关键词:
malaria;
Plasmodium vivax;
merozoite antigens;
IgG antibody response;
D O I:
10.1590/S0074-02762007005000040
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:
In previous immuno-epidemiological studies of the naturally acquired antibody responses to merozoite surface protein-1 (MSP-1) of Plasmodium vivax, we had evidence that the responses to distinct erythrocytic stage antigens could be differentially regulated. The present study was designed to compare the antibody response to three asexual erythrocytic stage antigens vaccine candidates of P. vivax. Recombinant proteins representing the 19 kDa C-terminal region of MSP-1(PvMSP(19)), apical membrane antigen n-1 ectodomain (PvAMA-1), and the region II of duffy binding protein (PvDBP-RII) were compared in their ability to bind to IgG antibodies of serum samples collected from 220 individuals from the state of Para, in the North of Brazil. During patent infection with P. vivax, the frequency of individuals with IgG antibodies to PvMSP1(19), PvAMA-1, and PvDBP-RII were 95, 72.7, and 44.5% respectively. Although the frequency of responders to PvDBP-RII was lower, this frequency increased in individuals following multiple malarial infections. Individually, the specific antibody levels did not decline significantly nine months after treatment, except to PvMSP119. Our results further confirm a complex regulation of the immune response to distinct blood stage antigens. The reason for that is presently unknown but it may contribute to the high risk of re-infection in individuals living in the endemic areas.
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页码:335 / 339
页数:5
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