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Infect. Immun., 05 1997, 1606-1614, Vol 65, No. 5
IS Soares, G Levitus, JM Souza, HA Del Portillo and MM Rodrigues
In this study, we evaluated the naturally acquired immune response to
Plasmodium vivax merozoite surface protein 1 (PvMSP1) in individuals with
recent clinical episodes of malaria from the state of Para, Brazil. Ten
recombinant proteins representing the first 682 amino acids (aa) of the
N-terminal region and one representing the final 111 aa of the C-terminal
region were expressed in Escherichia coli as glutathione S-transferase
fusion proteins. Both of these regions have been suggested as candidates
for development of a vaccine against Plasmodium sp. The total frequencies
of individuals with antibodies and cellular immune responses to PvMSP1 were
high (83.8 and 75%, respectively). The recombinant proteins representing
the N- and C-terminal regions were recognized by 51.4 and 64.1% of sera,
respectively. The frequency of responders to the C-terminal region
increased according to the number of previous malaria episodes, reaching
83.3% after four episodes. Cellular immune response was measured by in
vitro proliferation and gamma interferon production. Peripheral blood
mononuclear cells of 75 and 47.2% of individuals proliferated in response
to stimulation by the N- and C-terminal regions, respectively. Also, we
found that one protein representing the N terminus and a second
representing the C terminus of PvMSP1 stimulated 54.5% of individuals to
secrete gamma interferon. We concluded that PvMSP1 is immunogenic to a
large proportion of individuals exposed to malaria. Our results also
suggested that the C-terminal region of PvMSP1 containing the two epidermal
growth factor-like domains is particularly immunogenic to antibodies and T
cells during natural infection in humans.
Copyright © 1997, American Society for Microbiology
Acquired immune responses to the N- and C-terminal regions of Plasmodium vivax merozoite surface protein 1 in individuals exposed to malaria
Departamento de Patologia, Centro de Ciencias Biologicas, Universidade Federal do Para, Brazil.
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