| Autor: |
Wang, R, Doolan, D L, Charoenvit, Y, Hedstrom, R C, Gardner, M J, Hobart, P, Tine, J, Sedegah, M, Fallarme, V, Sacci, J B, Kaur, M, Klinman, D M, Hoffman, S L, Weiss, W R |
| Zdroj: |
Infection and Immunity; September 1998, Vol. 66 Issue: 9 p4193-202, 10p |
| Abstrakt: |
CD8(+) T cells have been implicated as critical effector cells in protective immunity against malaria parasites developing within hepatocytes. A vaccine that protects against malaria by inducing CD8(+) T cells will probably have to include multiple epitopes on the same protein or different proteins, because of parasite polymorphism and genetic restriction of T-cell responses. To determine if CD8(+) T-cell responses against multiple P. falciparum proteins can be induced in primates by immunization with plasmid DNA, rhesus monkeys were immunized intramuscularly with a mixture of DNA plasmids encoding four P. falciparum proteins or with individual plasmids. All six monkeys immunized with PfCSP DNA, seven of nine immunized with PfSSP2 DNA, and five of six immunized with PfExp-1 or PfLSA-1 DNA had detectable antigen-specific cytotoxic T lymphocytes (CTL) after in vitro restimulation of peripheral blood mononuclear cells. CTL activity was genetically restricted and dependent on CD8(+) T cells. By providing the first evidence for primates that immunization with a mixture of DNA plasmids induces CD8(+) T-cell responses against all the components of the mixture, these studies provide the foundation for multigene immunization of humans. |
| Databáze: |
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