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- ••TBVs are the only area of malaria researchwhere such a multi-laboratory, co-ordinated approach is being attempted. As such, this a real strength for TBVs.
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- ••Including [36] and [37], these papersprovide some of the best evidence that vaccine-induced transmission blocking immunity will persist in the field due to natural boosting.
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- ••See note for [35].
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- ••See note for [35].
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- ••The first isolation and identification of agene coding for a target antigen of malaria transmission-blocking immunity.
- TSUBOI T, KASLOW DC, CAO YM, SHIWAKU K, TORII M: Comparison of Plasmodium yoelii ookinete surface antigens with human and avian malaria parasite homologues reveals two highly conserved regions. Mal Biochem. Parasitol. (1997) 87:107–111.
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- ••Along with [56], provides the firstdemonstration of vaccine-induced transmission blocking immunity in animal models using a recombinant protein adsorbed to aluminium hydroxide adjuvant.
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- ••See note for [54].
- RAWLINGS DJ, KASLOW DC: Adjuvant-dependent immune response to malarial transmission-blocking vaccine candidate antigens. J. Exp. Med. (1992) 176:1483–1487.
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- ••One of the first recombinant protein-basedvivaxyaccines for any parasite stage. Most importantly, demonstrates that TBV development for both P falciparum and P vivax are running in parallel.
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