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Plasmodium vivax transmission-blocking vaccines: Progress, challenges and innovation.
Tachibana, Mayumi; Takashima, Eizo; Morita, Masayuki; Sattabongkot, Jetsumon; Ishino, Tomoko; Culleton, Richard; Torii, Motomi; Tsuboi, Takafumi.
Afiliação
  • Tachibana M; Division of Molecular Parasitology, Proteo-Science Center, Ehime University, Toon, Ehime 791-0295, Japan. Electronic address: mtachi@m.ehime-u.ac.jp.
  • Takashima E; Division of Malaria Research, Proteo-Science Center, Ehime University, Matsuyama, Ehime 790-8577, Japan. Electronic address: takashima.eizo.mz@ehime-u.ac.jp.
  • Morita M; Division of Malaria Research, Proteo-Science Center, Ehime University, Matsuyama, Ehime 790-8577, Japan. Electronic address: morita.masayuki.ls@ehime-u.ac.jp.
  • Sattabongkot J; Mahidol Vivax Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok 10400, Thailand. Electronic address: jetsumon.pra@mahidol.edu.
  • Ishino T; Division of Molecular Parasitology, Proteo-Science Center, Ehime University, Toon, Ehime 791-0295, Japan. Electronic address: tishino.vip@tmd.ac.jp.
  • Culleton R; Division of Molecular Parasitology, Proteo-Science Center, Ehime University, Toon, Ehime 791-0295, Japan. Electronic address: culleton.richard.oe@ehime-u.ac.jp.
  • Torii M; Division of Molecular Parasitology, Proteo-Science Center, Ehime University, Toon, Ehime 791-0295, Japan; Division of Malaria Research, Proteo-Science Center, Ehime University, Matsuyama, Ehime 790-8577, Japan. Electronic address: torii@m.ehime-u.ac.jp.
  • Tsuboi T; Division of Malaria Research, Proteo-Science Center, Ehime University, Matsuyama, Ehime 790-8577, Japan. Electronic address: tsuboi.takafumi.mb@ehime-u.ac.jp.
Parasitol Int ; 87: 102525, 2022 Apr.
Article em En | MEDLINE | ID: mdl-34896614
ABSTRACT
Existing control measures have significantly reduced malaria morbidity and mortality in the last two decades, although these reductions are now stalling. Significant efforts have been undertaken to develop malaria vaccines. Recently, extensive progress in malaria vaccine development has been made for Plasmodium falciparum. To date, only the RTS,S/AS01 vaccine has been tested in Phase 3 clinical trials and is now under implementation, despite modest efficacy. Therefore, the development of a malaria transmission-blocking vaccine (TBV) will be essential for malaria elimination. Only a limited number of TBVs have reached pre-clinical or clinical development with several major challenges impeding their development, including low immunogenicity in humans. TBV development efforts against P. vivax, the second major cause of malaria morbidity, lag far behind those for P. falciparum. In this review we summarize the latest progress, challenges and innovations in P. vivax TBV research and discuss how to accelerate its development.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Plasmodium vivax / Malária Vivax / Vacinas Antimaláricas Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Plasmodium vivax / Malária Vivax / Vacinas Antimaláricas Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article