Cargando…

Identification of Novel Malaria Transmission-Blocking Vaccine Candidates

Control measures have significantly reduced malaria morbidity and mortality in the last two decades; however, the downward trends have stalled and have become complicated by the emergence of COVID-19. Significant efforts have been made to develop malaria vaccines, but currently only the RTS,S/AS01 v...

Descripción completa

Detalles Bibliográficos
Autores principales: Takashima, Eizo, Tachibana, Mayumi, Morita, Masayuki, Nagaoka, Hikaru, Kanoi, Bernard N., Tsuboi, Takafumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8670312/
https://www.ncbi.nlm.nih.gov/pubmed/34917521
http://dx.doi.org/10.3389/fcimb.2021.805482
_version_ 1784614954031120384
author Takashima, Eizo
Tachibana, Mayumi
Morita, Masayuki
Nagaoka, Hikaru
Kanoi, Bernard N.
Tsuboi, Takafumi
author_facet Takashima, Eizo
Tachibana, Mayumi
Morita, Masayuki
Nagaoka, Hikaru
Kanoi, Bernard N.
Tsuboi, Takafumi
author_sort Takashima, Eizo
collection PubMed
description Control measures have significantly reduced malaria morbidity and mortality in the last two decades; however, the downward trends have stalled and have become complicated by the emergence of COVID-19. Significant efforts have been made to develop malaria vaccines, but currently only the RTS,S/AS01 vaccine against Plasmodium falciparum has been recommended by the WHO, for widespread use among children in sub-Saharan Africa. The efficacy of RTS,S/AS01 is modest, and therefore the development of more efficacious vaccines is still needed. In addition, the development of transmission-blocking vaccines (TBVs) to reduce the parasite transmission from humans to mosquitoes is required toward the goal of malaria elimination. Few TBVs have reached clinical development, and challenges include low immunogenicity or high reactogenicity in humans. Therefore, novel approaches to accelerate TBV research and development are urgently needed, especially novel TBV candidate discovery. In this mini review we summarize the progress in TBV research and development, novel TBV candidate discovery, and discuss how to accelerate novel TBV candidate discovery.
format Online
Article
Text
id pubmed-8670312
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-86703122021-12-15 Identification of Novel Malaria Transmission-Blocking Vaccine Candidates Takashima, Eizo Tachibana, Mayumi Morita, Masayuki Nagaoka, Hikaru Kanoi, Bernard N. Tsuboi, Takafumi Front Cell Infect Microbiol Cellular and Infection Microbiology Control measures have significantly reduced malaria morbidity and mortality in the last two decades; however, the downward trends have stalled and have become complicated by the emergence of COVID-19. Significant efforts have been made to develop malaria vaccines, but currently only the RTS,S/AS01 vaccine against Plasmodium falciparum has been recommended by the WHO, for widespread use among children in sub-Saharan Africa. The efficacy of RTS,S/AS01 is modest, and therefore the development of more efficacious vaccines is still needed. In addition, the development of transmission-blocking vaccines (TBVs) to reduce the parasite transmission from humans to mosquitoes is required toward the goal of malaria elimination. Few TBVs have reached clinical development, and challenges include low immunogenicity or high reactogenicity in humans. Therefore, novel approaches to accelerate TBV research and development are urgently needed, especially novel TBV candidate discovery. In this mini review we summarize the progress in TBV research and development, novel TBV candidate discovery, and discuss how to accelerate novel TBV candidate discovery. Frontiers Media S.A. 2021-11-30 /pmc/articles/PMC8670312/ /pubmed/34917521 http://dx.doi.org/10.3389/fcimb.2021.805482 Text en Copyright © 2021 Takashima, Tachibana, Morita, Nagaoka, Kanoi and Tsuboi https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Takashima, Eizo
Tachibana, Mayumi
Morita, Masayuki
Nagaoka, Hikaru
Kanoi, Bernard N.
Tsuboi, Takafumi
Identification of Novel Malaria Transmission-Blocking Vaccine Candidates
title Identification of Novel Malaria Transmission-Blocking Vaccine Candidates
title_full Identification of Novel Malaria Transmission-Blocking Vaccine Candidates
title_fullStr Identification of Novel Malaria Transmission-Blocking Vaccine Candidates
title_full_unstemmed Identification of Novel Malaria Transmission-Blocking Vaccine Candidates
title_short Identification of Novel Malaria Transmission-Blocking Vaccine Candidates
title_sort identification of novel malaria transmission-blocking vaccine candidates
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8670312/
https://www.ncbi.nlm.nih.gov/pubmed/34917521
http://dx.doi.org/10.3389/fcimb.2021.805482
work_keys_str_mv AT takashimaeizo identificationofnovelmalariatransmissionblockingvaccinecandidates
AT tachibanamayumi identificationofnovelmalariatransmissionblockingvaccinecandidates
AT moritamasayuki identificationofnovelmalariatransmissionblockingvaccinecandidates
AT nagaokahikaru identificationofnovelmalariatransmissionblockingvaccinecandidates
AT kanoibernardn identificationofnovelmalariatransmissionblockingvaccinecandidates
AT tsuboitakafumi identificationofnovelmalariatransmissionblockingvaccinecandidates