TY - JOUR
T1 - The mRNA Vaccine Technology Era and the Future Control of Parasitic Infections
AU - You, Hong
AU - Jones, Malcolm K.
AU - Gordon, Catherine A.
AU - Arganda, Alexa E.
AU - Cai, Pengfei
AU - Al-Wassiti, Harry
AU - Pouton, Colin W.
AU - McManus, Donald P.
N1 - Funding Information:
Our studies on schistosomiasis and other NTDs received support from an NHMRC (National Health and Medical Research Council) of Australia Investigator Grant to D.P.M. (APP1194462) and QIMR Berghofer Medical Research Institute seed grants (2021 and 2022) to H.Y. C.W.P. and H.A.-W. acknowledge financial research support from the NHMRC, Medical Research Future Fund (MRFF), mRNA Victoria, and Monash University for their mRNA research. We declare that we have no conflicts of interest.
Publisher Copyright:
© 2023 American Society for Microbiology. All Rights Reserved.
PY - 2023/3
Y1 - 2023/3
N2 - Despite intensive long-term efforts, with very few exceptions, the development of effective vaccines against parasitic infections has presented considerable challenges, given the complexity of parasite life cycles, the interplay between parasites and their hosts, and their capacity to escape the host immune system and to regulate host immune responses. For many parasitic diseases, conventional vaccine platforms have generally proven ill suited, considering the complex manufacturing processes involved and the costs they incur, the inability to posttranslationally modify cloned target antigens, and the absence of long-lasting protective immunity induced by these antigens. An effective antiparasite vaccine platform is required to assess the effectiveness of novel vaccine candidates at high throughput. By exploiting the approach that has recently been used successfully to produce highly protective COVID mRNA vaccines, we anticipate a new wave of research to advance the use of mRNA vaccines to prevent parasitic infections in the near future. This article considers the characteristics that are required to develop a potent antiparasite vaccine and provides a conceptual foundation to promote the development of parasite mRNA-based vaccines. We review the recent advances and challenges encountered in developing antiparasite vaccines and evaluate the potential of developing mRNA vaccines against parasites, including those causing diseases such as malaria and schistosomiasis, against which vaccines are currently suboptimal or not yet available.
AB - Despite intensive long-term efforts, with very few exceptions, the development of effective vaccines against parasitic infections has presented considerable challenges, given the complexity of parasite life cycles, the interplay between parasites and their hosts, and their capacity to escape the host immune system and to regulate host immune responses. For many parasitic diseases, conventional vaccine platforms have generally proven ill suited, considering the complex manufacturing processes involved and the costs they incur, the inability to posttranslationally modify cloned target antigens, and the absence of long-lasting protective immunity induced by these antigens. An effective antiparasite vaccine platform is required to assess the effectiveness of novel vaccine candidates at high throughput. By exploiting the approach that has recently been used successfully to produce highly protective COVID mRNA vaccines, we anticipate a new wave of research to advance the use of mRNA vaccines to prevent parasitic infections in the near future. This article considers the characteristics that are required to develop a potent antiparasite vaccine and provides a conceptual foundation to promote the development of parasite mRNA-based vaccines. We review the recent advances and challenges encountered in developing antiparasite vaccines and evaluate the potential of developing mRNA vaccines against parasites, including those causing diseases such as malaria and schistosomiasis, against which vaccines are currently suboptimal or not yet available.
KW - antiparasite vaccines
KW - malaria
KW - mRNA vaccine
KW - parasitic infections
KW - schistosomiasis
UR - http://www.scopus.com/inward/record.url?scp=85151043440&partnerID=8YFLogxK
U2 - 10.1128/cmr.00241-21
DO - 10.1128/cmr.00241-21
M3 - Review Article
C2 - 36625671
AN - SCOPUS:85151043440
SN - 0893-8512
VL - 36
SP - 1
EP - 28
JO - Clinical Microbiology Reviews
JF - Clinical Microbiology Reviews
IS - 1
ER -