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The challenges of Plasmodium vivax human malaria infection models for vaccine development
Wanlapa Roobsoong1, Anjali Yadava2, Simon J Draper3
1Mahidol Vivax Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Abstract:
Controlled Human Malaria Infection models (CHMI) have been critical to advancing new vaccines for malaria. Stringent and safe preparation of a challenge agent is key to the success of any CHMI. Difficulty producing the Plasmodium vivax parasite in vitro has limited production of qualified parasites for CHMI as well as the functional assays required to screen and down-select candidate vaccines for this globally distributed parasite. This and other challenges to P. vivax CHMI (PvCHMI), including scientific, logistical, and ethical obstacles, are common to P. vivax research conducted in both non-endemic and endemic countries, with additional hurdles unique to each. The challenges of using CHMI for P. vivax vaccine development and evaluation, lessons learned from previous and ongoing clinical trials, and the way forward to effectively perform PvCHMI to support vaccine development, are discussed.
Insights
Controlled Human Malaria Infection (CHMI) models are vital for malaria vaccine development. Challenges in producing Plasmodium vivax parasites in vitro and other obstacles hinder effective P. vivax CHMI and vaccine advancement.
Area of Science:
- Tropical Medicine and Infectious Diseases
- Vaccinology
- Parasitology
Background:
- Controlled Human Malaria Infection (CHMI) models are essential for developing new malaria vaccines.
- Plasmodium vivax malaria poses unique challenges due to difficulties in in vitro parasite cultivation.
- Limited availability of qualified P. vivax parasites restricts CHMI efficacy and vaccine screening.
Purpose of the Study:
- To discuss the challenges associated with P. vivax CHMI for vaccine development.
- To review lessons learned from past and ongoing clinical trials.
- To propose a way forward for effective P. vivax CHMI to support vaccine advancement.
Main Methods:
- Review of scientific, logistical, and ethical obstacles in P. vivax research.
- Analysis of challenges in P. vivax parasite production for CHMI.
- Evaluation of lessons learned from P. vivax CHMI clinical trials.
Main Results:
- Difficulty in in vitro P. vivax culture significantly limits parasite production for CHMI.
- Numerous scientific, logistical, and ethical hurdles impede P. vivax CHMI.
- Both endemic and non-endemic settings face distinct challenges in P. vivax research.
Conclusions:
- Overcoming P. vivax cultivation and CHMI challenges is critical for vaccine development.
- Addressing scientific, logistical, and ethical barriers is necessary for progress.
- Strategic approaches are needed to enable effective P. vivax CHMI and accelerate vaccine candidates.
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