4.6 Article

A guide to investigating immune responses elicited by whole-sporozoite pre-erythrocytic vaccines against malaria

Journal

FEBS JOURNAL
Volume 289, Issue 12, Pages 3335-3359

Publisher

WILEY
DOI: 10.1111/febs.16016

Keywords

antibodies; cellular responses; controlled human malaria infection; humoral responses; immunity; liver; lymphocytes; P; falciparum; Plasmodium; vaccination

Funding

  1. FundacAo para a Ciencia e Tecnologia [CEECIND/03539/2017, PTDC-SAU-INF-29550-2017]
  2. Fundação para a Ciência e a Tecnologia [PTDC/SAU-INF/29550/2017] Funding Source: FCT

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Efforts have been made to develop efficient vaccines against malaria, with Whole-sporozoite (Wsp) vaccines showing promise in inducing immune responses against Plasmodium parasites. Various approaches for Wsp PE vaccination are currently under evaluation, with clinical trials focusing on assessing protective efficacy and investigating immune responses.
In the last few decades, considerable efforts have been made toward the development of efficient vaccines against malaria. Whole-sporozoite (Wsp) vaccines, which induce efficient immune responses against the pre-erythrocytic (PE) stages (sporozoites and liver forms) of Plasmodium parasites, the causative agents of malaria, are among the most promising immunization strategies tested until present. Several Wsp PE vaccination approaches are currently under evaluation in the clinic, including radiation- or genetically-attenuated Plasmodium sporozoites, live parasites combined with chemoprophylaxis, or genetically modified rodent Plasmodium parasites. In addition to the assessment of their protective efficacy, clinical trials of Wsp PE vaccine candidates inevitably involve the thorough investigation of the immune responses elicited by vaccination, as well as the identification of correlates of protection. Here, we review the main methodologies employed to dissect the humoral and cellular immune responses observed in the context of Wsp PE vaccine clinical trials and discuss future strategies to further deepen the knowledge generated by these studies, providing a toolbox for the in-depth analysis of vaccine-induced immunogenicity.

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