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Review
. 2022 Jun;289(12):3335-3359.
doi: 10.1111/febs.16016. Epub 2021 Jun 1.

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

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Free article
Review

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

Diana Moita et al. FEBS J. 2022 Jun.
Free article

Abstract

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.

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

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References

    1. World Health Organization (2020). World Malaria Report 2020. https://www.who.int/publications/i/item/9789240015791
    1. Bhatt S, Weiss DJ, Cameron E, Bisanzio D, Mappin B, Dalrymple U, Battle KE, Moyes CL, Henry A, Eckhoff PA et al. (2015) The effect of malaria control on Plasmodium falciparum in Africa between 2000 and 2015. Nature 526, 207-211.
    1. Dhiman S (2019) Are malaria elimination efforts on right track? An analysis of gains achieved and challenges ahead. Infect Dis Poverty 8, 1-19.
    1. Langhorne J, Ndungu FM, Sponaas AM & Marsh K (2008) Immunity to malaria: more questions than answers. Nat Immunol 9, 725-732.
    1. Crompton PD, Pierce SK & Miller LH (2010) Advances and challenges in malaria vaccine development. J Clin Invest 120, 4168-4178.

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