Complement in malaria immunity and vaccines

Developing efficacious vaccines for human malaria caused by Plasmodium falciparum is a major global health priority, although this has proven to be immensely challenging over the decades. One major hindrance is the incomplete understanding of specific immune responses that confer protection against...

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Veröffentlicht in:Immunological reviews 2020-01, Vol.293 (1), p.38-56
Hauptverfasser: Kurtovic, Liriye, Boyle, Michelle J., Opi, D. Herbert, Kennedy, Alexander T., Tham, Wai‐Hong, Reiling, Linda, Chan, Jo‐Anne, Beeson, James G.
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container_end_page 56
container_issue 1
container_start_page 38
container_title Immunological reviews
container_volume 293
creator Kurtovic, Liriye
Boyle, Michelle J.
Opi, D. Herbert
Kennedy, Alexander T.
Tham, Wai‐Hong
Reiling, Linda
Chan, Jo‐Anne
Beeson, James G.
description Developing efficacious vaccines for human malaria caused by Plasmodium falciparum is a major global health priority, although this has proven to be immensely challenging over the decades. One major hindrance is the incomplete understanding of specific immune responses that confer protection against disease and/or infection. While antibodies to play a crucial role in malaria immunity, the functional mechanisms of these antibodies remain unclear as most research has primarily focused on the direct inhibitory or neutralizing activity of antibodies. Recently, there is a growing body of evidence that antibodies can also mediate effector functions through activating the complement system against multiple developmental stages of the parasite life cycle. These antibody‐complement interactions can have detrimental consequences to parasite function and viability, and have been significantly associated with protection against clinical malaria in naturally acquired immunity, and emerging findings suggest these mechanisms could contribute to vaccine‐induced immunity. In order to develop highly efficacious vaccines, strategies are needed that prioritize the induction of antibodies with enhanced functional activity, including the ability to activate complement. Here we review the role of complement in acquired immunity to malaria, and provide insights into how this knowledge could be used to harness complement in malaria vaccine development.
doi_str_mv 10.1111/imr.12802
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Recently, there is a growing body of evidence that antibodies can also mediate effector functions through activating the complement system against multiple developmental stages of the parasite life cycle. These antibody‐complement interactions can have detrimental consequences to parasite function and viability, and have been significantly associated with protection against clinical malaria in naturally acquired immunity, and emerging findings suggest these mechanisms could contribute to vaccine‐induced immunity. In order to develop highly efficacious vaccines, strategies are needed that prioritize the induction of antibodies with enhanced functional activity, including the ability to activate complement. 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subjects Animals
Antibodies
Antibodies, Protozoan - immunology
Complement
Complement activation
Complement Activation - immunology
Complement System Proteins - immunology
Developmental stages
Disease Models, Animal
Erythrocytes - immunology
Erythrocytes - metabolism
Erythrocytes - parasitology
Global health
Host-Parasite Interactions - immunology
Humans
Immune response
Immunity
Immunity, Innate
Immunization, Passive
Immunoglobulins
Invited Review
Invited Reviews
Life cycles
Malaria
Malaria Vaccines - administration & dosage
Malaria Vaccines - immunology
Malaria, Falciparum - immunology
Malaria, Falciparum - prevention & control
Parasites
Plasmodium falciparum
Plasmodium falciparum - growth & development
Plasmodium falciparum - immunology
Vaccine development
Vaccines
Vector-borne diseases
Viability
title Complement in malaria immunity and vaccines
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