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How to induce protective humoral immunity against Plasmodium falciparum circumsporozoite protein

The induction of protective humoral immune responses against sporozoite surface proteins of the human parasite Plasmodium falciparum (Pf) is a prime goal in the development of a preerythrocytic malaria vaccine. The most promising antibody target is circumsporozoite protein (CSP). Although PfCSP indu...

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Detalles Bibliográficos
Autores principales: Wahl, Ilka, Wardemann, Hedda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8754000/
https://www.ncbi.nlm.nih.gov/pubmed/35006242
http://dx.doi.org/10.1084/jem.20201313
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author Wahl, Ilka
Wardemann, Hedda
author_facet Wahl, Ilka
Wardemann, Hedda
author_sort Wahl, Ilka
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description The induction of protective humoral immune responses against sporozoite surface proteins of the human parasite Plasmodium falciparum (Pf) is a prime goal in the development of a preerythrocytic malaria vaccine. The most promising antibody target is circumsporozoite protein (CSP). Although PfCSP induces strong humoral immune responses upon vaccination, vaccine efficacy is overall limited and not durable. Here, we review recent efforts to gain a better molecular and cellular understanding of anti-PfCSP B cell responses in humans and discuss ways to overcome limitations in the induction of stable titers of high-affinity antibodies that might help to increase vaccine efficacy and promote long-lived protection.
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spelling pubmed-87540002022-01-18 How to induce protective humoral immunity against Plasmodium falciparum circumsporozoite protein Wahl, Ilka Wardemann, Hedda J Exp Med Review The induction of protective humoral immune responses against sporozoite surface proteins of the human parasite Plasmodium falciparum (Pf) is a prime goal in the development of a preerythrocytic malaria vaccine. The most promising antibody target is circumsporozoite protein (CSP). Although PfCSP induces strong humoral immune responses upon vaccination, vaccine efficacy is overall limited and not durable. Here, we review recent efforts to gain a better molecular and cellular understanding of anti-PfCSP B cell responses in humans and discuss ways to overcome limitations in the induction of stable titers of high-affinity antibodies that might help to increase vaccine efficacy and promote long-lived protection. Rockefeller University Press 2022-01-10 /pmc/articles/PMC8754000/ /pubmed/35006242 http://dx.doi.org/10.1084/jem.20201313 Text en © 2022 Wahl and Wardemann https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Wahl, Ilka
Wardemann, Hedda
How to induce protective humoral immunity against Plasmodium falciparum circumsporozoite protein
title How to induce protective humoral immunity against Plasmodium falciparum circumsporozoite protein
title_full How to induce protective humoral immunity against Plasmodium falciparum circumsporozoite protein
title_fullStr How to induce protective humoral immunity against Plasmodium falciparum circumsporozoite protein
title_full_unstemmed How to induce protective humoral immunity against Plasmodium falciparum circumsporozoite protein
title_short How to induce protective humoral immunity against Plasmodium falciparum circumsporozoite protein
title_sort how to induce protective humoral immunity against plasmodium falciparum circumsporozoite protein
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8754000/
https://www.ncbi.nlm.nih.gov/pubmed/35006242
http://dx.doi.org/10.1084/jem.20201313
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