Monoclonal antibodies to the circumsporozoite proteins as an emerging tool for malaria prevention
Despite various public health strategies, malaria caused by Plasmodium falciparum parasites remains a major global health challenge that requires development of new interventions. Extended half-life human monoclonal antibodies targeting the P. falciparum circumsporozoite protein on sporozoites, the...
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Veröffentlicht in: | Nature immunology 2024-09, Vol.25 (9), p.1530-1545 |
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Sprache: | eng |
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Zusammenfassung: | Despite various public health strategies, malaria caused by
Plasmodium falciparum
parasites remains a major global health challenge that requires development of new interventions. Extended half-life human monoclonal antibodies targeting the
P. falciparum
circumsporozoite protein on sporozoites, the infective form of malaria parasites, prevent malaria in rodents and humans and have been advanced into clinical development. The protective epitopes on the circumsporozoite protein targeted by monoclonal antibodies have been defined. Cryogenic electron and multiphoton microscopy have enabled mechanistic structural and functional investigations of how antibodies bind to the circumsporozoite protein and neutralize sporozoites. Moreover, innovations in bioinformatics and antibody engineering have facilitated enhancement of antibody potency and durability. Here, we summarize the latest scientific advances in understanding how monoclonal antibodies to the circumsporozoite protein prevent malaria and highlight existing clinical data and future plans for how this emerging intervention can be used alone or alongside existing antimalarial interventions to control malaria across at-risk populations.
Seder and colleagues review the latest scientific advances in understanding how monoclonal antibodies to the circumsporozoite protein prevent malaria and highlight how this emerging intervention can be used alone or alongside existing antimalarial interventions to control malaria across at-risk populations. |
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ISSN: | 1529-2908 1529-2916 1529-2916 |
DOI: | 10.1038/s41590-024-01938-2 |