| Literature DB >> 32451496 |
Rajagopal Murugan1, Stephen W Scally2,3, Giulia Costa4, Ghulam Mustafa1, Elaine Thai2,5, Tizian Decker1, Alexandre Bosch2, Katherine Prieto2, Elena A Levashina6, Jean-Philippe Julien7,8,9, Hedda Wardemann10.
Abstract
The circumsporozoite protein of the human malaria parasite Plasmodium falciparum (PfCSP) is the main target of antibodies that prevent the infection and disease, as shown in animal models. However, the limited efficacy of the PfCSP-based vaccine RTS,S calls for a better understanding of the mechanisms driving the development of the most potent human PfCSP antibodies and identification of their target epitopes. By characterizing 200 human monoclonal PfCSP antibodies induced by sporozoite immunization, we establish that the most potent antibodies bind around a conserved (N/D)PNANPN(V/A) core. High antibody affinity to the core correlates with protection from parasitemia in mice and evolves around the recognition of NANP motifs. The data suggest that the rational design of a next-generation PfCSP vaccine that elicits high-affinity antibody responses against the core epitope will promote the induction of protective humoral immune responses.Entities:
Year: 2020 PMID: 32451496 DOI: 10.1038/s41591-020-0881-9
Source DB: PubMed Journal: Nat Med ISSN: 1078-8956 Impact factor: 53.440