Novel malaria antigen Plasmodium yoelii E140 induces antibody-mediated sterile protection in mice against malaria challenge

PLoS One. 2020 May 14;15(5):e0232234. doi: 10.1371/journal.pone.0232234. eCollection 2020.

Abstract

Only a small fraction of the antigens expressed by malaria parasites have been evaluated as vaccine candidates. A successful malaria subunit vaccine will likely require multiple antigenic targets to achieve broad protection with high protective efficacy. Here we describe protective efficacy of a novel antigen, Plasmodium yoelii (Py) E140 (PyE140), evaluated against P. yoelii challenge of mice. Vaccines targeting PyE140 reproducibly induced up to 100% sterile protection in both inbred and outbred murine challenge models. Although PyE140 immunization induced high frequency and multifunctional CD8+ T cell responses, as well as CD4+ T cell responses, protection was mediated by PyE140 antibodies acting against blood stage parasites. Protection in mice was long-lasting with up to 100% sterile protection at twelve weeks post-immunization and durable high titer anti-PyE140 antibodies. The E140 antigen is expressed in all Plasmodium species, is highly conserved in both P. falciparum lab-adapted strains and endemic circulating parasites, and is thus a promising lead vaccine candidate for future evaluation against human malaria parasite species.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Antibodies, Protozoan / immunology*
  • Antigens, Protozoan / genetics
  • Antigens, Protozoan / immunology*
  • Cross Reactions
  • Female
  • Gene Expression Regulation
  • Immunization*
  • Malaria / prevention & control*
  • Mice
  • Plasmodium yoelii / genetics
  • Plasmodium yoelii / immunology
  • Plasmodium yoelii / physiology*

Substances

  • Antibodies, Protozoan
  • Antigens, Protozoan

Grants and funding

EV received support for this study from Military Infectious Diseases Research Program (MIDRP) Proposals F0339_13_NM and F0482_16_NM, funding work unit number A1217; MS received support for this study from MIDRP Proposals F0409_14_WR_CS and F0523_17_WR_CS, funding work unit number A1256. MIDRP provided support in the form of salaries for authors (EV, MS, and KG) and in the form of contract support for CAMRIS International (NR, KO, JW, and JCA), Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc. (HJF) (ECS, KJL, JSB, MD, SS, RV, AB, RD, JML, NBP, and MRH), and University of Maryland (JBS). The United States Agency for International Development (USAID) provided support to NMRC through an interagency agreement, number AID-GH-T-17-00002, received by EV, for an NMRC contract with HJF (JKM). This material is based upon work supported by the Naval Medical Research Center - Silver Spring, MD, under contract N6264518C4003. Any opinions, findings and conclusions or recommendations expressed in this material are those of the author(s) and do not necessarily reflect the views of the Naval Medical Research Center and the Naval Medical Logistics Command. The funders (MIDRP and USAID) did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of each author are articulated in the ‘author contributions’ section.