Comparison of major, minor and junctional circumsporozoite protein epitopes for malaria vaccine design

Currently approved malaria vaccines (RTS,S/AS01 and R21/Matrix-M) contain the tetrapeptide major repeats (19x NPNA) and C-terminal domain of the circumsporozoite protein of Plasmodium falciparum. Incorporating the junctional (NPDP) and minor repeat (NPNV) epitope targeted by protective human monoclonal antibodies into immunogens is hypothesized to improve vaccine efficacy. However, comparisons of such candidates have yielded contradictory results due to inter-study differences. Tobacco mosaic virus (TMV) capsid virus-like particles displaying the minor repeat, junctional, and major repeat epitopes were compared in an intravenous challenge model. Despite high cross-reactivity and in vitro inhibition, minor repeat candidates did not confer sterile protection in vivo. Constructs displaying major repeats NPNAx20, NPNAx5, and a junctional+minor repeat epitope induced sterile protection. Head-to-head comparisons of selected TMV vaccines and RTS,S revealed equivalent in vivo liver burden reduction. TMV-NPNAx20 was selected for clinical-grade antigen manufacture based on its equivalent reduction in parasite burden at lower antibody concentrations.

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Publication Details

Journal
npj Vaccines
Published
2025-10-03
DOI
https://doi.org/10.1038/s41541-025-01264-0
Primary Topic
Malaria Research and Control
Type
article
Field-Weighted Citation Impact
0.00

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article

Comparison of major, minor and junctional circumsporozoite protein epitopes for malaria vaccine design

Lorraine Soisson, Shelby D. Foor, Jessica S. Bolton, Sheetij Dutta et al.
npj Vaccines
Malaria Research and Control
article

Comparison of major, minor and junctional circumsporozoite protein epitopes for malaria vaccine design

Lorraine Soisson, Shelby D. Foor, Jessica S. Bolton, Sheetij Dutta, Paul M. Robben, Gary R. Matyas, Fidel Zavala, Kutub Ashraf, Emma Ryan, Robin H. Miller, William B. Harrison, Dallas R. Brown, Alison Roth, Yevel Flores-García, Randall S. MacGill, Adrian H. Batchelor, Emily Locke, Elke S. Bergmann‐Leitner
article en

Abstract

Currently approved malaria vaccines (RTS,S/AS01 and R21/Matrix-M) contain the tetrapeptide major repeats (19x NPNA) and C-terminal domain of the circumsporozoite protein of Plasmodium falciparum. Incorporating the junctional (NPDP) and minor repeat (NPNV) epitope targeted by protective human monoclonal antibodies into immunogens is hypothesized to improve vaccine efficacy. However, comparisons of such candidates have yielded contradictory results due to inter-study differences. Tobacco mosaic virus (TMV) capsid virus-like particles displaying the minor repeat, junctional, and major repeat epitopes were compared in an intravenous challenge model. Despite high cross-reactivity and in vitro inhibition, minor repeat candidates did not confer sterile protection in vivo. Constructs displaying major repeats NPNAx20, NPNAx5, and a junctional+minor repeat epitope induced sterile protection. Head-to-head comparisons of selected TMV vaccines and RTS,S revealed equivalent in vivo liver burden reduction. TMV-NPNAx20 was selected for clinical-grade antigen manufacture based on its equivalent reduction in parasite burden at lower antibody concentrations.

npj VaccinesVol. 10(1)
Program for Appropriate Technology in Health (US), Johns Hopkins University (US), United States Agency for International Development (US), The University of Texas at Austin (US), Walter Reed Army Institute of Research (US)
U.S. Department of Defense, United States Agency for International Development, Johns Hopkins University, Congressionally Directed Medical Research Programs, Walter Reed Army Institute of Research
Openalex Percentile: Top 63%
Malaria Research and Control
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