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Immunization with GP1 but not core-like particles displaying isolated receptor-binding epitopes elicits virus-neutralizing antibodies against junín virus

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peer-reviewed

Erstveröffentlichung
2022-01-22
Authors
Roman-Sosa, Gleyder
Leske, Anne
Ficht, Xenia
Dau, Tung Huy
Holzerland, Julia
et al.
Editor
Mostafa, Ahmed
Naguib, Mahmoud M.
Wissenschaftlicher Artikel


Published in
Vaccines ; 10 (2022), 2. - Art.-Nr. 173. - eISSN 2076-393X
Link to original publication
https://dx.doi.org/10.3390/vaccines10020173
Institutions
UKU. Klinik für Innere Medizin I
Document version
published version (publisher's PDF)
Abstract
New World arenaviruses are rodent-transmitted viruses and include a number of pathogens that are responsible for causing severe human disease. This includes Junín virus (JUNV), which is the causative agent of Argentine hemorrhagic fever. The wild nature and mobility of the rodent reservoir host makes it difficult to control the disease, and currently passive immunization with high-titer neutralizing antibody-containing plasma from convalescent patients is the only specific therapy. However, dwindling supplies of naturally available convalescent plasma, and challenges in developing similar resources for other closely related viruses, have made the development of alternative antibody-based therapeutic approaches of critical importance. In this study, we sought to induce a neutralizing antibody response in rabbits against the receptor-binding subunit of the viral glycoprotein, GP1, and the specific peptide sequences in GP1 involved in cellular receptor contacts. While these specific receptor-interacting peptides did not efficiently induce the production of neutralizing antibodies when delivered as a particulate antigen (as part of hepatitis B virus core-like particles), we showed that recombinant JUNV GP1 purified from transfected mammalian cells induced virus-neutralizing antibodies at high titers in rabbits. Further, neutralization was observed across a range of unrelated JUNV strains, a feature that is critical for effectiveness in the field. These results underscore the potential of GP1 alone to induce a potent neutralizing antibody response and highlight the importance of epitope presentation. In addition, effective virus neutralization by rabbit antibodies supports the potential applicability of this species for the future development of immunotherapeutics (e.g., based on humanized monoclonal antibodies). Such information can be applied in the design of vaccines and immunogens for both prevention and specific therapies against this and likely also other closely related pathogenic New World arenaviruses.
Is supplemented by
https://www.mdpi.com/article/10.3390/vaccines10020173/s1
Subject headings
[GND]: Arenaviren | Immunreaktion | Glykoproteine
[MeSH]: Arenavirus | Immunity | Antibodies, Neutralizing | Glycoproteins
[Free subject headings]: Junín virus | immune response | glycoprotein | GP1
[DDC subject group]: DDC 610 / Medicine & health
License
CC BY 4.0 International
https://creativecommons.org/licenses/by/4.0/

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DOI & citation

Please use this identifier to cite or link to this item: http://dx.doi.org/10.18725/OPARU-50328

Roman-Sosa, Gleyder et al. (2023): Immunization with GP1 but not core-like particles displaying isolated receptor-binding epitopes elicits virus-neutralizing antibodies against junín virus. Open Access Repositorium der Universität Ulm und Technischen Hochschule Ulm. http://dx.doi.org/10.18725/OPARU-50328
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