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Cellular and antibody response in GMZ2-vaccinated Gabonese volunteers in a controlled human malaria infection trial
BACKGROUND: Antibody and cellular memory responses following vaccination are important measures of immunogenicity. These immune markers were quantified in the framework of a vaccine trial investigating the malaria vaccine candidate GMZ2. METHODS: Fifty Gabonese adults were vaccinated with two formul...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9204906/ https://www.ncbi.nlm.nih.gov/pubmed/35715803 http://dx.doi.org/10.1186/s12936-022-04169-8 |
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author | Nouatin, Odilon Ibáñez, Javier Fendel, Rolf Ngoa, Ulysse A. Lorenz, Freia-Raphaella Dejon-Agobé, Jean-Claude Edoa, Jean Ronald Flügge, Judith Brückner, Sina Esen, Meral Theisen, Michael Hoffman, Stephen L. Moutairou, Kabirou Luty, Adrian J. F. Lell, Bertrand Kremsner, Peter G. Adegnika, Ayola A. Mordmüller, Benjamin |
author_facet | Nouatin, Odilon Ibáñez, Javier Fendel, Rolf Ngoa, Ulysse A. Lorenz, Freia-Raphaella Dejon-Agobé, Jean-Claude Edoa, Jean Ronald Flügge, Judith Brückner, Sina Esen, Meral Theisen, Michael Hoffman, Stephen L. Moutairou, Kabirou Luty, Adrian J. F. Lell, Bertrand Kremsner, Peter G. Adegnika, Ayola A. Mordmüller, Benjamin |
author_sort | Nouatin, Odilon |
collection | PubMed |
description | BACKGROUND: Antibody and cellular memory responses following vaccination are important measures of immunogenicity. These immune markers were quantified in the framework of a vaccine trial investigating the malaria vaccine candidate GMZ2. METHODS: Fifty Gabonese adults were vaccinated with two formulations (aluminum Alhydrogel and CAF01) of GMZ2 or a control vaccine (Verorab). Vaccine efficacy was assessed using controlled human malaria infection (CHMI) by direct venous inoculation of 3200 live Plasmodium falciparum sporozoites (PfSPZ Challenge). GMZ2-stimulated T and specific B-cell responses were estimated by flow cytometry before and after vaccination. Additionally, the antibody response against 212 P. falciparum antigens was estimated before CHMI by protein microarray. RESULTS: Frequencies of pro- and anti-inflammatory CD4(+) T cells stimulated with the vaccine antigen GMZ2 as well as B cell profiles did not change after vaccination. IL-10-producing CD4(+) T cells and CD20(+) IgG(+) B cells were increased post-vaccination regardless of the intervention, thus could not be specifically attributed to any malaria vaccine regimen. In contrast, GMZ2-specific antibody response increased after the vaccination, but was not correlated to protection. Antibody responses to several P. falciparum blood and liver stage antigens (MSP1, MSP4, MSP8, PfEMP1, STARP) as well as the breadth of the malaria-specific antibody response were significantly higher in protected study participants. CONCLUSIONS: In lifelong malaria exposed adults, the main marker of protection against CHMI is a broad antibody pattern recognizing multiple stages of the plasmodial life cycle. Despite vaccination with GMZ2 using a novel formulation, expansion of the GMZ2-stimulated T cells or the GMZ2-specific B cell response was limited, and the vaccine response could not be identified as a marker of protection against malaria. Trial registration PACTR; PACTR201503001038304; Registered 17 February 2015; https://pactr.samrc.ac.za/TrialDisplay.aspx?TrialID=1038 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12936-022-04169-8. |
format | Online Article Text |
id | pubmed-9204906 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-92049062022-06-18 Cellular and antibody response in GMZ2-vaccinated Gabonese volunteers in a controlled human malaria infection trial Nouatin, Odilon Ibáñez, Javier Fendel, Rolf Ngoa, Ulysse A. Lorenz, Freia-Raphaella Dejon-Agobé, Jean-Claude Edoa, Jean Ronald Flügge, Judith Brückner, Sina Esen, Meral Theisen, Michael Hoffman, Stephen L. Moutairou, Kabirou Luty, Adrian J. F. Lell, Bertrand Kremsner, Peter G. Adegnika, Ayola A. Mordmüller, Benjamin Malar J Research BACKGROUND: Antibody and cellular memory responses following vaccination are important measures of immunogenicity. These immune markers were quantified in the framework of a vaccine trial investigating the malaria vaccine candidate GMZ2. METHODS: Fifty Gabonese adults were vaccinated with two formulations (aluminum Alhydrogel and CAF01) of GMZ2 or a control vaccine (Verorab). Vaccine efficacy was assessed using controlled human malaria infection (CHMI) by direct venous inoculation of 3200 live Plasmodium falciparum sporozoites (PfSPZ Challenge). GMZ2-stimulated T and specific B-cell responses were estimated by flow cytometry before and after vaccination. Additionally, the antibody response against 212 P. falciparum antigens was estimated before CHMI by protein microarray. RESULTS: Frequencies of pro- and anti-inflammatory CD4(+) T cells stimulated with the vaccine antigen GMZ2 as well as B cell profiles did not change after vaccination. IL-10-producing CD4(+) T cells and CD20(+) IgG(+) B cells were increased post-vaccination regardless of the intervention, thus could not be specifically attributed to any malaria vaccine regimen. In contrast, GMZ2-specific antibody response increased after the vaccination, but was not correlated to protection. Antibody responses to several P. falciparum blood and liver stage antigens (MSP1, MSP4, MSP8, PfEMP1, STARP) as well as the breadth of the malaria-specific antibody response were significantly higher in protected study participants. CONCLUSIONS: In lifelong malaria exposed adults, the main marker of protection against CHMI is a broad antibody pattern recognizing multiple stages of the plasmodial life cycle. Despite vaccination with GMZ2 using a novel formulation, expansion of the GMZ2-stimulated T cells or the GMZ2-specific B cell response was limited, and the vaccine response could not be identified as a marker of protection against malaria. Trial registration PACTR; PACTR201503001038304; Registered 17 February 2015; https://pactr.samrc.ac.za/TrialDisplay.aspx?TrialID=1038 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12936-022-04169-8. BioMed Central 2022-06-17 /pmc/articles/PMC9204906/ /pubmed/35715803 http://dx.doi.org/10.1186/s12936-022-04169-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Nouatin, Odilon Ibáñez, Javier Fendel, Rolf Ngoa, Ulysse A. Lorenz, Freia-Raphaella Dejon-Agobé, Jean-Claude Edoa, Jean Ronald Flügge, Judith Brückner, Sina Esen, Meral Theisen, Michael Hoffman, Stephen L. Moutairou, Kabirou Luty, Adrian J. F. Lell, Bertrand Kremsner, Peter G. Adegnika, Ayola A. Mordmüller, Benjamin Cellular and antibody response in GMZ2-vaccinated Gabonese volunteers in a controlled human malaria infection trial |
title | Cellular and antibody response in GMZ2-vaccinated Gabonese volunteers in a controlled human malaria infection trial |
title_full | Cellular and antibody response in GMZ2-vaccinated Gabonese volunteers in a controlled human malaria infection trial |
title_fullStr | Cellular and antibody response in GMZ2-vaccinated Gabonese volunteers in a controlled human malaria infection trial |
title_full_unstemmed | Cellular and antibody response in GMZ2-vaccinated Gabonese volunteers in a controlled human malaria infection trial |
title_short | Cellular and antibody response in GMZ2-vaccinated Gabonese volunteers in a controlled human malaria infection trial |
title_sort | cellular and antibody response in gmz2-vaccinated gabonese volunteers in a controlled human malaria infection trial |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9204906/ https://www.ncbi.nlm.nih.gov/pubmed/35715803 http://dx.doi.org/10.1186/s12936-022-04169-8 |
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