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Ebola virus glycoprotein stimulates IL-18–dependent natural killer cell responses

BACKGROUND: NK cells are activated by innate cytokines and viral ligands to kill virus-infected cells. These functions are enhanced during secondary immune responses and after vaccination by synergy with effector T cells and virus-specific antibodies. In human Ebola virus infection, clinical outcome...

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Autores principales: Wagstaffe, Helen R., Clutterbuck, Elizabeth A., Bockstal, Viki, Stoop, Jeroen N., Luhn, Kerstin, Douoguih, Macaya, Shukarev, Georgi, Snape, Matthew D., Pollard, Andrew J., Riley, Eleanor M., Goodier, Martin R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Clinical Investigation 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7324188/
https://www.ncbi.nlm.nih.gov/pubmed/32315287
http://dx.doi.org/10.1172/JCI132438
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author Wagstaffe, Helen R.
Clutterbuck, Elizabeth A.
Bockstal, Viki
Stoop, Jeroen N.
Luhn, Kerstin
Douoguih, Macaya
Shukarev, Georgi
Snape, Matthew D.
Pollard, Andrew J.
Riley, Eleanor M.
Goodier, Martin R.
author_facet Wagstaffe, Helen R.
Clutterbuck, Elizabeth A.
Bockstal, Viki
Stoop, Jeroen N.
Luhn, Kerstin
Douoguih, Macaya
Shukarev, Georgi
Snape, Matthew D.
Pollard, Andrew J.
Riley, Eleanor M.
Goodier, Martin R.
author_sort Wagstaffe, Helen R.
collection PubMed
description BACKGROUND: NK cells are activated by innate cytokines and viral ligands to kill virus-infected cells. These functions are enhanced during secondary immune responses and after vaccination by synergy with effector T cells and virus-specific antibodies. In human Ebola virus infection, clinical outcome is strongly associated with the initial innate cytokine response, but the role of NK cells has not been thoroughly examined. METHODS: The novel 2-dose heterologous Adenovirus type 26.ZEBOV (Ad26.ZEBOV) and modified vaccinia Ankara-BN-Filo (MVA-BN-Filo) vaccine regimen is safe and provides specific immunity against Ebola glycoprotein, and is currently in phase 2 and 3 studies. Here, we analyzed NK cell phenotype and function in response to Ad26.ZEBOV, MVA-BN-Filo vaccination regimen and in response to in vitro Ebola glycoprotein stimulation of PBMCs isolated before and after vaccination. RESULTS: We show enhanced NK cell proliferation and activation after vaccination compared with baseline. Ebola glycoprotein–induced activation of NK cells was dependent on accessory cells and TLR-4–dependent innate cytokine secretion (predominantly from CD14(+) monocytes) and enriched within less differentiated NK cell subsets. Optimal NK cell responses were dependent on IL-18 and IL-12, whereas IFN-γ secretion was restricted by high concentrations of IL-10. CONCLUSION: This study demonstrates the induction of NK cell effector functions early after Ad26.ZEBOV, MVA-BN-Filo vaccination and provides a mechanism for the activation and regulation of NK cells by Ebola glycoprotein. TRIAL REGISTRATION: ClinicalTrials.gov NCT02313077. FUNDING: United Kingdom Medical Research Council Studentship in Vaccine Research, Innovative Medicines Initiative 2 Joint Undertaking, EBOVAC (grant 115861) and Crucell Holland (now Janssen Vaccines and Prevention B.V.), European Union’s Horizon 2020 research and innovation programme and European Federation of Pharmaceutical Industries and Associations (EFPIA).
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spelling pubmed-73241882020-07-02 Ebola virus glycoprotein stimulates IL-18–dependent natural killer cell responses Wagstaffe, Helen R. Clutterbuck, Elizabeth A. Bockstal, Viki Stoop, Jeroen N. Luhn, Kerstin Douoguih, Macaya Shukarev, Georgi Snape, Matthew D. Pollard, Andrew J. Riley, Eleanor M. Goodier, Martin R. J Clin Invest Clinical Medicine BACKGROUND: NK cells are activated by innate cytokines and viral ligands to kill virus-infected cells. These functions are enhanced during secondary immune responses and after vaccination by synergy with effector T cells and virus-specific antibodies. In human Ebola virus infection, clinical outcome is strongly associated with the initial innate cytokine response, but the role of NK cells has not been thoroughly examined. METHODS: The novel 2-dose heterologous Adenovirus type 26.ZEBOV (Ad26.ZEBOV) and modified vaccinia Ankara-BN-Filo (MVA-BN-Filo) vaccine regimen is safe and provides specific immunity against Ebola glycoprotein, and is currently in phase 2 and 3 studies. Here, we analyzed NK cell phenotype and function in response to Ad26.ZEBOV, MVA-BN-Filo vaccination regimen and in response to in vitro Ebola glycoprotein stimulation of PBMCs isolated before and after vaccination. RESULTS: We show enhanced NK cell proliferation and activation after vaccination compared with baseline. Ebola glycoprotein–induced activation of NK cells was dependent on accessory cells and TLR-4–dependent innate cytokine secretion (predominantly from CD14(+) monocytes) and enriched within less differentiated NK cell subsets. Optimal NK cell responses were dependent on IL-18 and IL-12, whereas IFN-γ secretion was restricted by high concentrations of IL-10. CONCLUSION: This study demonstrates the induction of NK cell effector functions early after Ad26.ZEBOV, MVA-BN-Filo vaccination and provides a mechanism for the activation and regulation of NK cells by Ebola glycoprotein. TRIAL REGISTRATION: ClinicalTrials.gov NCT02313077. FUNDING: United Kingdom Medical Research Council Studentship in Vaccine Research, Innovative Medicines Initiative 2 Joint Undertaking, EBOVAC (grant 115861) and Crucell Holland (now Janssen Vaccines and Prevention B.V.), European Union’s Horizon 2020 research and innovation programme and European Federation of Pharmaceutical Industries and Associations (EFPIA). American Society for Clinical Investigation 2020-06-15 2020-07-01 /pmc/articles/PMC7324188/ /pubmed/32315287 http://dx.doi.org/10.1172/JCI132438 Text en © 2020 Wagstaffe et al. http://creativecommons.org/licenses/by/4.0/ This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Clinical Medicine
Wagstaffe, Helen R.
Clutterbuck, Elizabeth A.
Bockstal, Viki
Stoop, Jeroen N.
Luhn, Kerstin
Douoguih, Macaya
Shukarev, Georgi
Snape, Matthew D.
Pollard, Andrew J.
Riley, Eleanor M.
Goodier, Martin R.
Ebola virus glycoprotein stimulates IL-18–dependent natural killer cell responses
title Ebola virus glycoprotein stimulates IL-18–dependent natural killer cell responses
title_full Ebola virus glycoprotein stimulates IL-18–dependent natural killer cell responses
title_fullStr Ebola virus glycoprotein stimulates IL-18–dependent natural killer cell responses
title_full_unstemmed Ebola virus glycoprotein stimulates IL-18–dependent natural killer cell responses
title_short Ebola virus glycoprotein stimulates IL-18–dependent natural killer cell responses
title_sort ebola virus glycoprotein stimulates il-18–dependent natural killer cell responses
topic Clinical Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7324188/
https://www.ncbi.nlm.nih.gov/pubmed/32315287
http://dx.doi.org/10.1172/JCI132438
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