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Immune response to a conserved enteroviral epitope of the major capsid VP1 protein is associated with lower risk of cardiovascular disease
BACKGROUND: Major cardiac events including myocardial infarction (MI) are associated with viral infections. However, how specific infections contribute to the cardiovascular insults has remained largely unclear. METHODS: We employed next generation phage display mimotope-variation analysis (MVA) to...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8801986/ https://www.ncbi.nlm.nih.gov/pubmed/35091341 http://dx.doi.org/10.1016/j.ebiom.2022.103835 |
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author | Pupina, Nadežda Avarlaid, Annela Sadam, Helle Pihlak, Arno Jaago, Mariliis Tuvikene, Jürgen Rähni, Annika Planken, Anu Planken, Margus Kalso, Eija Tienari, Pentti J. Nieminen, Janne K. Seppänen, Mikko R.J. Vaheri, Antti Lindholm, Dan Sinisalo, Juha Pussinen, Pirkko Timmusk, Tõnis Palm, Kaia |
author_facet | Pupina, Nadežda Avarlaid, Annela Sadam, Helle Pihlak, Arno Jaago, Mariliis Tuvikene, Jürgen Rähni, Annika Planken, Anu Planken, Margus Kalso, Eija Tienari, Pentti J. Nieminen, Janne K. Seppänen, Mikko R.J. Vaheri, Antti Lindholm, Dan Sinisalo, Juha Pussinen, Pirkko Timmusk, Tõnis Palm, Kaia |
author_sort | Pupina, Nadežda |
collection | PubMed |
description | BACKGROUND: Major cardiac events including myocardial infarction (MI) are associated with viral infections. However, how specific infections contribute to the cardiovascular insults has remained largely unclear. METHODS: We employed next generation phage display mimotope-variation analysis (MVA) to explore the link between antibody-based immune response and severe cardiovascular conditions. Here, we used a case-control design, including the first-stage discovery cohort (n = 100), along with cohorts for second-stage discovery (n = 329) and validation (n = 466). FINDINGS: We observed strong antibody response to the peptide antigens with Gly-Ile-X-Asp (G-I-X-D) core structure in healthy individuals but not in patients with MI. Analysis of the origin of this epitope linked it with the N-terminus of the VP1 protein of poliovirus 3 (PV3), but also other species of picornaviruses. Consistently, we found low levels of antibody response to the G-I-X-D epitope in individuals with severe cardiac disease complications. INTERPRETATION: Our findings imply that antibody response to the G-I-X-D epitope is associated with polio vaccinations and that high antibody levels to this epitope could discriminate healthy individuals from prospective MI patients as a blood-derived biomarker. Together, these findings highlight the importance of epitope-specific antibody response and suggest that protective immunity against the polio- and non-polio enteroviral infections support improved cardiovascular health. FUNDING: Estonian Ministry of Education (5.1-4/20/170), Estonian Research Council (PRG573, PRG805), H2020-MSCA-RISE-2016 (EU734791), H2020 PANBioRA (EU760921), European Union through the European Regional Development Fund (Project no. 2014-2020.4.01.15-0012), Helsinki University Hospital grants, Mary and Georg C. Ehrnrooth Foundation, Finnish Eye Foundation, Finska Läkaresällskapet, The Finnish Society of Sciences and Letters, Magnus Ehrnrooth Foundation and Sigrid Jusélius Foundation. |
format | Online Article Text |
id | pubmed-8801986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-88019862022-02-09 Immune response to a conserved enteroviral epitope of the major capsid VP1 protein is associated with lower risk of cardiovascular disease Pupina, Nadežda Avarlaid, Annela Sadam, Helle Pihlak, Arno Jaago, Mariliis Tuvikene, Jürgen Rähni, Annika Planken, Anu Planken, Margus Kalso, Eija Tienari, Pentti J. Nieminen, Janne K. Seppänen, Mikko R.J. Vaheri, Antti Lindholm, Dan Sinisalo, Juha Pussinen, Pirkko Timmusk, Tõnis Palm, Kaia EBioMedicine Articles BACKGROUND: Major cardiac events including myocardial infarction (MI) are associated with viral infections. However, how specific infections contribute to the cardiovascular insults has remained largely unclear. METHODS: We employed next generation phage display mimotope-variation analysis (MVA) to explore the link between antibody-based immune response and severe cardiovascular conditions. Here, we used a case-control design, including the first-stage discovery cohort (n = 100), along with cohorts for second-stage discovery (n = 329) and validation (n = 466). FINDINGS: We observed strong antibody response to the peptide antigens with Gly-Ile-X-Asp (G-I-X-D) core structure in healthy individuals but not in patients with MI. Analysis of the origin of this epitope linked it with the N-terminus of the VP1 protein of poliovirus 3 (PV3), but also other species of picornaviruses. Consistently, we found low levels of antibody response to the G-I-X-D epitope in individuals with severe cardiac disease complications. INTERPRETATION: Our findings imply that antibody response to the G-I-X-D epitope is associated with polio vaccinations and that high antibody levels to this epitope could discriminate healthy individuals from prospective MI patients as a blood-derived biomarker. Together, these findings highlight the importance of epitope-specific antibody response and suggest that protective immunity against the polio- and non-polio enteroviral infections support improved cardiovascular health. FUNDING: Estonian Ministry of Education (5.1-4/20/170), Estonian Research Council (PRG573, PRG805), H2020-MSCA-RISE-2016 (EU734791), H2020 PANBioRA (EU760921), European Union through the European Regional Development Fund (Project no. 2014-2020.4.01.15-0012), Helsinki University Hospital grants, Mary and Georg C. Ehrnrooth Foundation, Finnish Eye Foundation, Finska Läkaresällskapet, The Finnish Society of Sciences and Letters, Magnus Ehrnrooth Foundation and Sigrid Jusélius Foundation. Elsevier 2022-01-25 /pmc/articles/PMC8801986/ /pubmed/35091341 http://dx.doi.org/10.1016/j.ebiom.2022.103835 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Articles Pupina, Nadežda Avarlaid, Annela Sadam, Helle Pihlak, Arno Jaago, Mariliis Tuvikene, Jürgen Rähni, Annika Planken, Anu Planken, Margus Kalso, Eija Tienari, Pentti J. Nieminen, Janne K. Seppänen, Mikko R.J. Vaheri, Antti Lindholm, Dan Sinisalo, Juha Pussinen, Pirkko Timmusk, Tõnis Palm, Kaia Immune response to a conserved enteroviral epitope of the major capsid VP1 protein is associated with lower risk of cardiovascular disease |
title | Immune response to a conserved enteroviral epitope of the major capsid VP1 protein is associated with lower risk of cardiovascular disease |
title_full | Immune response to a conserved enteroviral epitope of the major capsid VP1 protein is associated with lower risk of cardiovascular disease |
title_fullStr | Immune response to a conserved enteroviral epitope of the major capsid VP1 protein is associated with lower risk of cardiovascular disease |
title_full_unstemmed | Immune response to a conserved enteroviral epitope of the major capsid VP1 protein is associated with lower risk of cardiovascular disease |
title_short | Immune response to a conserved enteroviral epitope of the major capsid VP1 protein is associated with lower risk of cardiovascular disease |
title_sort | immune response to a conserved enteroviral epitope of the major capsid vp1 protein is associated with lower risk of cardiovascular disease |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8801986/ https://www.ncbi.nlm.nih.gov/pubmed/35091341 http://dx.doi.org/10.1016/j.ebiom.2022.103835 |
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