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Likelihood of prior exposure to circulating influenza viruses resulting in cross‐protection by CD8+ T cells against emergent H3N2v swine viruses infecting humans
Outbreaks of influenza in swine can result in potential threats to human public health. A notable occurrence was the emergence of swine‐origin H1N1 influenza viruses in 2009. Since then, there have been several documented outbreaks of swine‐origin influenza infecting humans in several countries. Sus...
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Published in: | Journal of medical virology 2022-02, Vol.94 (2), p.567-574 |
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description | Outbreaks of influenza in swine can result in potential threats to human public health. A notable occurrence was the emergence of swine‐origin H1N1 influenza viruses in 2009. Since then, there have been several documented outbreaks of swine‐origin influenza infecting humans in several countries. Sustained events have occurred when H1N1v, H1N2v, and H3N2v swine‐origin viruses have infected humans visiting agricultural shows in the US. The predominant H3N2v viruses gained the matrix protein from the A(H1N1)pdm09 viruses, with reported human‐to‐human transmission raising fears of another pandemic. Current vaccines do not induce secondary cell‐mediated immune responses, which may provide cross‐protection against novel influenza A subtypes, however, population susceptibility to infection with seasonal influenza is likely to be influenced by cross‐reactive CD8+ T‐cells directed towards immunogenic peptides derived from viral proteins. This study involved a retrospective review of historical influenza viruses circulating in human populations from 1918 to 2020 to identify evidence of prior circulation of H3N3v immunogenic CD8+ T‐cells peptides found in the NP and M1 proteins. We found evidence of prior circulation of H3N2v NP and M1 immunogenic peptides in historical influenza viruses. This provides insight into the population context in which influenza viruses emerge and may help inform immunogenic peptide selection for cytotoxic T‐cell lymphocytes (CTL)‐inducing influenza vaccines. Next‐generation vaccines capable of eliciting CD8+ T‐cell‐mediated cross‐protective immunity may offer a long‐term alternative strategy for influenza vaccines.
Highlights
Swine origin influenza viruses remain a continuing threat to human health.
Current influenza vaccines do not provide protection against novel influenza viruses.
CD8+ Tcell immunogenic peptides in the NP and M1 proteins of the H3N2v influenza viruses were investigated for evidence of prior circulation in human influenza viruses.
Vaccines based on common CD8+ Tcell immunogenic peptides may be able to mimic cross protection provided by influenza infection. |
doi_str_mv | 10.1002/jmv.27299 |
format | article |
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Highlights
Swine origin influenza viruses remain a continuing threat to human health.
Current influenza vaccines do not provide protection against novel influenza viruses.
CD8+ Tcell immunogenic peptides in the NP and M1 proteins of the H3N2v influenza viruses were investigated for evidence of prior circulation in human influenza viruses.
Vaccines based on common CD8+ Tcell immunogenic peptides may be able to mimic cross protection provided by influenza infection.</description><identifier>ISSN: 0146-6615</identifier><identifier>EISSN: 1096-9071</identifier><identifier>DOI: 10.1002/jmv.27299</identifier><identifier>PMID: 34449904</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Adolescent ; Adult ; Aged ; Animals ; B-Lymphocytes - immunology ; CD8 antigen ; CD8-Positive T-Lymphocytes - immunology ; Child ; Child, Preschool ; Cross Protection ; Cytotoxicity ; Disease Outbreaks ; Female ; H3N2v ; Health risks ; Human populations ; Humans ; immunogenic ; Immunogenicity ; Infant ; Infections ; Influenza ; Influenza A ; Influenza A Virus, H3N2 Subtype - genetics ; Influenza A Virus, H3N2 Subtype - immunology ; Influenza, Human - immunology ; Influenza, Human - virology ; Lymphocytes ; Lymphocytes T ; Male ; Matrix protein ; Middle Aged ; Orthomyxoviridae ; Orthomyxoviridae Infections - immunology ; Orthomyxoviridae Infections - virology ; Outbreaks ; Pandemics ; Peptides ; Proteins ; Public health ; Retrospective Studies ; Swine ; Swine flu ; T-Lymphocytes, Cytotoxic - immunology ; Vaccines ; Virology ; Viruses ; Young Adult</subject><ispartof>Journal of medical virology, 2022-02, Vol.94 (2), p.567-574</ispartof><rights>2021 Wiley Periodicals LLC</rights><rights>2021 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3889-e864d1fc8809087ef700ff775c37a70b9a658dd164d5389ed7bc3cc7e8e1a14c3</citedby><cites>FETCH-LOGICAL-c3889-e864d1fc8809087ef700ff775c37a70b9a658dd164d5389ed7bc3cc7e8e1a14c3</cites><orcidid>0000-0002-8751-5730</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34449904$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Komadina, Naomi</creatorcontrib><creatorcontrib>Sullivan, Sheena G.</creatorcontrib><creatorcontrib>Leder, Karin</creatorcontrib><creatorcontrib>McVernon, Jodie</creatorcontrib><title>Likelihood of prior exposure to circulating influenza viruses resulting in cross‐protection by CD8+ T cells against emergent H3N2v swine viruses infecting humans</title><title>Journal of medical virology</title><addtitle>J Med Virol</addtitle><description>Outbreaks of influenza in swine can result in potential threats to human public health. A notable occurrence was the emergence of swine‐origin H1N1 influenza viruses in 2009. Since then, there have been several documented outbreaks of swine‐origin influenza infecting humans in several countries. Sustained events have occurred when H1N1v, H1N2v, and H3N2v swine‐origin viruses have infected humans visiting agricultural shows in the US. The predominant H3N2v viruses gained the matrix protein from the A(H1N1)pdm09 viruses, with reported human‐to‐human transmission raising fears of another pandemic. Current vaccines do not induce secondary cell‐mediated immune responses, which may provide cross‐protection against novel influenza A subtypes, however, population susceptibility to infection with seasonal influenza is likely to be influenced by cross‐reactive CD8+ T‐cells directed towards immunogenic peptides derived from viral proteins. This study involved a retrospective review of historical influenza viruses circulating in human populations from 1918 to 2020 to identify evidence of prior circulation of H3N3v immunogenic CD8+ T‐cells peptides found in the NP and M1 proteins. We found evidence of prior circulation of H3N2v NP and M1 immunogenic peptides in historical influenza viruses. This provides insight into the population context in which influenza viruses emerge and may help inform immunogenic peptide selection for cytotoxic T‐cell lymphocytes (CTL)‐inducing influenza vaccines. Next‐generation vaccines capable of eliciting CD8+ T‐cell‐mediated cross‐protective immunity may offer a long‐term alternative strategy for influenza vaccines.
Highlights
Swine origin influenza viruses remain a continuing threat to human health.
Current influenza vaccines do not provide protection against novel influenza viruses.
CD8+ Tcell immunogenic peptides in the NP and M1 proteins of the H3N2v influenza viruses were investigated for evidence of prior circulation in human influenza viruses.
Vaccines based on common CD8+ Tcell immunogenic peptides may be able to mimic cross protection provided by influenza infection.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Animals</subject><subject>B-Lymphocytes - immunology</subject><subject>CD8 antigen</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cross Protection</subject><subject>Cytotoxicity</subject><subject>Disease Outbreaks</subject><subject>Female</subject><subject>H3N2v</subject><subject>Health risks</subject><subject>Human populations</subject><subject>Humans</subject><subject>immunogenic</subject><subject>Immunogenicity</subject><subject>Infant</subject><subject>Infections</subject><subject>Influenza</subject><subject>Influenza A</subject><subject>Influenza A Virus, H3N2 Subtype - genetics</subject><subject>Influenza A Virus, H3N2 Subtype - immunology</subject><subject>Influenza, Human - immunology</subject><subject>Influenza, Human - virology</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Male</subject><subject>Matrix protein</subject><subject>Middle Aged</subject><subject>Orthomyxoviridae</subject><subject>Orthomyxoviridae Infections - immunology</subject><subject>Orthomyxoviridae Infections - virology</subject><subject>Outbreaks</subject><subject>Pandemics</subject><subject>Peptides</subject><subject>Proteins</subject><subject>Public health</subject><subject>Retrospective Studies</subject><subject>Swine</subject><subject>Swine flu</subject><subject>T-Lymphocytes, Cytotoxic - immunology</subject><subject>Vaccines</subject><subject>Virology</subject><subject>Viruses</subject><subject>Young Adult</subject><issn>0146-6615</issn><issn>1096-9071</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp1kc9uEzEQhy0EomnhwAsgS1yoqm3H-8_2EQVoQQEuhevK8c6mDrt2aq9TwolH4B14sz5JnSb0gMTJh_nm88z8CHnB4JQB5GfLYX2a81zKR2TCQNaZBM4ekwmwss7qmlUH5DCEJQAImedPyUFRlqWUUE7In5n5jr25cq6lrqMrb5yn-GPlQvRIR0e18Tr2ajR2QY3t-oj2p6Jr42PAQD2G2O9rVHsXwu2v3yvvRtSjcZbON3T6VpzQS6qx7wNVC2VsGCkO6BdoR3pRfM7XNNwYiw_S9M22PUmv4qBseEaedKoP-Hz_HpGv799dTi-y2ZfzD9M3s0wXQsgMRV22rNNCgATBseMAXcd5pQuuOMylqivRtixRVSEktnyuC605CmSKlbo4Iq933rTAdcQwNoMJ27mVRRdDk1d1DYVgnCf01T_o0kVv03RNXoMAtmUTdbyj7i_jsWvSfQflNw2DZptck5Jr7pNL7Mu9Mc4HbB_Iv1El4GwH3JgeN_83NR8_fdsp7wDa-aaE</recordid><startdate>202202</startdate><enddate>202202</enddate><creator>Komadina, Naomi</creator><creator>Sullivan, Sheena G.</creator><creator>Leder, Karin</creator><creator>McVernon, Jodie</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8751-5730</orcidid></search><sort><creationdate>202202</creationdate><title>Likelihood of prior exposure to circulating influenza viruses resulting in cross‐protection by CD8+ T cells against emergent H3N2v swine viruses infecting humans</title><author>Komadina, Naomi ; 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A notable occurrence was the emergence of swine‐origin H1N1 influenza viruses in 2009. Since then, there have been several documented outbreaks of swine‐origin influenza infecting humans in several countries. Sustained events have occurred when H1N1v, H1N2v, and H3N2v swine‐origin viruses have infected humans visiting agricultural shows in the US. The predominant H3N2v viruses gained the matrix protein from the A(H1N1)pdm09 viruses, with reported human‐to‐human transmission raising fears of another pandemic. Current vaccines do not induce secondary cell‐mediated immune responses, which may provide cross‐protection against novel influenza A subtypes, however, population susceptibility to infection with seasonal influenza is likely to be influenced by cross‐reactive CD8+ T‐cells directed towards immunogenic peptides derived from viral proteins. This study involved a retrospective review of historical influenza viruses circulating in human populations from 1918 to 2020 to identify evidence of prior circulation of H3N3v immunogenic CD8+ T‐cells peptides found in the NP and M1 proteins. We found evidence of prior circulation of H3N2v NP and M1 immunogenic peptides in historical influenza viruses. This provides insight into the population context in which influenza viruses emerge and may help inform immunogenic peptide selection for cytotoxic T‐cell lymphocytes (CTL)‐inducing influenza vaccines. Next‐generation vaccines capable of eliciting CD8+ T‐cell‐mediated cross‐protective immunity may offer a long‐term alternative strategy for influenza vaccines.
Highlights
Swine origin influenza viruses remain a continuing threat to human health.
Current influenza vaccines do not provide protection against novel influenza viruses.
CD8+ Tcell immunogenic peptides in the NP and M1 proteins of the H3N2v influenza viruses were investigated for evidence of prior circulation in human influenza viruses.
Vaccines based on common CD8+ Tcell immunogenic peptides may be able to mimic cross protection provided by influenza infection.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>34449904</pmid><doi>10.1002/jmv.27299</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-8751-5730</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Aged Animals B-Lymphocytes - immunology CD8 antigen CD8-Positive T-Lymphocytes - immunology Child Child, Preschool Cross Protection Cytotoxicity Disease Outbreaks Female H3N2v Health risks Human populations Humans immunogenic Immunogenicity Infant Infections Influenza Influenza A Influenza A Virus, H3N2 Subtype - genetics Influenza A Virus, H3N2 Subtype - immunology Influenza, Human - immunology Influenza, Human - virology Lymphocytes Lymphocytes T Male Matrix protein Middle Aged Orthomyxoviridae Orthomyxoviridae Infections - immunology Orthomyxoviridae Infections - virology Outbreaks Pandemics Peptides Proteins Public health Retrospective Studies Swine Swine flu T-Lymphocytes, Cytotoxic - immunology Vaccines Virology Viruses Young Adult |
title | Likelihood of prior exposure to circulating influenza viruses resulting in cross‐protection by CD8+ T cells against emergent H3N2v swine viruses infecting humans |
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