Generation of cardio-protective antibodies after pneumococcal polysaccharide vaccine: Early results from a randomised controlled trial
Observational studies have demonstrated that the pneumococcal polysaccharide vaccine (PPV) is associated with reduced risk of cardiovascular events. This may be mediated through IgM antibodies to OxLDL, which have previously been associated with cardioprotective effects. The Australian Study for the...
Gespeichert in:
Veröffentlicht in: | Atherosclerosis 2022-04, Vol.346, p.68-74 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 74 |
---|---|
container_issue | |
container_start_page | 68 |
container_title | Atherosclerosis |
container_volume | 346 |
creator | Ren, Shu Hansbro, Philip M. Srikusalanukul, Wichat Horvat, Jay C. Hunter, Tegan Brown, Alexandra C. Peel, Roseanne Faulkner, Jack Evans, Tiffany-Jane Li, Shu Chuen Newby, David Hure, Alexis Abhayaratna, Walter P. Tsimikas, Sotirios Gonen, Ayelet Witztum, Joseph L. Attia, John Ren, Shu Hansbro, Philip M. Peel, Roseanne Srikusalanukul, Wichat Abhayaratna, Walter Newby, David Hure, Alexis D'Este, Catherine Tonkin, Andrew Hopper, Ingrid Thrift, Amanda Levi, Christopher Sturm, Jonathan Durrheim, David Hung, Joseph Briffa, Tom Chew, Derek Anderson, Phil Moon, Lynelle McEvoy, Mark Attia, John |
description | Observational studies have demonstrated that the pneumococcal polysaccharide vaccine (PPV) is associated with reduced risk of cardiovascular events. This may be mediated through IgM antibodies to OxLDL, which have previously been associated with cardioprotective effects. The Australian Study for the Prevention through Immunisation of Cardiovascular Events (AUSPICE) is a double-blind, randomised controlled trial (RCT) of PPV in preventing ischaemic events. Participants received PPV or placebo once at baseline and are being followed-up for incident fatal and non-fatal myocardial infarction or stroke over 6 years.
A subgroup of participants at one centre (Canberra; n = 1,001) were evaluated at 1 month and 2 years post immunisation for changes in surrogate markers of atherosclerosis, as pre-specified secondary outcomes: high-sensitive C-reactive protein (CRP), pulse wave velocity (PWV), and carotid intima-media thickness (CIMT). In addition, 100 participants were randomly selected in each of the intervention and control groups for measurement of anti-pneumococcal antibodies (IgG, IgG2, IgM) as well as anti-OxLDL antibodies (IgG and IgM to CuOxLDL, MDA-LDL, and PC-KLH).
Concentrations of anti-pneumococcal IgG and IgG2 increased and remained high at 2 years in the PPV group compared to the placebo group, while IgM increased and then declined, but remained detectable, at 2 years. There were statistically significant increases in all anti-OxLDL IgM antibodies at 1 month, which were no longer detectable at 2 years; there was no increase in anti-OxLDL IgG antibodies. There were no significant changes in CRP, PWV or CIMT between the treatment groups at the 2-year follow-up.
PPV engenders a long-lasting increase in anti-pneumococcal IgG, and to a lesser extent, IgM titres, as well as a transient increase in anti-OxLDL IgM antibodies. However, there were no detectable changes in surrogate markers of atherosclerosis at the 2-year follow-up. Long-term, prospective follow-up of clinical outcomes is continuing to assess if PPV reduces CVD events.
[Display omitted]
•In mice, immunisation against Pneumococcus elicits anti-oxLDL antibodies which inhibit atherosclerotic plaque growth•We provide the first RCT evidence in humans that the pneumococcal polysaccharide vaccine elicits the same protective anti-oxLDL antibodies at 1 month.•By 2 years, these antibodies have returned to baseline levels and do not have any measurable effect on surrogate markers of CVD, including CRP, pul |
doi_str_mv | 10.1016/j.atherosclerosis.2022.02.011 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2640047938</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0021915022000806</els_id><sourcerecordid>2640047938</sourcerecordid><originalsourceid>FETCH-LOGICAL-c444t-f4c2f97897bd0c932b5fecc1f8cecee75d49543af4346b24085e8f0cea4a0883</originalsourceid><addsrcrecordid>eNqNUcGKFDEQDaK4s6u_ILkIXnpMutPTacGDLOsoLHjZe0hXKmyGdDIm6YH5Ab9708zqYU9CUVWHV_Wq3iPkI2dbzvju82GryyOmmMGv2eVty9p2y2pw_opsuBzGhgspXpMNYy1vRt6zK3Kd84ExJgYu35Krrm9HJnm3IX_2GDDp4mKg0VLQybjYHFMsCMWdkOpQ3BSNw0y1LZjoMeAyR4gA2tNj9OesAR51cgbpqbYu4Bd6p5M_04R58SVTm-JMNU06mDi7jIZCDCVF72tbktP-HXljtc_4_rnekIfvdw-3P5r7X_uft9_uGxBClMYKaO04yHGYDIOxa6feIgC3EhAQh96IsRedtqITu6kVTPYoLQPUQjMpuxvy6bK2Pvh7wVxUPQfQex0wLlm1O7FqNHYr9OsFClXlnNCqY3KzTmfFmVqdUAf1wgm1OqFYDc7r_IdnqmWa0fyb_it9BewvAKz_nhwmlcFhADQuVe2Vie4_qZ4AbqGolA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2640047938</pqid></control><display><type>article</type><title>Generation of cardio-protective antibodies after pneumococcal polysaccharide vaccine: Early results from a randomised controlled trial</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Ren, Shu ; Hansbro, Philip M. ; Srikusalanukul, Wichat ; Horvat, Jay C. ; Hunter, Tegan ; Brown, Alexandra C. ; Peel, Roseanne ; Faulkner, Jack ; Evans, Tiffany-Jane ; Li, Shu Chuen ; Newby, David ; Hure, Alexis ; Abhayaratna, Walter P. ; Tsimikas, Sotirios ; Gonen, Ayelet ; Witztum, Joseph L. ; Attia, John ; Ren, Shu ; Hansbro, Philip M. ; Peel, Roseanne ; Srikusalanukul, Wichat ; Abhayaratna, Walter ; Newby, David ; Hure, Alexis ; D'Este, Catherine ; Tonkin, Andrew ; Hopper, Ingrid ; Thrift, Amanda ; Levi, Christopher ; Sturm, Jonathan ; Durrheim, David ; Hung, Joseph ; Briffa, Tom ; Chew, Derek ; Anderson, Phil ; Moon, Lynelle ; McEvoy, Mark ; Attia, John</creator><creatorcontrib>Ren, Shu ; Hansbro, Philip M. ; Srikusalanukul, Wichat ; Horvat, Jay C. ; Hunter, Tegan ; Brown, Alexandra C. ; Peel, Roseanne ; Faulkner, Jack ; Evans, Tiffany-Jane ; Li, Shu Chuen ; Newby, David ; Hure, Alexis ; Abhayaratna, Walter P. ; Tsimikas, Sotirios ; Gonen, Ayelet ; Witztum, Joseph L. ; Attia, John ; Ren, Shu ; Hansbro, Philip M. ; Peel, Roseanne ; Srikusalanukul, Wichat ; Abhayaratna, Walter ; Newby, David ; Hure, Alexis ; D'Este, Catherine ; Tonkin, Andrew ; Hopper, Ingrid ; Thrift, Amanda ; Levi, Christopher ; Sturm, Jonathan ; Durrheim, David ; Hung, Joseph ; Briffa, Tom ; Chew, Derek ; Anderson, Phil ; Moon, Lynelle ; McEvoy, Mark ; Attia, John ; The AUSPICE investigators ; AUSPICE investigators</creatorcontrib><description>Observational studies have demonstrated that the pneumococcal polysaccharide vaccine (PPV) is associated with reduced risk of cardiovascular events. This may be mediated through IgM antibodies to OxLDL, which have previously been associated with cardioprotective effects. The Australian Study for the Prevention through Immunisation of Cardiovascular Events (AUSPICE) is a double-blind, randomised controlled trial (RCT) of PPV in preventing ischaemic events. Participants received PPV or placebo once at baseline and are being followed-up for incident fatal and non-fatal myocardial infarction or stroke over 6 years.
A subgroup of participants at one centre (Canberra; n = 1,001) were evaluated at 1 month and 2 years post immunisation for changes in surrogate markers of atherosclerosis, as pre-specified secondary outcomes: high-sensitive C-reactive protein (CRP), pulse wave velocity (PWV), and carotid intima-media thickness (CIMT). In addition, 100 participants were randomly selected in each of the intervention and control groups for measurement of anti-pneumococcal antibodies (IgG, IgG2, IgM) as well as anti-OxLDL antibodies (IgG and IgM to CuOxLDL, MDA-LDL, and PC-KLH).
Concentrations of anti-pneumococcal IgG and IgG2 increased and remained high at 2 years in the PPV group compared to the placebo group, while IgM increased and then declined, but remained detectable, at 2 years. There were statistically significant increases in all anti-OxLDL IgM antibodies at 1 month, which were no longer detectable at 2 years; there was no increase in anti-OxLDL IgG antibodies. There were no significant changes in CRP, PWV or CIMT between the treatment groups at the 2-year follow-up.
PPV engenders a long-lasting increase in anti-pneumococcal IgG, and to a lesser extent, IgM titres, as well as a transient increase in anti-OxLDL IgM antibodies. However, there were no detectable changes in surrogate markers of atherosclerosis at the 2-year follow-up. Long-term, prospective follow-up of clinical outcomes is continuing to assess if PPV reduces CVD events.
[Display omitted]
•In mice, immunisation against Pneumococcus elicits anti-oxLDL antibodies which inhibit atherosclerotic plaque growth•We provide the first RCT evidence in humans that the pneumococcal polysaccharide vaccine elicits the same protective anti-oxLDL antibodies at 1 month.•By 2 years, these antibodies have returned to baseline levels and do not have any measurable effect on surrogate markers of CVD, including CRP, pulse wave velocity or carotid intima-media thickness</description><identifier>ISSN: 0021-9150</identifier><identifier>EISSN: 1879-1484</identifier><identifier>DOI: 10.1016/j.atherosclerosis.2022.02.011</identifier><identifier>PMID: 35290813</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>Anti-oxLDL antibodies ; Anti-pneumococcal antibodies ; Atherosclerosis ; Atherosclerosis - prevention & control ; Australia ; Biomarkers ; Cardiovascular disease ; Human clinical trial ; Humans ; Immunoglobulin G ; Immunoglobulin M ; Oxidative stress ; Pneumococcal vaccine ; Pneumococcal Vaccines ; Streptococcus pneumoniae</subject><ispartof>Atherosclerosis, 2022-04, Vol.346, p.68-74</ispartof><rights>2022 The Authors</rights><rights>Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c444t-f4c2f97897bd0c932b5fecc1f8cecee75d49543af4346b24085e8f0cea4a0883</citedby><cites>FETCH-LOGICAL-c444t-f4c2f97897bd0c932b5fecc1f8cecee75d49543af4346b24085e8f0cea4a0883</cites><orcidid>0000-0002-4741-3035 ; 0000-0003-2225-0986 ; 0000-0001-9800-1308 ; 0000-0003-0791-7228 ; 0000-0001-9834-9494 ; 0000-0001-9912-3198</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0021915022000806$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35290813$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ren, Shu</creatorcontrib><creatorcontrib>Hansbro, Philip M.</creatorcontrib><creatorcontrib>Srikusalanukul, Wichat</creatorcontrib><creatorcontrib>Horvat, Jay C.</creatorcontrib><creatorcontrib>Hunter, Tegan</creatorcontrib><creatorcontrib>Brown, Alexandra C.</creatorcontrib><creatorcontrib>Peel, Roseanne</creatorcontrib><creatorcontrib>Faulkner, Jack</creatorcontrib><creatorcontrib>Evans, Tiffany-Jane</creatorcontrib><creatorcontrib>Li, Shu Chuen</creatorcontrib><creatorcontrib>Newby, David</creatorcontrib><creatorcontrib>Hure, Alexis</creatorcontrib><creatorcontrib>Abhayaratna, Walter P.</creatorcontrib><creatorcontrib>Tsimikas, Sotirios</creatorcontrib><creatorcontrib>Gonen, Ayelet</creatorcontrib><creatorcontrib>Witztum, Joseph L.</creatorcontrib><creatorcontrib>Attia, John</creatorcontrib><creatorcontrib>Ren, Shu</creatorcontrib><creatorcontrib>Hansbro, Philip M.</creatorcontrib><creatorcontrib>Peel, Roseanne</creatorcontrib><creatorcontrib>Srikusalanukul, Wichat</creatorcontrib><creatorcontrib>Abhayaratna, Walter</creatorcontrib><creatorcontrib>Newby, David</creatorcontrib><creatorcontrib>Hure, Alexis</creatorcontrib><creatorcontrib>D'Este, Catherine</creatorcontrib><creatorcontrib>Tonkin, Andrew</creatorcontrib><creatorcontrib>Hopper, Ingrid</creatorcontrib><creatorcontrib>Thrift, Amanda</creatorcontrib><creatorcontrib>Levi, Christopher</creatorcontrib><creatorcontrib>Sturm, Jonathan</creatorcontrib><creatorcontrib>Durrheim, David</creatorcontrib><creatorcontrib>Hung, Joseph</creatorcontrib><creatorcontrib>Briffa, Tom</creatorcontrib><creatorcontrib>Chew, Derek</creatorcontrib><creatorcontrib>Anderson, Phil</creatorcontrib><creatorcontrib>Moon, Lynelle</creatorcontrib><creatorcontrib>McEvoy, Mark</creatorcontrib><creatorcontrib>Attia, John</creatorcontrib><creatorcontrib>The AUSPICE investigators</creatorcontrib><creatorcontrib>AUSPICE investigators</creatorcontrib><title>Generation of cardio-protective antibodies after pneumococcal polysaccharide vaccine: Early results from a randomised controlled trial</title><title>Atherosclerosis</title><addtitle>Atherosclerosis</addtitle><description>Observational studies have demonstrated that the pneumococcal polysaccharide vaccine (PPV) is associated with reduced risk of cardiovascular events. This may be mediated through IgM antibodies to OxLDL, which have previously been associated with cardioprotective effects. The Australian Study for the Prevention through Immunisation of Cardiovascular Events (AUSPICE) is a double-blind, randomised controlled trial (RCT) of PPV in preventing ischaemic events. Participants received PPV or placebo once at baseline and are being followed-up for incident fatal and non-fatal myocardial infarction or stroke over 6 years.
A subgroup of participants at one centre (Canberra; n = 1,001) were evaluated at 1 month and 2 years post immunisation for changes in surrogate markers of atherosclerosis, as pre-specified secondary outcomes: high-sensitive C-reactive protein (CRP), pulse wave velocity (PWV), and carotid intima-media thickness (CIMT). In addition, 100 participants were randomly selected in each of the intervention and control groups for measurement of anti-pneumococcal antibodies (IgG, IgG2, IgM) as well as anti-OxLDL antibodies (IgG and IgM to CuOxLDL, MDA-LDL, and PC-KLH).
Concentrations of anti-pneumococcal IgG and IgG2 increased and remained high at 2 years in the PPV group compared to the placebo group, while IgM increased and then declined, but remained detectable, at 2 years. There were statistically significant increases in all anti-OxLDL IgM antibodies at 1 month, which were no longer detectable at 2 years; there was no increase in anti-OxLDL IgG antibodies. There were no significant changes in CRP, PWV or CIMT between the treatment groups at the 2-year follow-up.
PPV engenders a long-lasting increase in anti-pneumococcal IgG, and to a lesser extent, IgM titres, as well as a transient increase in anti-OxLDL IgM antibodies. However, there were no detectable changes in surrogate markers of atherosclerosis at the 2-year follow-up. Long-term, prospective follow-up of clinical outcomes is continuing to assess if PPV reduces CVD events.
[Display omitted]
•In mice, immunisation against Pneumococcus elicits anti-oxLDL antibodies which inhibit atherosclerotic plaque growth•We provide the first RCT evidence in humans that the pneumococcal polysaccharide vaccine elicits the same protective anti-oxLDL antibodies at 1 month.•By 2 years, these antibodies have returned to baseline levels and do not have any measurable effect on surrogate markers of CVD, including CRP, pulse wave velocity or carotid intima-media thickness</description><subject>Anti-oxLDL antibodies</subject><subject>Anti-pneumococcal antibodies</subject><subject>Atherosclerosis</subject><subject>Atherosclerosis - prevention & control</subject><subject>Australia</subject><subject>Biomarkers</subject><subject>Cardiovascular disease</subject><subject>Human clinical trial</subject><subject>Humans</subject><subject>Immunoglobulin G</subject><subject>Immunoglobulin M</subject><subject>Oxidative stress</subject><subject>Pneumococcal vaccine</subject><subject>Pneumococcal Vaccines</subject><subject>Streptococcus pneumoniae</subject><issn>0021-9150</issn><issn>1879-1484</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNUcGKFDEQDaK4s6u_ILkIXnpMutPTacGDLOsoLHjZe0hXKmyGdDIm6YH5Ab9708zqYU9CUVWHV_Wq3iPkI2dbzvju82GryyOmmMGv2eVty9p2y2pw_opsuBzGhgspXpMNYy1vRt6zK3Kd84ExJgYu35Krrm9HJnm3IX_2GDDp4mKg0VLQybjYHFMsCMWdkOpQ3BSNw0y1LZjoMeAyR4gA2tNj9OesAR51cgbpqbYu4Bd6p5M_04R58SVTm-JMNU06mDi7jIZCDCVF72tbktP-HXljtc_4_rnekIfvdw-3P5r7X_uft9_uGxBClMYKaO04yHGYDIOxa6feIgC3EhAQh96IsRedtqITu6kVTPYoLQPUQjMpuxvy6bK2Pvh7wVxUPQfQex0wLlm1O7FqNHYr9OsFClXlnNCqY3KzTmfFmVqdUAf1wgm1OqFYDc7r_IdnqmWa0fyb_it9BewvAKz_nhwmlcFhADQuVe2Vie4_qZ4AbqGolA</recordid><startdate>202204</startdate><enddate>202204</enddate><creator>Ren, Shu</creator><creator>Hansbro, Philip M.</creator><creator>Srikusalanukul, Wichat</creator><creator>Horvat, Jay C.</creator><creator>Hunter, Tegan</creator><creator>Brown, Alexandra C.</creator><creator>Peel, Roseanne</creator><creator>Faulkner, Jack</creator><creator>Evans, Tiffany-Jane</creator><creator>Li, Shu Chuen</creator><creator>Newby, David</creator><creator>Hure, Alexis</creator><creator>Abhayaratna, Walter P.</creator><creator>Tsimikas, Sotirios</creator><creator>Gonen, Ayelet</creator><creator>Witztum, Joseph L.</creator><creator>Attia, John</creator><creator>Ren, Shu</creator><creator>Hansbro, Philip M.</creator><creator>Peel, Roseanne</creator><creator>Srikusalanukul, Wichat</creator><creator>Abhayaratna, Walter</creator><creator>Newby, David</creator><creator>Hure, Alexis</creator><creator>D'Este, Catherine</creator><creator>Tonkin, Andrew</creator><creator>Hopper, Ingrid</creator><creator>Thrift, Amanda</creator><creator>Levi, Christopher</creator><creator>Sturm, Jonathan</creator><creator>Durrheim, David</creator><creator>Hung, Joseph</creator><creator>Briffa, Tom</creator><creator>Chew, Derek</creator><creator>Anderson, Phil</creator><creator>Moon, Lynelle</creator><creator>McEvoy, Mark</creator><creator>Attia, John</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><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>7X8</scope><orcidid>https://orcid.org/0000-0002-4741-3035</orcidid><orcidid>https://orcid.org/0000-0003-2225-0986</orcidid><orcidid>https://orcid.org/0000-0001-9800-1308</orcidid><orcidid>https://orcid.org/0000-0003-0791-7228</orcidid><orcidid>https://orcid.org/0000-0001-9834-9494</orcidid><orcidid>https://orcid.org/0000-0001-9912-3198</orcidid></search><sort><creationdate>202204</creationdate><title>Generation of cardio-protective antibodies after pneumococcal polysaccharide vaccine: Early results from a randomised controlled trial</title><author>Ren, Shu ; Hansbro, Philip M. ; Srikusalanukul, Wichat ; Horvat, Jay C. ; Hunter, Tegan ; Brown, Alexandra C. ; Peel, Roseanne ; Faulkner, Jack ; Evans, Tiffany-Jane ; Li, Shu Chuen ; Newby, David ; Hure, Alexis ; Abhayaratna, Walter P. ; Tsimikas, Sotirios ; Gonen, Ayelet ; Witztum, Joseph L. ; Attia, John ; Ren, Shu ; Hansbro, Philip M. ; Peel, Roseanne ; Srikusalanukul, Wichat ; Abhayaratna, Walter ; Newby, David ; Hure, Alexis ; D'Este, Catherine ; Tonkin, Andrew ; Hopper, Ingrid ; Thrift, Amanda ; Levi, Christopher ; Sturm, Jonathan ; Durrheim, David ; Hung, Joseph ; Briffa, Tom ; Chew, Derek ; Anderson, Phil ; Moon, Lynelle ; McEvoy, Mark ; Attia, John</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c444t-f4c2f97897bd0c932b5fecc1f8cecee75d49543af4346b24085e8f0cea4a0883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Anti-oxLDL antibodies</topic><topic>Anti-pneumococcal antibodies</topic><topic>Atherosclerosis</topic><topic>Atherosclerosis - prevention & control</topic><topic>Australia</topic><topic>Biomarkers</topic><topic>Cardiovascular disease</topic><topic>Human clinical trial</topic><topic>Humans</topic><topic>Immunoglobulin G</topic><topic>Immunoglobulin M</topic><topic>Oxidative stress</topic><topic>Pneumococcal vaccine</topic><topic>Pneumococcal Vaccines</topic><topic>Streptococcus pneumoniae</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ren, Shu</creatorcontrib><creatorcontrib>Hansbro, Philip M.</creatorcontrib><creatorcontrib>Srikusalanukul, Wichat</creatorcontrib><creatorcontrib>Horvat, Jay C.</creatorcontrib><creatorcontrib>Hunter, Tegan</creatorcontrib><creatorcontrib>Brown, Alexandra C.</creatorcontrib><creatorcontrib>Peel, Roseanne</creatorcontrib><creatorcontrib>Faulkner, Jack</creatorcontrib><creatorcontrib>Evans, Tiffany-Jane</creatorcontrib><creatorcontrib>Li, Shu Chuen</creatorcontrib><creatorcontrib>Newby, David</creatorcontrib><creatorcontrib>Hure, Alexis</creatorcontrib><creatorcontrib>Abhayaratna, Walter P.</creatorcontrib><creatorcontrib>Tsimikas, Sotirios</creatorcontrib><creatorcontrib>Gonen, Ayelet</creatorcontrib><creatorcontrib>Witztum, Joseph L.</creatorcontrib><creatorcontrib>Attia, John</creatorcontrib><creatorcontrib>Ren, Shu</creatorcontrib><creatorcontrib>Hansbro, Philip M.</creatorcontrib><creatorcontrib>Peel, Roseanne</creatorcontrib><creatorcontrib>Srikusalanukul, Wichat</creatorcontrib><creatorcontrib>Abhayaratna, Walter</creatorcontrib><creatorcontrib>Newby, David</creatorcontrib><creatorcontrib>Hure, Alexis</creatorcontrib><creatorcontrib>D'Este, Catherine</creatorcontrib><creatorcontrib>Tonkin, Andrew</creatorcontrib><creatorcontrib>Hopper, Ingrid</creatorcontrib><creatorcontrib>Thrift, Amanda</creatorcontrib><creatorcontrib>Levi, Christopher</creatorcontrib><creatorcontrib>Sturm, Jonathan</creatorcontrib><creatorcontrib>Durrheim, David</creatorcontrib><creatorcontrib>Hung, Joseph</creatorcontrib><creatorcontrib>Briffa, Tom</creatorcontrib><creatorcontrib>Chew, Derek</creatorcontrib><creatorcontrib>Anderson, Phil</creatorcontrib><creatorcontrib>Moon, Lynelle</creatorcontrib><creatorcontrib>McEvoy, Mark</creatorcontrib><creatorcontrib>Attia, John</creatorcontrib><creatorcontrib>The AUSPICE investigators</creatorcontrib><creatorcontrib>AUSPICE investigators</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Atherosclerosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ren, Shu</au><au>Hansbro, Philip M.</au><au>Srikusalanukul, Wichat</au><au>Horvat, Jay C.</au><au>Hunter, Tegan</au><au>Brown, Alexandra C.</au><au>Peel, Roseanne</au><au>Faulkner, Jack</au><au>Evans, Tiffany-Jane</au><au>Li, Shu Chuen</au><au>Newby, David</au><au>Hure, Alexis</au><au>Abhayaratna, Walter P.</au><au>Tsimikas, Sotirios</au><au>Gonen, Ayelet</au><au>Witztum, Joseph L.</au><au>Attia, John</au><au>Ren, Shu</au><au>Hansbro, Philip M.</au><au>Peel, Roseanne</au><au>Srikusalanukul, Wichat</au><au>Abhayaratna, Walter</au><au>Newby, David</au><au>Hure, Alexis</au><au>D'Este, Catherine</au><au>Tonkin, Andrew</au><au>Hopper, Ingrid</au><au>Thrift, Amanda</au><au>Levi, Christopher</au><au>Sturm, Jonathan</au><au>Durrheim, David</au><au>Hung, Joseph</au><au>Briffa, Tom</au><au>Chew, Derek</au><au>Anderson, Phil</au><au>Moon, Lynelle</au><au>McEvoy, Mark</au><au>Attia, John</au><aucorp>The AUSPICE investigators</aucorp><aucorp>AUSPICE investigators</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Generation of cardio-protective antibodies after pneumococcal polysaccharide vaccine: Early results from a randomised controlled trial</atitle><jtitle>Atherosclerosis</jtitle><addtitle>Atherosclerosis</addtitle><date>2022-04</date><risdate>2022</risdate><volume>346</volume><spage>68</spage><epage>74</epage><pages>68-74</pages><issn>0021-9150</issn><eissn>1879-1484</eissn><abstract>Observational studies have demonstrated that the pneumococcal polysaccharide vaccine (PPV) is associated with reduced risk of cardiovascular events. This may be mediated through IgM antibodies to OxLDL, which have previously been associated with cardioprotective effects. The Australian Study for the Prevention through Immunisation of Cardiovascular Events (AUSPICE) is a double-blind, randomised controlled trial (RCT) of PPV in preventing ischaemic events. Participants received PPV or placebo once at baseline and are being followed-up for incident fatal and non-fatal myocardial infarction or stroke over 6 years.
A subgroup of participants at one centre (Canberra; n = 1,001) were evaluated at 1 month and 2 years post immunisation for changes in surrogate markers of atherosclerosis, as pre-specified secondary outcomes: high-sensitive C-reactive protein (CRP), pulse wave velocity (PWV), and carotid intima-media thickness (CIMT). In addition, 100 participants were randomly selected in each of the intervention and control groups for measurement of anti-pneumococcal antibodies (IgG, IgG2, IgM) as well as anti-OxLDL antibodies (IgG and IgM to CuOxLDL, MDA-LDL, and PC-KLH).
Concentrations of anti-pneumococcal IgG and IgG2 increased and remained high at 2 years in the PPV group compared to the placebo group, while IgM increased and then declined, but remained detectable, at 2 years. There were statistically significant increases in all anti-OxLDL IgM antibodies at 1 month, which were no longer detectable at 2 years; there was no increase in anti-OxLDL IgG antibodies. There were no significant changes in CRP, PWV or CIMT between the treatment groups at the 2-year follow-up.
PPV engenders a long-lasting increase in anti-pneumococcal IgG, and to a lesser extent, IgM titres, as well as a transient increase in anti-OxLDL IgM antibodies. However, there were no detectable changes in surrogate markers of atherosclerosis at the 2-year follow-up. Long-term, prospective follow-up of clinical outcomes is continuing to assess if PPV reduces CVD events.
[Display omitted]
•In mice, immunisation against Pneumococcus elicits anti-oxLDL antibodies which inhibit atherosclerotic plaque growth•We provide the first RCT evidence in humans that the pneumococcal polysaccharide vaccine elicits the same protective anti-oxLDL antibodies at 1 month.•By 2 years, these antibodies have returned to baseline levels and do not have any measurable effect on surrogate markers of CVD, including CRP, pulse wave velocity or carotid intima-media thickness</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>35290813</pmid><doi>10.1016/j.atherosclerosis.2022.02.011</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-4741-3035</orcidid><orcidid>https://orcid.org/0000-0003-2225-0986</orcidid><orcidid>https://orcid.org/0000-0001-9800-1308</orcidid><orcidid>https://orcid.org/0000-0003-0791-7228</orcidid><orcidid>https://orcid.org/0000-0001-9834-9494</orcidid><orcidid>https://orcid.org/0000-0001-9912-3198</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9150 |
ispartof | Atherosclerosis, 2022-04, Vol.346, p.68-74 |
issn | 0021-9150 1879-1484 |
language | eng |
recordid | cdi_proquest_miscellaneous_2640047938 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Anti-oxLDL antibodies Anti-pneumococcal antibodies Atherosclerosis Atherosclerosis - prevention & control Australia Biomarkers Cardiovascular disease Human clinical trial Humans Immunoglobulin G Immunoglobulin M Oxidative stress Pneumococcal vaccine Pneumococcal Vaccines Streptococcus pneumoniae |
title | Generation of cardio-protective antibodies after pneumococcal polysaccharide vaccine: Early results from a randomised controlled trial |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T04%3A13%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Generation%20of%20cardio-protective%20antibodies%20after%20pneumococcal%20polysaccharide%20vaccine:%20Early%20results%20from%20a%20randomised%20controlled%20trial&rft.jtitle=Atherosclerosis&rft.au=Ren,%20Shu&rft.aucorp=The%20AUSPICE%20investigators&rft.date=2022-04&rft.volume=346&rft.spage=68&rft.epage=74&rft.pages=68-74&rft.issn=0021-9150&rft.eissn=1879-1484&rft_id=info:doi/10.1016/j.atherosclerosis.2022.02.011&rft_dat=%3Cproquest_cross%3E2640047938%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2640047938&rft_id=info:pmid/35290813&rft_els_id=S0021915022000806&rfr_iscdi=true |