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...

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Veröffentlicht in:Atherosclerosis 2022-04, Vol.346, p.68-74
Hauptverfasser: 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, Abhayaratna, Walter, 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
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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
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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 &amp; 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. 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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 &amp; 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 ; 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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>
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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
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