Loading…

Time-dependent evolution of IgG antibody levels after first and second dose of mRNA-based SARS-CoV-2 vaccination in haemodialysis patients: a multicentre study

ABSTRACT Background Vaccination programs are essential for the containment of the coronavirus disease 2019 pandemic, which has hit haemodialysis populations especially hard. Early reports suggest a reduced immunologic response to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines...

Full description

Saved in:
Bibliographic Details
Published in:Nephrology, dialysis, transplantation dialysis, transplantation, 2022-01, Vol.37 (2), p.375-381
Main Authors: Santos-Araújo, Carla, Mota Veiga, Pedro, Santos, Mário João, Santos, Lidia, Romãozinho, Catarina, Silva, Mónica, Lucas, Carlos, Duarte, Mary Luz, Haarhaus, Mathias, Haase, Michael, Macário, Fernando
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c488t-c5b7d85f90eaeb82a0f237c455f08d5547586f46b2763fd6a69704c19ea984433
cites cdi_FETCH-LOGICAL-c488t-c5b7d85f90eaeb82a0f237c455f08d5547586f46b2763fd6a69704c19ea984433
container_end_page 381
container_issue 2
container_start_page 375
container_title Nephrology, dialysis, transplantation
container_volume 37
creator Santos-Araújo, Carla
Mota Veiga, Pedro
Santos, Mário João
Santos, Lidia
Romãozinho, Catarina
Silva, Mónica
Lucas, Carlos
Duarte, Mary Luz
Haarhaus, Mathias
Haase, Michael
Macário, Fernando
description ABSTRACT Background Vaccination programs are essential for the containment of the coronavirus disease 2019 pandemic, which has hit haemodialysis populations especially hard. Early reports suggest a reduced immunologic response to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines in dialysis patients, in spite of a high degree of seroconversion. We aimed to identify risk factors for a reduced efficacy of an mRNA vaccine in a cohort of haemodialysis patients. Method In a multicentre study, including 294 Portuguese haemodialysis patients who had received two doses of BNT162b2 with a 3-week interval, immunoglobulin G-class antibodies against the SARS-CoV-2 spike protein were determined 3 weeks after the first dose (M1) and 6 weeks after the second dose (M2). The threshold for seroconversion was 10 UR/mL. Demographic and clinical data were retrieved from a quality registry. Adverse events were registered using a questionnaire. Results At M2, seroconversion was 93.1% with a median antibody level of 197.5 U/mL (1.2–3237.0) and a median increase of 180.0 U/mL (−82.9 to 2244.6) from M1. Age [beta −8.9; 95% confidence interval (95% CI) −12.88 to −4.91; P 600 ng/mL (beta 183.93; 95% CI 74.75–293.10; P = 0.001) and physical activity (beta 265.79; 95% CI 30.7–500.88; P = 0.03) were independent predictors of SARS-CoV-2 antibody levels after two vaccine doses. Plasma albumin >3.5 g/dL independently predicted the increase of antibody levels between both doses (odds ratio 14.72; 95% CI 1.38 to 157.45; P = 0.03). Only mild adverse reactions were observed in 10.9% of patients. Conclusions The SARS-CoV-2 vaccine BNT162b2 is safe and effective in haemodialysis patients. Besides age, iron status and nutrition are possible modifiable modulators of the immunologic response to SARS-CoV-2 mRNA vaccines. These data suggest the need for an early identification of populations at higher risk for diminished antibody production and the potential advantage of the implementation of oriented strategies to maximize the immune response to vaccination in these patients. Graphical Abstract Graphical Abstract
doi_str_mv 10.1093/ndt/gfab293
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2581279223</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><oup_id>10.1093/ndt/gfab293</oup_id><sourcerecordid>2581279223</sourcerecordid><originalsourceid>FETCH-LOGICAL-c488t-c5b7d85f90eaeb82a0f237c455f08d5547586f46b2763fd6a69704c19ea984433</originalsourceid><addsrcrecordid>eNp9kU9v1DAQxS0EotvCiTvyCSEhU_9NbG6rFZRKVSu1hWvk2ONilMQhdlbaT8NXJdtdeuzpaeb95s3hIfSO0c-MGnE--HL-EGzLjXiBVkxWlHCh1Uu0WlxGqKLmBJ3m_JtSanhdv0YnQlZCMlat0N_72APxMMLgYSgYtqmbS0wDTgFfPlxgO5TYJr_DHWyhy9iGAhMOccpl8TzO4NIiPmXYn_S312vS2gwe361v78gm_SQcb61zcbCPuXHAvyz0yUfb7XLMeFz2y-v8BVvcz12JbpkmwLnMfvcGvQq2y_D2qGfox7ev95vv5Orm4nKzviJOal2IU23ttQqGgoVWc0sDF7WTSgWqvVKyVroKsmp5XYngK1uZmkrHDFijpRTiDH085I5T-jNDLk0fs4OuswOkOTdcacZrw_ke_XRA3ZRyniA04xR7O-0aRpt9I83SSHNsZKHfH4Pntgf_xP6vYAE-HIA0j88m_QNkdZaF</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2581279223</pqid></control><display><type>article</type><title>Time-dependent evolution of IgG antibody levels after first and second dose of mRNA-based SARS-CoV-2 vaccination in haemodialysis patients: a multicentre study</title><source>Oxford University Press:Jisc Collections:OUP Read and Publish 2024-2025 (2024 collection) (Reading list)</source><creator>Santos-Araújo, Carla ; Mota Veiga, Pedro ; Santos, Mário João ; Santos, Lidia ; Romãozinho, Catarina ; Silva, Mónica ; Lucas, Carlos ; Duarte, Mary Luz ; Haarhaus, Mathias ; Haase, Michael ; Macário, Fernando</creator><creatorcontrib>Santos-Araújo, Carla ; Mota Veiga, Pedro ; Santos, Mário João ; Santos, Lidia ; Romãozinho, Catarina ; Silva, Mónica ; Lucas, Carlos ; Duarte, Mary Luz ; Haarhaus, Mathias ; Haase, Michael ; Macário, Fernando</creatorcontrib><description>ABSTRACT Background Vaccination programs are essential for the containment of the coronavirus disease 2019 pandemic, which has hit haemodialysis populations especially hard. Early reports suggest a reduced immunologic response to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines in dialysis patients, in spite of a high degree of seroconversion. We aimed to identify risk factors for a reduced efficacy of an mRNA vaccine in a cohort of haemodialysis patients. Method In a multicentre study, including 294 Portuguese haemodialysis patients who had received two doses of BNT162b2 with a 3-week interval, immunoglobulin G-class antibodies against the SARS-CoV-2 spike protein were determined 3 weeks after the first dose (M1) and 6 weeks after the second dose (M2). The threshold for seroconversion was 10 UR/mL. Demographic and clinical data were retrieved from a quality registry. Adverse events were registered using a questionnaire. Results At M2, seroconversion was 93.1% with a median antibody level of 197.5 U/mL (1.2–3237.0) and a median increase of 180.0 U/mL (−82.9 to 2244.6) from M1. Age [beta −8.9; 95% confidence interval (95% CI) −12.88 to −4.91; P &lt; 0.0001], ferritin &gt;600 ng/mL (beta 183.93; 95% CI 74.75–293.10; P = 0.001) and physical activity (beta 265.79; 95% CI 30.7–500.88; P = 0.03) were independent predictors of SARS-CoV-2 antibody levels after two vaccine doses. Plasma albumin &gt;3.5 g/dL independently predicted the increase of antibody levels between both doses (odds ratio 14.72; 95% CI 1.38 to 157.45; P = 0.03). Only mild adverse reactions were observed in 10.9% of patients. Conclusions The SARS-CoV-2 vaccine BNT162b2 is safe and effective in haemodialysis patients. Besides age, iron status and nutrition are possible modifiable modulators of the immunologic response to SARS-CoV-2 mRNA vaccines. These data suggest the need for an early identification of populations at higher risk for diminished antibody production and the potential advantage of the implementation of oriented strategies to maximize the immune response to vaccination in these patients. Graphical Abstract Graphical Abstract</description><identifier>ISSN: 0931-0509</identifier><identifier>EISSN: 1460-2385</identifier><identifier>DOI: 10.1093/ndt/gfab293</identifier><identifier>PMID: 34634116</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Antibodies, Viral ; BNT162 Vaccine ; COVID-19 ; COVID-19 Vaccines ; Humans ; Immunogenicity, Vaccine ; Immunoglobulin G ; mRNA Vaccines ; Renal Dialysis ; SARS-CoV-2 ; Spike Glycoprotein, Coronavirus ; Vaccination ; Vaccines, Synthetic</subject><ispartof>Nephrology, dialysis, transplantation, 2022-01, Vol.37 (2), p.375-381</ispartof><rights>The Author(s) 2021. Published by Oxford University Press on behalf of the ERA. 2021</rights><rights>The Author(s) 2021. Published by Oxford University Press on behalf of the ERA.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c488t-c5b7d85f90eaeb82a0f237c455f08d5547586f46b2763fd6a69704c19ea984433</citedby><cites>FETCH-LOGICAL-c488t-c5b7d85f90eaeb82a0f237c455f08d5547586f46b2763fd6a69704c19ea984433</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34634116$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Santos-Araújo, Carla</creatorcontrib><creatorcontrib>Mota Veiga, Pedro</creatorcontrib><creatorcontrib>Santos, Mário João</creatorcontrib><creatorcontrib>Santos, Lidia</creatorcontrib><creatorcontrib>Romãozinho, Catarina</creatorcontrib><creatorcontrib>Silva, Mónica</creatorcontrib><creatorcontrib>Lucas, Carlos</creatorcontrib><creatorcontrib>Duarte, Mary Luz</creatorcontrib><creatorcontrib>Haarhaus, Mathias</creatorcontrib><creatorcontrib>Haase, Michael</creatorcontrib><creatorcontrib>Macário, Fernando</creatorcontrib><title>Time-dependent evolution of IgG antibody levels after first and second dose of mRNA-based SARS-CoV-2 vaccination in haemodialysis patients: a multicentre study</title><title>Nephrology, dialysis, transplantation</title><addtitle>Nephrol Dial Transplant</addtitle><description>ABSTRACT Background Vaccination programs are essential for the containment of the coronavirus disease 2019 pandemic, which has hit haemodialysis populations especially hard. Early reports suggest a reduced immunologic response to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines in dialysis patients, in spite of a high degree of seroconversion. We aimed to identify risk factors for a reduced efficacy of an mRNA vaccine in a cohort of haemodialysis patients. Method In a multicentre study, including 294 Portuguese haemodialysis patients who had received two doses of BNT162b2 with a 3-week interval, immunoglobulin G-class antibodies against the SARS-CoV-2 spike protein were determined 3 weeks after the first dose (M1) and 6 weeks after the second dose (M2). The threshold for seroconversion was 10 UR/mL. Demographic and clinical data were retrieved from a quality registry. Adverse events were registered using a questionnaire. Results At M2, seroconversion was 93.1% with a median antibody level of 197.5 U/mL (1.2–3237.0) and a median increase of 180.0 U/mL (−82.9 to 2244.6) from M1. Age [beta −8.9; 95% confidence interval (95% CI) −12.88 to −4.91; P &lt; 0.0001], ferritin &gt;600 ng/mL (beta 183.93; 95% CI 74.75–293.10; P = 0.001) and physical activity (beta 265.79; 95% CI 30.7–500.88; P = 0.03) were independent predictors of SARS-CoV-2 antibody levels after two vaccine doses. Plasma albumin &gt;3.5 g/dL independently predicted the increase of antibody levels between both doses (odds ratio 14.72; 95% CI 1.38 to 157.45; P = 0.03). Only mild adverse reactions were observed in 10.9% of patients. Conclusions The SARS-CoV-2 vaccine BNT162b2 is safe and effective in haemodialysis patients. Besides age, iron status and nutrition are possible modifiable modulators of the immunologic response to SARS-CoV-2 mRNA vaccines. These data suggest the need for an early identification of populations at higher risk for diminished antibody production and the potential advantage of the implementation of oriented strategies to maximize the immune response to vaccination in these patients. Graphical Abstract Graphical Abstract</description><subject>Antibodies, Viral</subject><subject>BNT162 Vaccine</subject><subject>COVID-19</subject><subject>COVID-19 Vaccines</subject><subject>Humans</subject><subject>Immunogenicity, Vaccine</subject><subject>Immunoglobulin G</subject><subject>mRNA Vaccines</subject><subject>Renal Dialysis</subject><subject>SARS-CoV-2</subject><subject>Spike Glycoprotein, Coronavirus</subject><subject>Vaccination</subject><subject>Vaccines, Synthetic</subject><issn>0931-0509</issn><issn>1460-2385</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kU9v1DAQxS0EotvCiTvyCSEhU_9NbG6rFZRKVSu1hWvk2ONilMQhdlbaT8NXJdtdeuzpaeb95s3hIfSO0c-MGnE--HL-EGzLjXiBVkxWlHCh1Uu0WlxGqKLmBJ3m_JtSanhdv0YnQlZCMlat0N_72APxMMLgYSgYtqmbS0wDTgFfPlxgO5TYJr_DHWyhy9iGAhMOccpl8TzO4NIiPmXYn_S312vS2gwe361v78gm_SQcb61zcbCPuXHAvyz0yUfb7XLMeFz2y-v8BVvcz12JbpkmwLnMfvcGvQq2y_D2qGfox7ev95vv5Orm4nKzviJOal2IU23ttQqGgoVWc0sDF7WTSgWqvVKyVroKsmp5XYngK1uZmkrHDFijpRTiDH085I5T-jNDLk0fs4OuswOkOTdcacZrw_ke_XRA3ZRyniA04xR7O-0aRpt9I83SSHNsZKHfH4Pntgf_xP6vYAE-HIA0j88m_QNkdZaF</recordid><startdate>20220125</startdate><enddate>20220125</enddate><creator>Santos-Araújo, Carla</creator><creator>Mota Veiga, Pedro</creator><creator>Santos, Mário João</creator><creator>Santos, Lidia</creator><creator>Romãozinho, Catarina</creator><creator>Silva, Mónica</creator><creator>Lucas, Carlos</creator><creator>Duarte, Mary Luz</creator><creator>Haarhaus, Mathias</creator><creator>Haase, Michael</creator><creator>Macário, Fernando</creator><general>Oxford University Press</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>7X8</scope></search><sort><creationdate>20220125</creationdate><title>Time-dependent evolution of IgG antibody levels after first and second dose of mRNA-based SARS-CoV-2 vaccination in haemodialysis patients: a multicentre study</title><author>Santos-Araújo, Carla ; Mota Veiga, Pedro ; Santos, Mário João ; Santos, Lidia ; Romãozinho, Catarina ; Silva, Mónica ; Lucas, Carlos ; Duarte, Mary Luz ; Haarhaus, Mathias ; Haase, Michael ; Macário, Fernando</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c488t-c5b7d85f90eaeb82a0f237c455f08d5547586f46b2763fd6a69704c19ea984433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Antibodies, Viral</topic><topic>BNT162 Vaccine</topic><topic>COVID-19</topic><topic>COVID-19 Vaccines</topic><topic>Humans</topic><topic>Immunogenicity, Vaccine</topic><topic>Immunoglobulin G</topic><topic>mRNA Vaccines</topic><topic>Renal Dialysis</topic><topic>SARS-CoV-2</topic><topic>Spike Glycoprotein, Coronavirus</topic><topic>Vaccination</topic><topic>Vaccines, Synthetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Santos-Araújo, Carla</creatorcontrib><creatorcontrib>Mota Veiga, Pedro</creatorcontrib><creatorcontrib>Santos, Mário João</creatorcontrib><creatorcontrib>Santos, Lidia</creatorcontrib><creatorcontrib>Romãozinho, Catarina</creatorcontrib><creatorcontrib>Silva, Mónica</creatorcontrib><creatorcontrib>Lucas, Carlos</creatorcontrib><creatorcontrib>Duarte, Mary Luz</creatorcontrib><creatorcontrib>Haarhaus, Mathias</creatorcontrib><creatorcontrib>Haase, Michael</creatorcontrib><creatorcontrib>Macário, Fernando</creatorcontrib><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>Nephrology, dialysis, transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Santos-Araújo, Carla</au><au>Mota Veiga, Pedro</au><au>Santos, Mário João</au><au>Santos, Lidia</au><au>Romãozinho, Catarina</au><au>Silva, Mónica</au><au>Lucas, Carlos</au><au>Duarte, Mary Luz</au><au>Haarhaus, Mathias</au><au>Haase, Michael</au><au>Macário, Fernando</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Time-dependent evolution of IgG antibody levels after first and second dose of mRNA-based SARS-CoV-2 vaccination in haemodialysis patients: a multicentre study</atitle><jtitle>Nephrology, dialysis, transplantation</jtitle><addtitle>Nephrol Dial Transplant</addtitle><date>2022-01-25</date><risdate>2022</risdate><volume>37</volume><issue>2</issue><spage>375</spage><epage>381</epage><pages>375-381</pages><issn>0931-0509</issn><eissn>1460-2385</eissn><abstract>ABSTRACT Background Vaccination programs are essential for the containment of the coronavirus disease 2019 pandemic, which has hit haemodialysis populations especially hard. Early reports suggest a reduced immunologic response to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines in dialysis patients, in spite of a high degree of seroconversion. We aimed to identify risk factors for a reduced efficacy of an mRNA vaccine in a cohort of haemodialysis patients. Method In a multicentre study, including 294 Portuguese haemodialysis patients who had received two doses of BNT162b2 with a 3-week interval, immunoglobulin G-class antibodies against the SARS-CoV-2 spike protein were determined 3 weeks after the first dose (M1) and 6 weeks after the second dose (M2). The threshold for seroconversion was 10 UR/mL. Demographic and clinical data were retrieved from a quality registry. Adverse events were registered using a questionnaire. Results At M2, seroconversion was 93.1% with a median antibody level of 197.5 U/mL (1.2–3237.0) and a median increase of 180.0 U/mL (−82.9 to 2244.6) from M1. Age [beta −8.9; 95% confidence interval (95% CI) −12.88 to −4.91; P &lt; 0.0001], ferritin &gt;600 ng/mL (beta 183.93; 95% CI 74.75–293.10; P = 0.001) and physical activity (beta 265.79; 95% CI 30.7–500.88; P = 0.03) were independent predictors of SARS-CoV-2 antibody levels after two vaccine doses. Plasma albumin &gt;3.5 g/dL independently predicted the increase of antibody levels between both doses (odds ratio 14.72; 95% CI 1.38 to 157.45; P = 0.03). Only mild adverse reactions were observed in 10.9% of patients. Conclusions The SARS-CoV-2 vaccine BNT162b2 is safe and effective in haemodialysis patients. Besides age, iron status and nutrition are possible modifiable modulators of the immunologic response to SARS-CoV-2 mRNA vaccines. These data suggest the need for an early identification of populations at higher risk for diminished antibody production and the potential advantage of the implementation of oriented strategies to maximize the immune response to vaccination in these patients. Graphical Abstract Graphical Abstract</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>34634116</pmid><doi>10.1093/ndt/gfab293</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0931-0509
ispartof Nephrology, dialysis, transplantation, 2022-01, Vol.37 (2), p.375-381
issn 0931-0509
1460-2385
language eng
recordid cdi_proquest_miscellaneous_2581279223
source Oxford University Press:Jisc Collections:OUP Read and Publish 2024-2025 (2024 collection) (Reading list)
subjects Antibodies, Viral
BNT162 Vaccine
COVID-19
COVID-19 Vaccines
Humans
Immunogenicity, Vaccine
Immunoglobulin G
mRNA Vaccines
Renal Dialysis
SARS-CoV-2
Spike Glycoprotein, Coronavirus
Vaccination
Vaccines, Synthetic
title Time-dependent evolution of IgG antibody levels after first and second dose of mRNA-based SARS-CoV-2 vaccination in haemodialysis patients: a multicentre study
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T00%3A57%3A58IST&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=Time-dependent%20evolution%20of%20IgG%20antibody%20levels%20after%20first%20and%20second%20dose%20of%20mRNA-based%20SARS-CoV-2%20vaccination%20in%20haemodialysis%20patients:%20a%20multicentre%20study&rft.jtitle=Nephrology,%20dialysis,%20transplantation&rft.au=Santos-Ara%C3%BAjo,%20Carla&rft.date=2022-01-25&rft.volume=37&rft.issue=2&rft.spage=375&rft.epage=381&rft.pages=375-381&rft.issn=0931-0509&rft.eissn=1460-2385&rft_id=info:doi/10.1093/ndt/gfab293&rft_dat=%3Cproquest_cross%3E2581279223%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c488t-c5b7d85f90eaeb82a0f237c455f08d5547586f46b2763fd6a69704c19ea984433%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2581279223&rft_id=info:pmid/34634116&rft_oup_id=10.1093/ndt/gfab293&rfr_iscdi=true