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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...
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Published in: | Nephrology, dialysis, transplantation dialysis, transplantation, 2022-01, Vol.37 (2), p.375-381 |
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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 |
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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 < 0.0001], ferritin >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</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 < 0.0001], ferritin >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</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 < 0.0001], ferritin >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</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> |
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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 |
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