Humoral response after SARS-CoV-2 mRNA vaccines in dialysis patients: Integrating anti-SARS-CoV-2 Spike-Protein-RBD antibody monitoring to manage dialysis centers in pandemic times
Dialysis patients are both the most likely to benefit from vaccine protection against SARS-CoV-2 and at the highest risk of not developing an immune response. Data from the medical field are thus mandatory. We report our experience with a BNT162b2-mRNA vaccine in a retrospective analysis of 241 dial...
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description | Dialysis patients are both the most likely to benefit from vaccine protection against SARS-CoV-2 and at the highest risk of not developing an immune response. Data from the medical field are thus mandatory. We report our experience with a BNT162b2-mRNA vaccine in a retrospective analysis of 241 dialysis patients including 193 who underwent anti-Spike-Protein-Receptor-Binding-Domain (RBD) IgG analysis. We show that a pro-active vaccine campaign is effective in convincing most patients to be vaccinated (95%) and frequently elicits a specific antibody response (94.3% after two doses and 98.4% after three doses). Only immunocompromised Status is associated with lack of seroconversion (OR 7.6 [1.5–38.2], p = 0.02). We also identify factors associated with low response (last quartile; IgG7000AU/mL): age; previous SARS-CoV-2 infection and active Cancer. From this experience, we propose a strategy integrating anti-spike IgG monitoring to guide revaccination and dialysis center management in pandemic times. |
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Data from the medical field are thus mandatory. We report our experience with a BNT162b2-mRNA vaccine in a retrospective analysis of 241 dialysis patients including 193 who underwent anti-Spike-Protein-Receptor-Binding-Domain (RBD) IgG analysis. We show that a pro-active vaccine campaign is effective in convincing most patients to be vaccinated (95%) and frequently elicits a specific antibody response (94.3% after two doses and 98.4% after three doses). Only immunocompromised Status is associated with lack of seroconversion (OR 7.6 [1.5–38.2], p = 0.02). We also identify factors associated with low response (last quartile; IgG<500AU/mL): immunocompromised status, age, absence of RAAS inhibitors, low lymphocytes count, high C Reactive Protein; and with high response (high quartile; IgG>7000AU/mL): age; previous SARS-CoV-2 infection and active Cancer. From this experience, we propose a strategy integrating anti-spike IgG monitoring to guide revaccination and dialysis center management in pandemic times.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0257646</identifier><identifier>PMID: 34610031</identifier><language>eng</language><publisher>San Francisco: Public Library of Science</publisher><subject>Antibodies ; Antibody response ; Antigens ; Biology and life sciences ; C-reactive protein ; Care and treatment ; Complications and side effects ; COVID-19 ; Data collection ; Dialysis ; Drug dosages ; Health risks ; Hemodialysis ; Hemodialysis patients ; Immune response ; Immune response (humoral) ; Immune system ; Immunoglobulin G ; Infections ; Kidney diseases ; Lymphocytes ; Medicine and health sciences ; Monitoring ; mRNA ; mRNA vaccines ; Multivariate analysis ; Pandemics ; Patients ; Proteins ; Risk factors ; Seroconversion ; Severe acute respiratory syndrome ; Severe acute respiratory syndrome coronavirus 2 ; Telemedicine ; Transplants & implants ; Vaccines ; Viral diseases</subject><ispartof>PloS one, 2021-10, Vol.16 (10), p.e0257646-e0257646</ispartof><rights>COPYRIGHT 2021 Public Library of Science</rights><rights>2021 BACHELET et al. 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Data from the medical field are thus mandatory. We report our experience with a BNT162b2-mRNA vaccine in a retrospective analysis of 241 dialysis patients including 193 who underwent anti-Spike-Protein-Receptor-Binding-Domain (RBD) IgG analysis. We show that a pro-active vaccine campaign is effective in convincing most patients to be vaccinated (95%) and frequently elicits a specific antibody response (94.3% after two doses and 98.4% after three doses). Only immunocompromised Status is associated with lack of seroconversion (OR 7.6 [1.5–38.2], p = 0.02). We also identify factors associated with low response (last quartile; IgG<500AU/mL): immunocompromised status, age, absence of RAAS inhibitors, low lymphocytes count, high C Reactive Protein; and with high response (high quartile; IgG>7000AU/mL): age; previous SARS-CoV-2 infection and active Cancer. 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response after SARS-CoV-2 mRNA vaccines in dialysis patients: Integrating anti-SARS-CoV-2 Spike-Protein-RBD antibody monitoring to manage dialysis centers in pandemic times</title><author>Bachelet, Thomas ; Bourdenx, Jean-Philippe ; Martinez, Charlie ; Mucha, Simon ; Martin-Dupont, Philippe ; Perier, Valerie ; Pommereau, Antoine</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c735t-289915a4d18051282aa3f8bc36b46de34db421e0403df701244fd0fda92ace4c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Antibodies</topic><topic>Antibody response</topic><topic>Antigens</topic><topic>Biology and life sciences</topic><topic>C-reactive protein</topic><topic>Care and treatment</topic><topic>Complications and side effects</topic><topic>COVID-19</topic><topic>Data collection</topic><topic>Dialysis</topic><topic>Drug dosages</topic><topic>Health risks</topic><topic>Hemodialysis</topic><topic>Hemodialysis patients</topic><topic>Immune response</topic><topic>Immune response (humoral)</topic><topic>Immune system</topic><topic>Immunoglobulin G</topic><topic>Infections</topic><topic>Kidney diseases</topic><topic>Lymphocytes</topic><topic>Medicine and health sciences</topic><topic>Monitoring</topic><topic>mRNA</topic><topic>mRNA vaccines</topic><topic>Multivariate analysis</topic><topic>Pandemics</topic><topic>Patients</topic><topic>Proteins</topic><topic>Risk factors</topic><topic>Seroconversion</topic><topic>Severe acute respiratory syndrome</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>Telemedicine</topic><topic>Transplants & implants</topic><topic>Vaccines</topic><topic>Viral diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bachelet, Thomas</creatorcontrib><creatorcontrib>Bourdenx, Jean-Philippe</creatorcontrib><creatorcontrib>Martinez, 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Valerie</au><au>Pommereau, Antoine</au><au>Ito, Etsuro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Humoral response after SARS-CoV-2 mRNA vaccines in dialysis patients: Integrating anti-SARS-CoV-2 Spike-Protein-RBD antibody monitoring to manage dialysis centers in pandemic times</atitle><jtitle>PloS one</jtitle><date>2021-10-05</date><risdate>2021</risdate><volume>16</volume><issue>10</issue><spage>e0257646</spage><epage>e0257646</epage><pages>e0257646-e0257646</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Dialysis patients are both the most likely to benefit from vaccine protection against SARS-CoV-2 and at the highest risk of not developing an immune response. Data from the medical field are thus mandatory. We report our experience with a BNT162b2-mRNA vaccine in a retrospective analysis of 241 dialysis patients including 193 who underwent anti-Spike-Protein-Receptor-Binding-Domain (RBD) IgG analysis. We show that a pro-active vaccine campaign is effective in convincing most patients to be vaccinated (95%) and frequently elicits a specific antibody response (94.3% after two doses and 98.4% after three doses). Only immunocompromised Status is associated with lack of seroconversion (OR 7.6 [1.5–38.2], p = 0.02). We also identify factors associated with low response (last quartile; IgG<500AU/mL): immunocompromised status, age, absence of RAAS inhibitors, low lymphocytes count, high C Reactive Protein; and with high response (high quartile; IgG>7000AU/mL): age; previous SARS-CoV-2 infection and active Cancer. From this experience, we propose a strategy integrating anti-spike IgG monitoring to guide revaccination and dialysis center management in pandemic times.</abstract><cop>San Francisco</cop><pub>Public Library of Science</pub><pmid>34610031</pmid><doi>10.1371/journal.pone.0257646</doi><tpages>e0257646</tpages><orcidid>https://orcid.org/0000-0002-3273-1444</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antibodies Antibody response Antigens Biology and life sciences C-reactive protein Care and treatment Complications and side effects COVID-19 Data collection Dialysis Drug dosages Health risks Hemodialysis Hemodialysis patients Immune response Immune response (humoral) Immune system Immunoglobulin G Infections Kidney diseases Lymphocytes Medicine and health sciences Monitoring mRNA mRNA vaccines Multivariate analysis Pandemics Patients Proteins Risk factors Seroconversion Severe acute respiratory syndrome Severe acute respiratory syndrome coronavirus 2 Telemedicine Transplants & implants Vaccines Viral diseases |
title | Humoral response after SARS-CoV-2 mRNA vaccines in dialysis patients: Integrating anti-SARS-CoV-2 Spike-Protein-RBD antibody monitoring to manage dialysis centers in pandemic times |
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