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SARS‐COV‐2 vaccination with BNT162B2 in renal transplant patients: Risk factors for impaired response and immunological implications
Solid organ transplant patients are at a higher risk for poor CoronaVirus Disease‐2019 (COVID‐19)‐related outcomes and have been included as a priority group in the vaccination strategy worldwide. We assessed the safety and efficacy of a two‐dose vaccination cycle with mRNA‐based COVID‐19 vaccine (B...
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Published in: | Clinical Transplantation 2022-01, Vol.36 (1), p.e14495-n/a |
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description | Solid organ transplant patients are at a higher risk for poor CoronaVirus Disease‐2019 (COVID‐19)‐related outcomes and have been included as a priority group in the vaccination strategy worldwide. We assessed the safety and efficacy of a two‐dose vaccination cycle with mRNA‐based COVID‐19 vaccine (BNT162b2) among 82 kidney transplant outpatients followed in our center in Rome, Italy. After a median of 43 post‐vaccine days, a SARS‐CoV‐2 anti‐Spike seroprevalence of 52.4% (n = 43/82) was observed. No impact of the vaccination on antibody‐mediated rejection or graft function was observed, and no significant safety concerns were reported. Moreover, no de novo HLA‐donor‐specific antibodies (DSA) were detected during the follow‐up period. Only one patient with pre‐vaccination HLA‐DSA did not experience an increased intensity of the existing HLA‐DSA. During the follow‐up, only one infection (mild COVID‐19) was observed in a patient after receiving the first vaccine dose. According to the multivariable logistic regression analysis, lack of seroconversion after two‐dose vaccination independently associated with patient age ≥60 years (OR = 4.50; P = .02) and use of anti‐metabolite as an immunosuppressant drug (OR = 5.26; P = .004). Among younger patients not taking anti‐metabolites, the seroconversion rate was high (92.9%). Further larger studies are needed to assess the best COVID‐19 vaccination strategy in transplanted patients. |
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We assessed the safety and efficacy of a two‐dose vaccination cycle with mRNA‐based COVID‐19 vaccine (BNT162b2) among 82 kidney transplant outpatients followed in our center in Rome, Italy. After a median of 43 post‐vaccine days, a SARS‐CoV‐2 anti‐Spike seroprevalence of 52.4% (n = 43/82) was observed. No impact of the vaccination on antibody‐mediated rejection or graft function was observed, and no significant safety concerns were reported. Moreover, no de novo HLA‐donor‐specific antibodies (DSA) were detected during the follow‐up period. Only one patient with pre‐vaccination HLA‐DSA did not experience an increased intensity of the existing HLA‐DSA. During the follow‐up, only one infection (mild COVID‐19) was observed in a patient after receiving the first vaccine dose. According to the multivariable logistic regression analysis, lack of seroconversion after two‐dose vaccination independently associated with patient age ≥60 years (OR = 4.50; P = .02) and use of anti‐metabolite as an immunosuppressant drug (OR = 5.26; P = .004). Among younger patients not taking anti‐metabolites, the seroconversion rate was high (92.9%). Further larger studies are needed to assess the best COVID‐19 vaccination strategy in transplanted patients.</description><identifier>ISSN: 0902-0063</identifier><identifier>ISSN: 1399-0012</identifier><identifier>EISSN: 1399-0012</identifier><identifier>DOI: 10.1111/ctr.14495</identifier><identifier>PMID: 34569101</identifier><language>eng</language><publisher>Denmark: John Wiley & Sons, Inc</publisher><subject>Antibodies, Viral ; BNT162 Vaccine ; BNT162b2 vaccine ; COVID-19 ; COVID-19 Vaccines ; graft rejection ; HLA‐DSA ; Humans ; Kidney Transplantation ; Middle Aged ; Original ; Risk Factors ; SARS-CoV-2 ; Seroepidemiologic Studies ; solid organ transplant patients ; Vaccination</subject><ispartof>Clinical Transplantation, 2022-01, Vol.36 (1), p.e14495-n/a</ispartof><rights>2021 The Authors. published by John Wiley & Sons Ltd.</rights><rights>2021 The Authors. Clinical Transplantation published by John Wiley & Sons Ltd.</rights><rights>2021. 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We assessed the safety and efficacy of a two‐dose vaccination cycle with mRNA‐based COVID‐19 vaccine (BNT162b2) among 82 kidney transplant outpatients followed in our center in Rome, Italy. After a median of 43 post‐vaccine days, a SARS‐CoV‐2 anti‐Spike seroprevalence of 52.4% (n = 43/82) was observed. No impact of the vaccination on antibody‐mediated rejection or graft function was observed, and no significant safety concerns were reported. Moreover, no de novo HLA‐donor‐specific antibodies (DSA) were detected during the follow‐up period. Only one patient with pre‐vaccination HLA‐DSA did not experience an increased intensity of the existing HLA‐DSA. During the follow‐up, only one infection (mild COVID‐19) was observed in a patient after receiving the first vaccine dose. According to the multivariable logistic regression analysis, lack of seroconversion after two‐dose vaccination independently associated with patient age ≥60 years (OR = 4.50; P = .02) and use of anti‐metabolite as an immunosuppressant drug (OR = 5.26; P = .004). Among younger patients not taking anti‐metabolites, the seroconversion rate was high (92.9%). Further larger studies are needed to assess the best COVID‐19 vaccination strategy in transplanted patients.</description><subject>Antibodies, Viral</subject><subject>BNT162 Vaccine</subject><subject>BNT162b2 vaccine</subject><subject>COVID-19</subject><subject>COVID-19 Vaccines</subject><subject>graft rejection</subject><subject>HLA‐DSA</subject><subject>Humans</subject><subject>Kidney Transplantation</subject><subject>Middle Aged</subject><subject>Original</subject><subject>Risk Factors</subject><subject>SARS-CoV-2</subject><subject>Seroepidemiologic Studies</subject><subject>solid organ transplant patients</subject><subject>Vaccination</subject><issn>0902-0063</issn><issn>1399-0012</issn><issn>1399-0012</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>COVID</sourceid><recordid>eNp1kc9u1DAQxi0EokvhwAsgS1zgsK3t2E7MoVK7Kn-kikrbhavldezWJbGDnbTqrUeOPCNPwixbKkDCB3s085vPo_kQek7JHoWzb8e8RzlX4gGa0UqpOSGUPUQzogiDWFY76Ekpl5CVVIrHaKfiQipK6Ax9Oztcnv24_b44_Qw3w1fG2hDNGFLE12G8wEcfV1SyI4ZDxNlF0-Exm1iGzsQRDwC6OJY3eBnKF-yNHVMu2KeMQz-YkF0LTWVIsThsYgvZfoqpS-fBghIwHQSbz8pT9Mibrrhnd-8u-vT2eLV4Pz85ffdhcXgyt5xXYt5yyQklklHf1K1aC0WMpMQzYdeeKiNI3TAvPCOM2KquWiuUt1AljWg59dUuOtjqDtO6d62F8bPp9JBDb_KNTibovysxXOjzdKUbySXjBARe3Qnk9HVyZdR9KNZ1sBCXpqKZaOq64pJyQF_-g16mKcMON1Rdk0appgLq9ZayOZWSnb8fhhK98VeDv_qXv8C--HP6e_K3oQDsb4Hr0Lmb_yvpxWq5lfwJyIex4A</recordid><startdate>202201</startdate><enddate>202201</enddate><creator>Russo, Gianluca</creator><creator>Lai, Quirino</creator><creator>Poli, Luca</creator><creator>Perrone, Maria Paola</creator><creator>Gaeta, Aurelia</creator><creator>Rossi, Massimo</creator><creator>Mastroianni, Claudio M.</creator><creator>Garofalo, Manuela</creator><creator>Pretagostini, Renzo</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</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>COVID</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-8764-7389</orcidid><orcidid>https://orcid.org/0000-0003-1487-3235</orcidid></search><sort><creationdate>202201</creationdate><title>SARS‐COV‐2 vaccination with BNT162B2 in renal transplant patients: Risk factors for impaired response and immunological implications</title><author>Russo, Gianluca ; Lai, Quirino ; Poli, Luca ; Perrone, Maria Paola ; Gaeta, Aurelia ; Rossi, Massimo ; Mastroianni, Claudio M. ; Garofalo, Manuela ; Pretagostini, Renzo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4435-d464010621f87d9b590a610f25cbf19a50782f5f2020c373dc59fc25c085d41f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Antibodies, Viral</topic><topic>BNT162 Vaccine</topic><topic>BNT162b2 vaccine</topic><topic>COVID-19</topic><topic>COVID-19 Vaccines</topic><topic>graft rejection</topic><topic>HLA‐DSA</topic><topic>Humans</topic><topic>Kidney Transplantation</topic><topic>Middle Aged</topic><topic>Original</topic><topic>Risk Factors</topic><topic>SARS-CoV-2</topic><topic>Seroepidemiologic Studies</topic><topic>solid organ transplant patients</topic><topic>Vaccination</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Russo, Gianluca</creatorcontrib><creatorcontrib>Lai, Quirino</creatorcontrib><creatorcontrib>Poli, Luca</creatorcontrib><creatorcontrib>Perrone, Maria Paola</creatorcontrib><creatorcontrib>Gaeta, Aurelia</creatorcontrib><creatorcontrib>Rossi, Massimo</creatorcontrib><creatorcontrib>Mastroianni, Claudio M.</creatorcontrib><creatorcontrib>Garofalo, Manuela</creatorcontrib><creatorcontrib>Pretagostini, Renzo</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Online Library 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>Coronavirus Research Database</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical Transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Russo, Gianluca</au><au>Lai, Quirino</au><au>Poli, Luca</au><au>Perrone, Maria Paola</au><au>Gaeta, Aurelia</au><au>Rossi, Massimo</au><au>Mastroianni, Claudio M.</au><au>Garofalo, Manuela</au><au>Pretagostini, Renzo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>SARS‐COV‐2 vaccination with BNT162B2 in renal transplant patients: Risk factors for impaired response and immunological implications</atitle><jtitle>Clinical Transplantation</jtitle><addtitle>Clin Transplant</addtitle><date>2022-01</date><risdate>2022</risdate><volume>36</volume><issue>1</issue><spage>e14495</spage><epage>n/a</epage><pages>e14495-n/a</pages><issn>0902-0063</issn><issn>1399-0012</issn><eissn>1399-0012</eissn><abstract>Solid organ transplant patients are at a higher risk for poor CoronaVirus Disease‐2019 (COVID‐19)‐related outcomes and have been included as a priority group in the vaccination strategy worldwide. We assessed the safety and efficacy of a two‐dose vaccination cycle with mRNA‐based COVID‐19 vaccine (BNT162b2) among 82 kidney transplant outpatients followed in our center in Rome, Italy. After a median of 43 post‐vaccine days, a SARS‐CoV‐2 anti‐Spike seroprevalence of 52.4% (n = 43/82) was observed. No impact of the vaccination on antibody‐mediated rejection or graft function was observed, and no significant safety concerns were reported. Moreover, no de novo HLA‐donor‐specific antibodies (DSA) were detected during the follow‐up period. Only one patient with pre‐vaccination HLA‐DSA did not experience an increased intensity of the existing HLA‐DSA. During the follow‐up, only one infection (mild COVID‐19) was observed in a patient after receiving the first vaccine dose. According to the multivariable logistic regression analysis, lack of seroconversion after two‐dose vaccination independently associated with patient age ≥60 years (OR = 4.50; P = .02) and use of anti‐metabolite as an immunosuppressant drug (OR = 5.26; P = .004). Among younger patients not taking anti‐metabolites, the seroconversion rate was high (92.9%). Further larger studies are needed to assess the best COVID‐19 vaccination strategy in transplanted patients.</abstract><cop>Denmark</cop><pub>John Wiley & Sons, Inc</pub><pmid>34569101</pmid><doi>10.1111/ctr.14495</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-8764-7389</orcidid><orcidid>https://orcid.org/0000-0003-1487-3235</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antibodies, Viral BNT162 Vaccine BNT162b2 vaccine COVID-19 COVID-19 Vaccines graft rejection HLA‐DSA Humans Kidney Transplantation Middle Aged Original Risk Factors SARS-CoV-2 Seroepidemiologic Studies solid organ transplant patients Vaccination |
title | SARS‐COV‐2 vaccination with BNT162B2 in renal transplant patients: Risk factors for impaired response and immunological implications |
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