Association between renal failure and red blood cell alloimmunization among newly transfused patients

Background Renal failure and renal replacement therapy (RRT) affect the immune system and could therefore modulate red blood cell (RBC) alloimmunization after transfusion. Study Design and Methods We performed a nationwide multicenter case‐control study within a source population of newly transfused...

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Veröffentlicht in:Transfusion (Philadelphia, Pa.) Pa.), 2021-01, Vol.61 (1), p.35-41
Hauptverfasser: Oud, Josine A., Evers, Dorothea, Middelburg, Rutger A., Vooght, Karen M. K., Kerkhof, Daan, Visser, Otto, Péquériaux, Nathalie C.V., Hudig, Francisca, Bom, Johanna G., Zwaginga, Jaap Jan
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container_end_page 41
container_issue 1
container_start_page 35
container_title Transfusion (Philadelphia, Pa.)
container_volume 61
creator Oud, Josine A.
Evers, Dorothea
Middelburg, Rutger A.
Vooght, Karen M. K.
Kerkhof, Daan
Visser, Otto
Péquériaux, Nathalie C.V.
Hudig, Francisca
Bom, Johanna G.
Zwaginga, Jaap Jan
description Background Renal failure and renal replacement therapy (RRT) affect the immune system and could therefore modulate red blood cell (RBC) alloimmunization after transfusion. Study Design and Methods We performed a nationwide multicenter case‐control study within a source population of newly transfused patients between 2005 and 2015. Using conditional multivariate logistic regression, we compared first‐time transfusion‐induced RBC alloantibody formers (N = 505) with two nonalloimmunized recipients with similar transfusion burden (N = 1010). Results Renal failure was observed in 17% of the control and 13% of the case patients. A total of 41% of the control patients and 34% of case patients underwent acute RRT. Renal failure without RRT was associated with lower alloimmunization risks after blood transfusion (moderate renal failure: adjusted relative rate [RR], 0.82 [95% confidence interval (CI), 0.67‐1.01]); severe renal failure, adjusted RR, 0.76 [95% CI, 0.55‐1.05]). With severe renal failure patients mainly receiving RRT, the lowest alloimmunization risk was found in particularly these patients [adjusted RR 0.48 (95% CI 0.39‐0.58)]. This was similar for patients receiving RRT for acute or chronic renal failure (adjusted RR, 0.59 [95% CI, 0.46‐0.75]); and adjusted RR, 0.62 [95% CI 0.45‐0.88], respectively). Conclusion These findings are indicative of a weakened humoral response in acute as well as chronic renal failure, which appeared to be most pronounced when treated with RRT. Future research should focus on how renal failure and RRT mechanistically modulate RBC alloimmunization.
doi_str_mv 10.1111/trf.16166
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K. ; Kerkhof, Daan ; Visser, Otto ; Péquériaux, Nathalie C.V. ; Hudig, Francisca ; Bom, Johanna G. ; Zwaginga, Jaap Jan</creator><creatorcontrib>Oud, Josine A. ; Evers, Dorothea ; Middelburg, Rutger A. ; Vooght, Karen M. K. ; Kerkhof, Daan ; Visser, Otto ; Péquériaux, Nathalie C.V. ; Hudig, Francisca ; Bom, Johanna G. ; Zwaginga, Jaap Jan</creatorcontrib><description>Background Renal failure and renal replacement therapy (RRT) affect the immune system and could therefore modulate red blood cell (RBC) alloimmunization after transfusion. Study Design and Methods We performed a nationwide multicenter case‐control study within a source population of newly transfused patients between 2005 and 2015. Using conditional multivariate logistic regression, we compared first‐time transfusion‐induced RBC alloantibody formers (N = 505) with two nonalloimmunized recipients with similar transfusion burden (N = 1010). Results Renal failure was observed in 17% of the control and 13% of the case patients. A total of 41% of the control patients and 34% of case patients underwent acute RRT. Renal failure without RRT was associated with lower alloimmunization risks after blood transfusion (moderate renal failure: adjusted relative rate [RR], 0.82 [95% confidence interval (CI), 0.67‐1.01]); severe renal failure, adjusted RR, 0.76 [95% CI, 0.55‐1.05]). With severe renal failure patients mainly receiving RRT, the lowest alloimmunization risk was found in particularly these patients [adjusted RR 0.48 (95% CI 0.39‐0.58)]. This was similar for patients receiving RRT for acute or chronic renal failure (adjusted RR, 0.59 [95% CI, 0.46‐0.75]); and adjusted RR, 0.62 [95% CI 0.45‐0.88], respectively). Conclusion These findings are indicative of a weakened humoral response in acute as well as chronic renal failure, which appeared to be most pronounced when treated with RRT. Future research should focus on how renal failure and RRT mechanistically modulate RBC alloimmunization.</description><identifier>ISSN: 0041-1132</identifier><identifier>EISSN: 1537-2995</identifier><identifier>DOI: 10.1111/trf.16166</identifier><identifier>PMID: 33295653</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley &amp; Sons, Inc</publisher><subject>Alloantibodies ; Blood ; Blood transfusion ; Confidence intervals ; dialysis ; Erythrocytes ; Failure ; Immune response (humoral) ; Immune system ; Isoimmunization ; Kidneys ; Population studies ; red blood cell alloimmunization ; Renal failure ; renal replacement therapy ; Statistical analysis ; Transfusion ; Transfusion Medicine</subject><ispartof>Transfusion (Philadelphia, Pa.), 2021-01, Vol.61 (1), p.35-41</ispartof><rights>2020 The Authors. published by Wiley Periodicals LLC. on behalf of AABB.</rights><rights>2020 The Authors. Transfusion published by Wiley Periodicals LLC. on behalf of AABB.</rights><rights>2020. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4436-49e7a44cc88e8880e35400150f378412e41a303ae41b05d09d5223a1cca897873</citedby><cites>FETCH-LOGICAL-c4436-49e7a44cc88e8880e35400150f378412e41a303ae41b05d09d5223a1cca897873</cites><orcidid>0000-0002-8985-6627</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Ftrf.16166$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Ftrf.16166$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33295653$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Oud, Josine A.</creatorcontrib><creatorcontrib>Evers, Dorothea</creatorcontrib><creatorcontrib>Middelburg, Rutger A.</creatorcontrib><creatorcontrib>Vooght, Karen M. K.</creatorcontrib><creatorcontrib>Kerkhof, Daan</creatorcontrib><creatorcontrib>Visser, Otto</creatorcontrib><creatorcontrib>Péquériaux, Nathalie C.V.</creatorcontrib><creatorcontrib>Hudig, Francisca</creatorcontrib><creatorcontrib>Bom, Johanna G.</creatorcontrib><creatorcontrib>Zwaginga, Jaap Jan</creatorcontrib><title>Association between renal failure and red blood cell alloimmunization among newly transfused patients</title><title>Transfusion (Philadelphia, Pa.)</title><addtitle>Transfusion</addtitle><description>Background Renal failure and renal replacement therapy (RRT) affect the immune system and could therefore modulate red blood cell (RBC) alloimmunization after transfusion. Study Design and Methods We performed a nationwide multicenter case‐control study within a source population of newly transfused patients between 2005 and 2015. Using conditional multivariate logistic regression, we compared first‐time transfusion‐induced RBC alloantibody formers (N = 505) with two nonalloimmunized recipients with similar transfusion burden (N = 1010). Results Renal failure was observed in 17% of the control and 13% of the case patients. A total of 41% of the control patients and 34% of case patients underwent acute RRT. Renal failure without RRT was associated with lower alloimmunization risks after blood transfusion (moderate renal failure: adjusted relative rate [RR], 0.82 [95% confidence interval (CI), 0.67‐1.01]); severe renal failure, adjusted RR, 0.76 [95% CI, 0.55‐1.05]). With severe renal failure patients mainly receiving RRT, the lowest alloimmunization risk was found in particularly these patients [adjusted RR 0.48 (95% CI 0.39‐0.58)]. This was similar for patients receiving RRT for acute or chronic renal failure (adjusted RR, 0.59 [95% CI, 0.46‐0.75]); and adjusted RR, 0.62 [95% CI 0.45‐0.88], respectively). Conclusion These findings are indicative of a weakened humoral response in acute as well as chronic renal failure, which appeared to be most pronounced when treated with RRT. 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K.</creator><creator>Kerkhof, Daan</creator><creator>Visser, Otto</creator><creator>Péquériaux, Nathalie C.V.</creator><creator>Hudig, Francisca</creator><creator>Bom, Johanna G.</creator><creator>Zwaginga, Jaap Jan</creator><general>John Wiley &amp; Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-8985-6627</orcidid></search><sort><creationdate>202101</creationdate><title>Association between renal failure and red blood cell alloimmunization among newly transfused patients</title><author>Oud, Josine A. ; Evers, Dorothea ; Middelburg, Rutger A. ; Vooght, Karen M. K. ; Kerkhof, Daan ; Visser, Otto ; Péquériaux, Nathalie C.V. ; Hudig, Francisca ; Bom, Johanna G. ; Zwaginga, Jaap Jan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4436-49e7a44cc88e8880e35400150f378412e41a303ae41b05d09d5223a1cca897873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Alloantibodies</topic><topic>Blood</topic><topic>Blood transfusion</topic><topic>Confidence intervals</topic><topic>dialysis</topic><topic>Erythrocytes</topic><topic>Failure</topic><topic>Immune response (humoral)</topic><topic>Immune system</topic><topic>Isoimmunization</topic><topic>Kidneys</topic><topic>Population studies</topic><topic>red blood cell alloimmunization</topic><topic>Renal failure</topic><topic>renal replacement therapy</topic><topic>Statistical analysis</topic><topic>Transfusion</topic><topic>Transfusion Medicine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oud, Josine A.</creatorcontrib><creatorcontrib>Evers, Dorothea</creatorcontrib><creatorcontrib>Middelburg, Rutger A.</creatorcontrib><creatorcontrib>Vooght, Karen M. K.</creatorcontrib><creatorcontrib>Kerkhof, Daan</creatorcontrib><creatorcontrib>Visser, Otto</creatorcontrib><creatorcontrib>Péquériaux, Nathalie C.V.</creatorcontrib><creatorcontrib>Hudig, Francisca</creatorcontrib><creatorcontrib>Bom, Johanna G.</creatorcontrib><creatorcontrib>Zwaginga, Jaap Jan</creatorcontrib><collection>Wiley-Blackwell Open Access Titles</collection><collection>Wiley Free Content</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Transfusion (Philadelphia, Pa.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oud, Josine A.</au><au>Evers, Dorothea</au><au>Middelburg, Rutger A.</au><au>Vooght, Karen M. K.</au><au>Kerkhof, Daan</au><au>Visser, Otto</au><au>Péquériaux, Nathalie C.V.</au><au>Hudig, Francisca</au><au>Bom, Johanna G.</au><au>Zwaginga, Jaap Jan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association between renal failure and red blood cell alloimmunization among newly transfused patients</atitle><jtitle>Transfusion (Philadelphia, Pa.)</jtitle><addtitle>Transfusion</addtitle><date>2021-01</date><risdate>2021</risdate><volume>61</volume><issue>1</issue><spage>35</spage><epage>41</epage><pages>35-41</pages><issn>0041-1132</issn><eissn>1537-2995</eissn><abstract>Background Renal failure and renal replacement therapy (RRT) affect the immune system and could therefore modulate red blood cell (RBC) alloimmunization after transfusion. Study Design and Methods We performed a nationwide multicenter case‐control study within a source population of newly transfused patients between 2005 and 2015. Using conditional multivariate logistic regression, we compared first‐time transfusion‐induced RBC alloantibody formers (N = 505) with two nonalloimmunized recipients with similar transfusion burden (N = 1010). Results Renal failure was observed in 17% of the control and 13% of the case patients. A total of 41% of the control patients and 34% of case patients underwent acute RRT. Renal failure without RRT was associated with lower alloimmunization risks after blood transfusion (moderate renal failure: adjusted relative rate [RR], 0.82 [95% confidence interval (CI), 0.67‐1.01]); severe renal failure, adjusted RR, 0.76 [95% CI, 0.55‐1.05]). With severe renal failure patients mainly receiving RRT, the lowest alloimmunization risk was found in particularly these patients [adjusted RR 0.48 (95% CI 0.39‐0.58)]. This was similar for patients receiving RRT for acute or chronic renal failure (adjusted RR, 0.59 [95% CI, 0.46‐0.75]); and adjusted RR, 0.62 [95% CI 0.45‐0.88], respectively). Conclusion These findings are indicative of a weakened humoral response in acute as well as chronic renal failure, which appeared to be most pronounced when treated with RRT. Future research should focus on how renal failure and RRT mechanistically modulate RBC alloimmunization.</abstract><cop>Hoboken, USA</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>33295653</pmid><doi>10.1111/trf.16166</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-8985-6627</orcidid><oa>free_for_read</oa></addata></record>
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source Wiley Online Library Journals Frontfile Complete
subjects Alloantibodies
Blood
Blood transfusion
Confidence intervals
dialysis
Erythrocytes
Failure
Immune response (humoral)
Immune system
Isoimmunization
Kidneys
Population studies
red blood cell alloimmunization
Renal failure
renal replacement therapy
Statistical analysis
Transfusion
Transfusion Medicine
title Association between renal failure and red blood cell alloimmunization among newly transfused patients
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