The evanescence and persistence of RBC alloantibodies in blood donors.


Journal

Transfusion
ISSN: 1537-2995
Titre abrégé: Transfusion
Pays: United States
ID NLM: 0417360

Informations de publication

Date de publication:
04 2020
Historique:
received: 17 11 2019
revised: 30 01 2020
accepted: 30 01 2020
pubmed: 16 2 2020
medline: 9 9 2020
entrez: 16 2 2020
Statut: ppublish

Résumé

Blood donors represent a healthy population, whose red blood cell (RBC) alloantibody persistence or evanescence kinetics may differ from those of immunocompromised patients. A better understanding of the biologic factors impacting antibody persistence is warranted, as the presence of alloantibodies may impact donor health and the fate of the donated blood product. Donor/donation data collected from four US blood centers from 2012 to 2016 as part of the Recipient Epidemiology and Donor Evaluation Study-III (REDS-III) were analyzed. Clinically significant antibodies from blood donors with more than one donation who underwent at least one follow-up antibody screen after the initial antibody identification were included. Of 632,378 blood donors, 481 (128 males and 353 females) fit inclusion criteria. Antibody screens detected 562 alloantibodies, with 368 of 562 (65%) of antibodies being persistently detected and with 194 of 562 (35%) becoming evanescent. Factors associated with antibody persistence included antibody specificity, detection at the first donation, reported history of transfusion, and detection of multiple antibodies concurrently. Anti-D, C, and Fy These data provide insight into variables impacting the duration of antibody detection, and they may also influence blood donor center policies regarding donor recruitment/acceptance.

Sections du résumé

BACKGROUND
Blood donors represent a healthy population, whose red blood cell (RBC) alloantibody persistence or evanescence kinetics may differ from those of immunocompromised patients. A better understanding of the biologic factors impacting antibody persistence is warranted, as the presence of alloantibodies may impact donor health and the fate of the donated blood product.
METHODS
Donor/donation data collected from four US blood centers from 2012 to 2016 as part of the Recipient Epidemiology and Donor Evaluation Study-III (REDS-III) were analyzed. Clinically significant antibodies from blood donors with more than one donation who underwent at least one follow-up antibody screen after the initial antibody identification were included. Of 632,378 blood donors, 481 (128 males and 353 females) fit inclusion criteria.
RESULTS
Antibody screens detected 562 alloantibodies, with 368 of 562 (65%) of antibodies being persistently detected and with 194 of 562 (35%) becoming evanescent. Factors associated with antibody persistence included antibody specificity, detection at the first donation, reported history of transfusion, and detection of multiple antibodies concurrently. Anti-D, C, and Fy
CONCLUSIONS
These data provide insight into variables impacting the duration of antibody detection, and they may also influence blood donor center policies regarding donor recruitment/acceptance.

Identifiants

pubmed: 32061102
doi: 10.1111/trf.15718
doi:

Substances chimiques

Isoantibodies 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

831-839

Informations de copyright

© 2020 AABB.

Références

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Auteurs

Ronald G Hauser (RG)

Yale University, Department of Laboratory Medicine, New Haven, Connecticut.
Department of Pathology & Laboratory Medicine Service, Veterans Affairs Connecticut Healthcare System, West Haven, Connecticut.

Denise Esserman (D)

Department of Biostatistics, Yale School of Public Health, New Haven, Connecticut.

Matthew S Karafin (MS)

Versiti, Milwaukee, Wisconsin.
Department of Pathology & Laboratory Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.

Sylvia Tan (S)

RTI International, Rockville, Maryland.

Raisa Balbuena-Merle (R)

Yale University, Department of Laboratory Medicine, New Haven, Connecticut.
Department of Pathology & Laboratory Medicine Service, Veterans Affairs Connecticut Healthcare System, West Haven, Connecticut.

Bryan R Spencer (BR)

Yale University, Department of Laboratory Medicine, New Haven, Connecticut.
American Red Cross Scientific Affairs, Dedham, Massachusetts.

Nareg H Roubinian (NH)

Department of Laboratory Medicine, University of California, San Francisco, California.
Blood Systems Research Institute, San Francisco, California.

Yanyun Wu (Y)

Yale University, Department of Laboratory Medicine, New Haven, Connecticut.
Bloodworks Northwest, Seattle, Washington.

Darrell J Triulzi (DJ)

University of Pittsburgh and Vitalant, Pittsburgh, Pennsylvania.

Steve Kleinman (S)

Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.

Jerome L Gottschall (JL)

Versiti, Milwaukee, Wisconsin.
Department of Pathology & Laboratory Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.

Jeanne E Hendrickson (JE)

Yale University, Department of Laboratory Medicine, New Haven, Connecticut.
Department of Pediatrics, Yale University, New Haven, Connecticut.

Christopher A Tormey (CA)

Yale University, Department of Laboratory Medicine, New Haven, Connecticut.
Department of Pathology & Laboratory Medicine Service, Veterans Affairs Connecticut Healthcare System, West Haven, Connecticut.

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