Volume 46, Issue 2 pp. 244-249

Recurrent acute hemolytic transfusion reactions by antibodies against Doa antigens, not detected by cross-matching

Ruben Baumgarten

Ruben Baumgarten

From the Department of Clinical Chemistry & Hematology, Atrium Medical Center, Heerlen; the Department of Clinical Chemistry & Hematology, Albert Schweitzer Hospital, Dordrecht, the Netherlands; and the Sanquin Blood Bank Southwest Region, Rotterdam, the Netherlands.

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Warry Van Gelder

Warry Van Gelder

From the Department of Clinical Chemistry & Hematology, Atrium Medical Center, Heerlen; the Department of Clinical Chemistry & Hematology, Albert Schweitzer Hospital, Dordrecht, the Netherlands; and the Sanquin Blood Bank Southwest Region, Rotterdam, the Netherlands.

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Joyce Van Wintershoven

Joyce Van Wintershoven

From the Department of Clinical Chemistry & Hematology, Atrium Medical Center, Heerlen; the Department of Clinical Chemistry & Hematology, Albert Schweitzer Hospital, Dordrecht, the Netherlands; and the Sanquin Blood Bank Southwest Region, Rotterdam, the Netherlands.

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Petra A. Maaskant-Van Wijk

Petra A. Maaskant-Van Wijk

From the Department of Clinical Chemistry & Hematology, Atrium Medical Center, Heerlen; the Department of Clinical Chemistry & Hematology, Albert Schweitzer Hospital, Dordrecht, the Netherlands; and the Sanquin Blood Bank Southwest Region, Rotterdam, the Netherlands.

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Erik A.M. Beckers

Corresponding Author

Erik A.M. Beckers

From the Department of Clinical Chemistry & Hematology, Atrium Medical Center, Heerlen; the Department of Clinical Chemistry & Hematology, Albert Schweitzer Hospital, Dordrecht, the Netherlands; and the Sanquin Blood Bank Southwest Region, Rotterdam, the Netherlands.

E.A.M. Beckers, MD, PhD, Sanquin Blood Bank Southwest Region, Wytemaweg 10, 3015 CN Rotterdam, the Netherlands; e-mail: [email protected].Search for more papers by this author
First published: 02 December 2005
Citations: 13

Abstract

An 81-year-old male patient suffered from recurrent acute hemolytic transfusion reactions after transfusion with phenotyped cross-match-negative red blood cells (RBCs). Extensive posttransfusion workup eventually revealed Dombrock (a) (Doa) antibodies. Because commercially available cell panels do not allow for identification of anti-Doa and owing to the lack of Doa typing serum samples, selection of matched units of RBCs is dependent on negative cross-match results. In this case, selection of Do(a–) units by cross-matching failed, indicating that serologic methods were not reliable. A polymerase chain reaction with sequence-specific priming assay was used to detect DOA and DOB alleles, which encode Doa and Dob antigens, respectively. The patient was confirmed to be DOB/DOB by DNA sequencing. Furthermore, the involved mismatched units in each of the three hemolytic episodes were shown to be Do(a+). In the presenting case, DNA typing appeared to be superior to serologic methods in selecting matched RBC units in the presence of anti-Doa.

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