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The first case of severe acute hemolytic transfusion reaction caused by anti-Sc2.
Lemay, Anne-Sophie; Tong, Tik Nga; Branch, Donald R; Huang, Mary; Sumner, Christopher; Oldfield, Lynne; Hawes, Janice; Cserti-Gazdewich, Christine M; Lau, Wendy.
Affiliation
  • Lemay AS; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
  • Tong TN; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
  • Branch DR; the Centre for Innovation, Toronto, Ontario, Canada.
  • Huang M; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
  • Sumner C; the Centre for Innovation, Toronto, Ontario, Canada.
  • Oldfield L; University Health Network, Toronto, Ontario, Canada.
  • Hawes J; Diagnostic Services, Canadian Blood Services, Toronto, Ontario, Canada.
  • Cserti-Gazdewich CM; Diagnostic Services, Canadian Blood Services, Toronto, Ontario, Canada.
  • Lau W; Diagnostic Services, Canadian Blood Services, Toronto, Ontario, Canada.
Transfusion ; 58(11): 2506-2512, 2018 11.
Article in En | MEDLINE | ID: mdl-30299537
ABSTRACT

BACKGROUND:

Alloantibodies to the low-frequency antigen Scianna-2 (Sc2) have been implicated in cases of hemolytic disease of the fetus and newborn but never in hemolytic transfusion reactions (HTRs); thus, the clinical significance of anti-Sc2 has yet to be fully addressed. STUDY DESIGN AND

METHODS:

A 26-year-old woman with thalassemia presented rigors, fever, nausea, abdominal pain, and hemolytic biochemistry after exposure to 75 mL of plasma-reduced red blood cells (RBCs). The RBC unit was issued by electronic crossmatch but was 3+ incompatible on recrossmatch by gel indirect antiglobulin test (IAT). The patient had anti-Sc2 previously identified, but considered to be clinically insignificant. The transfusion history was reviewed and a monocyte monolayer assay (MMA) was performed.

RESULTS:

The patient was investigated for a RBC reaction 9 years prior, when she developed symptoms of HTR. The RBC unit was crossmatched by immediate spin due to consistent screen negativity. Full crossmatch found the RBC 1+ incompatible by gel IAT with both pre/post samples, while direct antiglobulin test was negative (pre) and 1+ immunoglobulin G positive (post). The antibody remained unidentified and she was committed to gel IAT crossmatch. Two-years later, the specificity to Sc2 was deduced when one RBC unit was found 3+ incompatible. Finally, the transfusion reaction reported herein occurred when she received by happenstance RBCs from the same donor who was associated with the remote reaction 9 years earlier. MMA yielded highly positive phagocytic indices only for Sc2+ RBCs, including the donor's RBCs that triggered the severe HTR.

CONCLUSION:

This is the first case of HTR caused by anti-Sc2 confirmed by clinical findings and MMA.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transfusion Reaction / Isoantibodies Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies Limits: Adult / Female / Humans Language: En Journal: Transfusion Year: 2018 Document type: Article Affiliation country: Canada

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transfusion Reaction / Isoantibodies Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies Limits: Adult / Female / Humans Language: En Journal: Transfusion Year: 2018 Document type: Article Affiliation country: Canada