<abstract xmlns="http://www.w3.org/1999/xhtml">An alloantibody to a high-incidence antigen, associated with multiple other alloantibodies, made it impossible to supply antigen-negative red blood cells (RBCs) for a chronically transfused sickle cell anemia patient. Anti-Cra, -E, -K, -S, -Fy”, -Fyb, as well as anti-M reactive at 37°C and in the antiglobulin phase of testing, were identified in the patient’s serum. An extensive search of rare donor files at the American Red Cross and at the American Association of Blood Banks (AABB) failed to identify Cr(a —), M–, E–, K –, S –, Fy(a – b –) donors. Various studies were performed to predict the clinical significance of the anti-Cra and anti-M. Results of 51chromium survival studies showed 91.8 percent survival at 10 minutes and 87.2 percent survival at 60 minutes with Cr(a +), M –, E –, K –, S –, Fy(a – b –) red cells, suggesting that immediate destruction of transfused Cr(a +) red cells would be unlikely. However, further analysis revealed diminished long-term survival of the donor’s red cells with only 60.1 percent recovery at six days (T 1/2 = 12 days) and 10.8 percent at 14 days (T 1/2 = 4.5 days). A monocyte-monolayer assay (MMA) indicated that both the anti-Cra (5.9%) and anti-M (18%) would probably be clinically significant (normal value 0 3%). Mass screening continues at several blood centers for Cr(a –),M — ,E-,K—,S—, Fy(a – b –) donors. However, if no suitable donors are found, the results of the 51chromium survival studies and the MMA support the decision to transfuse this patient with Cr(a +), M –, Fy(a–b–),S–,K–,E – red cells, if necessary.</abstract>

An alloantibody to a high-incidence antigen, associated with multiple other alloantibodies, made it impossible to supply antigen-negative red blood cells (RBCs) for a chronically transfused sickle cell anemia patient. Anti-Cra, -E, -K, -S, -Fy”, -Fyb, as well as anti-M reactive at 37°C and in the antiglobulin phase of testing, were identified in the patient’s serum. An extensive search of rare donor files at the American Red Cross and at the American Association of Blood Banks (AABB) failed to identify Cr(a —), M–, E–, K –, S –, Fy(a – b –) donors. Various studies were performed to predict the clinical significance of the anti-Cra and anti-M. Results of 51chromium survival studies showed 91.8 percent survival at 10 minutes and 87.2 percent survival at 60 minutes with Cr(a +), M –, E –, K –, S –, Fy(a – b –) red cells, suggesting that immediate destruction of transfused Cr(a +) red cells would be unlikely. However, further analysis revealed diminished long-term survival of the donor’s red cells with only 60.1 percent recovery at six days (T 1/2 = 12 days) and 10.8 percent at 14 days (T 1/2 = 4.5 days). A monocyte-monolayer assay (MMA) indicated that both the anti-Cra (5.9%) and anti-M (18%) would probably be clinically significant (normal value 0 3%). Mass screening continues at several blood centers for Cr(a –),M — ,E-,K—,S—, Fy(a – b –) donors. However, if no suitable donors are found, the results of the 51chromium survival studies and the MMA support the decision to transfuse this patient with Cr(a +), M –, Fy(a–b–),S–,K–,E – red cells, if necessary.

Assessing the clinical significance of anti-Cra and anti-M in a chronically transfused sickle cell patient

University Hospitals, Associate Professor

Immunohematology

Assessing the clinical significance of anti-Cr and anti-M in a chronically transfused sickle cell patient

An alloantibody to a high-incidence antigen, associated with multiple other alloantibodies, made it impossible to supply antigen-negative red blood cells...

Assessing the clinical significance of anti-Cr^a and anti-M in a chronically transfused sickle cell patient

Published Online: Dec 29, 2020

Page range: 71 - 74

DOI: https://doi.org/10.21307/immunohematology-2019-1108

© 1988 M.B. Leatherbarrow et al., published by Sciendo