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Article

A simple, practical model for reducing alloimmunization in patients with sickle cell disease.

American journal of hematology - 1 Jun 1993

Sosler S D, Jilly B J, Saporito C, Koshy M

Abstract excerpt

Patients with sickle cell disease (SCD) form immune alloantibodies more frequently than other transfused populations because red cells (RBCs) from white donors (with a higher incidence of certain Rh, Duffy, Kell, and Kidd blood group antigens) are transfused to black patients often lacking these antigens. We propose a model to reduce alloimmunization in patients with SCD by providing them with blood from only...

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Share to Antibody Formation
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 8342535
DOI: 10.1002/ajh.2830430206

Genes

SCD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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A simple, practical model for reducing alloimmunization in patients with sickle cell disease.PMID 8342535Read ↗

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Medical and economic implications of strategies to prevent alloimmunization in sickle cell disease.Semantic proximity Read ↗

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Barriers to using molecularly typed minority red blood cell donors in support of chronically transfused adult patients with sickle cell disease.Semantic proximity Read ↗

Red Blood Cell Alloimmunization in Sickle Cell Disease: Listen to Your AncestorsSemantic proximity Read ↗

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