| Literature DB >> 25277423 |
Abstract
Platelet refractoriness is a serious complication for patients receiving recurrent platelet transfusions, which can be explained by non-immune and immune causes. Human Leukocyte Antigens (HLA) allo-immunization, especially against HLA class I, is the major cause for immune platelet refractoriness. To a lesser extent, allo-antibodies against specific Human Platelet Antigen (HPA) are also involved. Pregnancy, transplantation and previous transfusions can lead to allo-immune reaction against platelet antigens. After transfusion, platelet count is decreased by accelerated platelet destruction related to antibodies fixation on incompatible platelet antigens. New laboratory tests for allo-antibodies identification were developed to improve sensibility and specificity, especially with the LUMINEX(®) technology. The good use and interpretation of these antibodies assays can improve strategies for platelet refractoriness prevention and management with a patient adapted response. Compatible platelets units can be selected according to their identity with recipient typing or immune compatibility regarding HLA or HPA antibodies or HLA epitope compatibility. Prospective studies are needed to further confirm the clinical benefit of new allo-antibodies identification methods and consensus strategies for immune platelet refractoriness management.Entities:
Keywords: Allo-immunisation; Allo-immunization; Antibodies; Anticorps; Diagnosis; Diagnostic; HLA; HPA; Inefficacité plaquettaire; LUMINEX(®); Plaquettes; Platelet; Platelet refractoriness; Transfusion; État réfractaire
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Year: 2014 PMID: 25277423 DOI: 10.1016/j.tracli.2014.08.140
Source DB: PubMed Journal: Transfus Clin Biol ISSN: 1246-7820 Impact factor: 1.406