Human neutrophil antigen 3 genotype impacts neutrophil-mediated endothelial cell cytotoxicity in a two-event model of TRALI

Chiaretti S, Burton M, Hassel P, Radenkovic F, Devikashri N, Sultana AJ, Temple FT, Dean MM, Tung JP Blood Transfus DOI: 10.2450/2022.0013-22

Background: Antibodies against human neutrophil antigen (HNA)-3a are associated with severe cases of transfusion-related acute lung injury (TRALI). The HNA-3 system is located on choline transporter-like 2 (CTL-2) protein. CTL-2 is encoded by the gene SLC44A2 and a single-nucleotide polymorphism c.461G>A results in two antigens: HNA-3a and HNA-3b. Three HNA-3 genotypes/phenotypes exist: HNA-3aa, HNA-3bb, and HNA-3ab. Two different pathways of anti-HNA-3a TRALI have been described: a two-hit neutrophil-dependent pathway and a one-hit neutrophil-independent pathway. However, it is not clear whether HNA-3ab heterozygous patients have a lower risk of anti-HNA-3a-mediated TRALI compared to HNA-3aa homozygous patients.

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Bilateral Femoral Cannulation is associated with reduced Severe Limb Ischemia-related complications compared with Unilateral Femoral Cannulation in Adult Peripheral Venoarterial ECMO

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Letter to the Editor: Naming and Unnaming in the Extracorporeal Membrane Oxygenation Literature