A narrative review on progress and development of anti-CD36 antibody detection

Annals of blood Pub Date : 2021-01-01 DOI:10.21037/aob-21-48
Xiuzhang Xu, S. Santoso
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Abstract

Immune-mediated thrombocytopenia occurs due to alloantibodies against platelet antigens, such as the ABO blood group antigens, HLA class I, and human platelet antigens (HPA). In recent years, more than 30 HPA have been identified (https://www.versiti.org/medicalprofessionals/precision-medicine-expertise/plateletantigen-database/hpa-gene-database). Among them, alloantibodies against the HPA-1a formed by point mutation (Leu33Pro) on platelet glycoprotein (GP) IIIa (known as β3 integrin) are responsible for most cases of alloimmune thrombocytopenia in Caucasians (1). However, foetal and neonatal alloimmune thrombocytopenia (FNAIT) caused by anti-HPA-1a antibodies has not been well recognized in other populations. Interestingly, accumulating evidence indicates that immune-mediated thrombocytopenia caused Review Article
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综述了抗cd36抗体检测的研究进展
免疫介导的血小板减少症的发生是由于针对血小板抗原的同种抗体,如ABO血型抗原、HLA I类和人血小板抗原(HPA)。近年来,已经发现了30多种HPA (https://www.versiti.org/medicalprofessionals/precision-medicine-expertise/plateletantigen-database/hpa-gene-database)。其中,针对血小板糖蛋白(GP) IIIa(即β3整合素)上由点突变(Leu33Pro)形成的HPA-1a的同种异体抗体是导致高加索人中大多数同种异体免疫性血小板减少症的原因(1)。然而,在其他人群中,由抗HPA-1a抗体引起的胎儿和新生儿同种异体免疫性血小板减少症(FNAIT)尚未得到很好的认识。有趣的是,越来越多的证据表明免疫介导的血小板减少引起的
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