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本文引用的文献

1
Red blood cell alloimmunization mitigation strategies.红细胞同种免疫缓解策略。
Transfus Med Rev. 2014 Jul;28(3):137-44. doi: 10.1016/j.tmrv.2014.04.008. Epub 2014 May 15.
2
HLA-DRB1*07:01 allele is primarily associated with the Diego a alloimmunization in a Brazilian population.HLA-DRB1*07:01 等位基因主要与巴西人群中的 Diego a 同种免疫有关。
Transfusion. 2014 Oct;54(10):2468-76. doi: 10.1111/trf.12652. Epub 2014 Apr 14.
3
HLA-DRB1 associations in individuals with single and multiple clinically relevant red blood cell antibodies.具有单一和多种临床相关红细胞抗体个体中的HLA-DRB1关联
Transfusion. 2014 Aug;54(8):1971-80. doi: 10.1111/trf.12624. Epub 2014 Mar 24.
4
Systems analysis of sex differences reveals an immunosuppressive role for testosterone in the response to influenza vaccination.系统分析性别差异揭示了睾酮在流感疫苗接种反应中的免疫抑制作用。
Proc Natl Acad Sci U S A. 2014 Jan 14;111(2):869-74. doi: 10.1073/pnas.1321060111. Epub 2013 Dec 23.
5
Minor RBC Ab and allo-SCT.轻微红细胞抗体与异基因造血干细胞移植
Bone Marrow Transplant. 2014 Mar;49(3):456-7. doi: 10.1038/bmt.2013.196. Epub 2013 Dec 9.
6
The association of CD81 polymorphisms with alloimmunization in sickle cell disease.镰状细胞病中CD81基因多态性与同种免疫的关联
Clin Dev Immunol. 2013;2013:937846. doi: 10.1155/2013/937846. Epub 2013 May 22.
7
High prevalence of red blood cell alloimmunization in sickle cell disease despite transfusion from Rh-matched minority donors.尽管输注了来自 Rh 匹配的少数群体供者的血液,镰状细胞病患者仍存在红细胞同种免疫的高发率。
Blood. 2013 Aug 8;122(6):1062-71. doi: 10.1182/blood-2013-03-490623. Epub 2013 May 30.
8
Record fragmentation due to transfusion at multiple health care facilities: a risk factor for delayed hemolytic transfusion reactions.因在多家医疗机构输血导致的记录碎片:延迟性溶血性输血反应的一个风险因素。
Transfusion. 2014 Jan;54(1):98-103. doi: 10.1111/trf.12251. Epub 2013 May 27.
9
Neonatal alloimmunization: a rare case of multiple alloantibody formation in a patient with disseminated histoplasmosis.新生儿同种免疫:1例播散性组织胞浆菌病患者出现多种同种抗体形成的罕见病例。
Transfusion. 2013 May;53(5):1140-1. doi: 10.1111/trf.12132.
10
Alloimmunization screening after transfusion of red blood cells in a prospective study.一项前瞻性研究中红细胞输血后的同种免疫筛查。
Rev Bras Hematol Hemoter. 2012;34(3):206-11. doi: 10.5581/1516-8484.20120051.

临床和生物学因素对输血相关非 ABO 抗原同种免疫的影响:应答者、高应答者和无应答者。

The Influence of Clinical and Biological Factors on Transfusion-Associated Non-ABO Antigen Alloimmunization: Responders, Hyper-Responders, and Non-Responders.

机构信息

Department of Laboratory Medicine, Yale University School of Medicine, New Haven, CT, USA.

Department of Laboratory Medicine, Yale University School of Medicine, New Haven, CT, USA ; Pathology & Laboratory Medicine Service, VA Connecticut Healthcare System, West Haven, CT, USA.

出版信息

Transfus Med Hemother. 2014 Nov;41(6):420-9. doi: 10.1159/000369109. Epub 2014 Nov 17.

DOI:10.1159/000369109
PMID:25670929
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4280450/
Abstract

In the context of transfusion medicine, alloimmunization most often refers to the development of antibodies to non-ABO red blood cell (RBC) antigens following pregnancy, transfusion, or transplantation. The development of RBC alloantibodies can have important clinical consequences, particularly in patients who require chronic transfusions. It has been suggested that alloimmunization is more common in some clinical circumstances and patient populations than in others. As such, individuals that develop alloantibodies are frequently referred to as 'responders' in the medical literature. In contrast, individuals that do not develop alloantibodies despite repeated exposures to non-self blood group antigens have been referred to as 'non-responders'. The purpose of this article is to review the phenomenon of RBC alloimmunization in the context of responders and non-responders to: i) establish a basic framework for alloimmunization as reported across several diverse patient populations; ii) more fully explore literature reports which support the concept of responders/non-responders regarding blood group antigen alloimmunization; iii) summarize the mechanisms that have been shown to predispose an individual to alloimmunization to determine how these factors may differentiate 'responders' from 'non-responders'; and iv) briefly discuss some practical approaches to prevent alloimmunization in patients who may be prone to alloantibody development.

摘要

在输血医学中,同种免疫通常是指妊娠、输血或移植后针对非 ABO 红细胞(RBC)抗原产生抗体。RBC 同种抗体的产生可能会产生重要的临床后果,特别是在需要长期输血的患者中。有研究表明,同种免疫在某些临床情况下和患者人群中比在其他情况下更为常见。因此,在医学文献中,产生同种抗体的个体通常被称为“应答者”。相比之下,尽管反复接触非自身血型抗原,但未产生同种抗体的个体被称为“无应答者”。本文的目的是在应答者和无应答者的背景下,回顾 RBC 同种免疫现象:i)建立一个跨多个不同患者群体报告的同种免疫基本框架;ii)更全面地探讨支持关于血型抗原同种免疫的应答者/无应答者概念的文献报告;iii)总结已证明易导致个体发生同种免疫的机制,以确定这些因素如何将“应答者”与“无应答者”区分开来;iv)简要讨论一些预防可能易发生同种抗体产生的患者发生同种免疫的实用方法。