• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

镰状细胞病中红细胞同种免疫:2010 年的流行率。

Red blood cell alloimmunization in sickle cell disease: prevalence in 2010.

机构信息

State University of New York-Downstate Medical Center/Kings County Hospital Center, Brooklyn, NY 11203, USA.

出版信息

Transfusion. 2013 Apr;53(4):704-9. doi: 10.1111/j.1537-2995.2012.03796.x. Epub 2012 Jul 13.

DOI:10.1111/j.1537-2995.2012.03796.x
PMID:22804353
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5096391/
Abstract

BACKGROUND

Transfusion of red blood cells (RBCs) is frequently required for care of individuals with sickle cell disease (SCD). Alloimmunization rates are high and may be reduced by matching for RBC antigens that can cause alloimmunization.

STUDY DESIGN AND METHODS

During the PROACTIVE Feasibility Study, patients with SCD age 2 years or older admitted for pain without acute chest syndrome were enrolled for possible randomization to preventive blood transfusion or standard care. Transfusion and antibody histories were obtained at each site, and antibody screening was done, to assess transfusion burden and alloimmunization prevalence. Participating sites were surveyed regarding antigen matching practice.

RESULTS

A total of 237 patients (169 SS, 42 SC, 15 Sβ(0) -thalassemia, 11 Sβ(+) -thalassemia), 118 males and 119 females, were enrolled. Mean age was 19.3 years (range, 2.0-68.0); there were 122 children and 115 adults. A total of 75.8% had received at least a single transfusion of RBCs before the study. Thirty-four patients (14.4%) had a history of at least one alloantibody and 17 of these had more than one. When surveyed, 19 sites (83% of responders) reported antigen matching to at least include C, E, and K for transfusion of all patients with SCD.

CONCLUSION

Though antigen typing before transfusion of people with SCD and providing antigen-negative units is now widely employed by sickle cell centers, the alloimmunization rate remains quite high in contemporary sickle cell populations and may be due in large part to transfusions received at institutions not providing extended matching.

摘要

背景

镰状细胞病(SCD)患者常需要输注红细胞(RBC)进行治疗。同种免疫发生率较高,通过匹配可能引起同种免疫的 RBC 抗原可降低同种免疫发生率。

研究设计和方法

在 PROACTIVE 可行性研究中,年龄≥2 岁且因疼痛而无急性胸部综合征的 SCD 患者入院后,可能会被随机分配到预防性输血或标准治疗组。在每个地点获取输血和抗体史,并进行抗体筛查,以评估输血负担和同种免疫发生率。对参与的地点进行了关于抗原匹配实践的调查。

结果

共纳入 237 例患者(169 例 SS、42 例 SC、15 例 Sβ(0)-地中海贫血、11 例 Sβ(+) -地中海贫血,118 例男性和 119 例女性),平均年龄为 19.3 岁(范围 2.0-68.0);其中 122 例为儿童,115 例为成人。75.8%的患者在研究前至少接受过一次 RBC 输血。34 例(14.4%)有至少一次同种异体抗体史,其中 17 例有不止一种同种异体抗体史。调查时,19 个地点(83%的应答者)报告称,为所有 SCD 患者输血时,抗原匹配至少包括 C、E 和 K。

结论

虽然目前镰状细胞中心广泛采用在输血前对 SCD 患者进行抗原分型并提供抗原阴性单位,但在当代镰状细胞人群中同种免疫发生率仍然很高,这可能主要是由于在不提供扩展匹配的机构中接受的输血所致。

相似文献

1
Red blood cell alloimmunization in sickle cell disease: prevalence in 2010.镰状细胞病中红细胞同种免疫:2010 年的流行率。
Transfusion. 2013 Apr;53(4):704-9. doi: 10.1111/j.1537-2995.2012.03796.x. Epub 2012 Jul 13.
2
Alloimmunization in sickle cell anemia in the era of extended red cell typing.镰状细胞贫血症中延长红细胞定型检测时代的同种免疫反应
Pediatr Blood Cancer. 2013 Sep;60(9):1487-91. doi: 10.1002/pbc.24530. Epub 2013 Mar 18.
3
Red blood cell alloimmunization and minor red blood cell antigen phenotypes in transfused Ghanaian patients with sickle cell disease.红细胞同种免疫与输血的镰状细胞病加纳患者的小红细胞抗原表型。
Transfusion. 2019 Jun;59(6):2016-2022. doi: 10.1111/trf.15197. Epub 2019 Feb 13.
4
Red blood cell alloimmunization: lessons from sickle cell disease.红细胞同种免疫:镰状细胞病的经验教训
Transfusion. 2013 Apr;53(4):692-5. doi: 10.1111/trf.12146.
5
Red blood cell alloimmunization in sickle cell disease-prevalence and trends: a single-center cross-sectional study from United Kingdom.镰状细胞病中的红细胞同种免疫——患病率及趋势:一项来自英国的单中心横断面研究
Transfusion. 2013 Dec;53(12):3279-80. doi: 10.1111/trf.12382.
6
Predicting the effect of transfusing only phenotype-matched RBCs to patients with sickle cell disease: theoretical and practical implications.预测仅输注血型匹配红细胞对镰状细胞病患者的影响:理论与实际意义
Transfusion. 2002 Jun;42(6):684-90. doi: 10.1046/j.1537-2995.2002.00126.x.
7
Comparative study of alloimmunization against red cell antigens in sickle cell disease & thalassaemia major patients on regular red cell transfusion.镰状细胞病和重型地中海贫血患者定期红细胞输注后针对红细胞抗原同种免疫的对比研究。
Indian J Med Res. 2019 Jan;149(1):34-40. doi: 10.4103/ijmr.IJMR_940_17.
8
Delayed hemolytic transfusion reaction/hyperhemolysis syndrome in children with sickle cell disease.镰状细胞病患儿的迟发性溶血性输血反应/高溶血综合征
Pediatrics. 2003 Jun;111(6 Pt 1):e661-5. doi: 10.1542/peds.111.6.e661.
9
Economic evaluation of a hypothetical screening assay for alloimmunization risk among transfused patients with sickle cell disease.镰状细胞病输血患者同种免疫风险假设筛查试验的经济学评估。
Transfusion. 2014 Aug;54(8):2034-44. doi: 10.1111/trf.12585. Epub 2014 Feb 27.
10
Impact of Red Blood Cell Antigen Matching on Alloimmunization and Transfusion Complications in Patients with Sickle Cell Disease: A Systematic Review.红细胞抗原匹配对镰状细胞病患者同种免疫和输血并发症的影响:系统评价。
Transfus Med Rev. 2019 Jan;33(1):12-23. doi: 10.1016/j.tmrv.2018.07.003. Epub 2018 Jul 26.

引用本文的文献

1
Secretory Phospholipase A2 as a Promising Biomarker for Predicting Acute Chest Syndrome in Children With Sickle Cell Disease: A Systematic Review and Meta-Analysis.分泌型磷脂酶A2作为预测镰状细胞病患儿急性胸综合征的有前景生物标志物:一项系统评价和荟萃分析
Cureus. 2024 Sep 10;16(9):e69053. doi: 10.7759/cureus.69053. eCollection 2024 Sep.
2
Assessment of erythrocyte alloimmunization among patients treated at a Brazilian university hospital.巴西一家大学医院接受治疗的患者红细胞同种免疫评估。
Hematol Transfus Cell Ther. 2024 Nov;46 Suppl 5(Suppl 5):S128-S135. doi: 10.1016/j.htct.2024.04.128. Epub 2024 Sep 7.
3
and Genetic Polymorphisms Associated with Alloimmunisation in Sickle Cell Disease.与镰状细胞病同种免疫相关的遗传多态性。
Int J Mol Sci. 2023 Sep 2;24(17):13591. doi: 10.3390/ijms241713591.
4
Adverse events of red blood cell transfusions in patients with sickle cell disease.镰状细胞病患者输血的不良反应。
Transfus Apher Sci. 2022 Oct;61(5):103557. doi: 10.1016/j.transci.2022.103557. Epub 2022 Aug 29.
5
Medical and Non-medical Costs of Sickle Cell Disease and Treatments from a US Perspective: A Systematic Review and Landscape Analysis.从美国视角看镰状细胞病及其治疗的医疗和非医疗成本:系统评价与全景分析
Pharmacoecon Open. 2022 Jul;6(4):469-481. doi: 10.1007/s41669-022-00330-w. Epub 2022 Apr 26.
6
One third of alloantibodies in patients with sickle cell disease transfused with African blood are missed by the standard red blood cell test panel.镰状细胞病患者输注非洲血液后,标准红细胞检测 panel 会漏检三分之一的同种抗体。
Haematologica. 2021 Aug 1;106(8):2274-2276. doi: 10.3324/haematol.2021.278451.
7
Prevalence and risk factors for red blood cell alloimmunisation among sickle cell patients in Mwanza City, Tanzania.坦桑尼亚姆万扎市镰状细胞病患者红细胞同种免疫的患病率及危险因素
Afr J Lab Med. 2020 Sep 10;9(1):823. doi: 10.4102/ajlm.v9i1.823. eCollection 2020.
8
Development and validation of a universal blood donor genotyping platform: a multinational prospective study.开发和验证通用献血者基因分型平台:一项多国家前瞻性研究。
Blood Adv. 2020 Aug 11;4(15):3495-3506. doi: 10.1182/bloodadvances.2020001894.
9
The Allele and Anti-D Alloimmunization Present With High Frequency in Brazilian Sickle Cell Disease Patients.等位基因和抗-D同种免疫在巴西镰状细胞病患者中高频出现。
J Hematol. 2017 Oct;6(4):73-80. doi: 10.14740/jh316w. Epub 2017 Sep 20.
10
Blood transfusions for treating acute chest syndrome in people with sickle cell disease.输血治疗镰状细胞病患者的急性胸部综合征。
Cochrane Database Syst Rev. 2020 Jan 16;1(1):CD007843. doi: 10.1002/14651858.CD007843.pub4.

本文引用的文献

1
Red blood cell alloimmunization in sickle cell disease: pathophysiology, risk factors, and transfusion management.镰状细胞病中的红细胞同种免疫:病理生理学、危险因素及输血管理
Blood. 2012 Jul 19;120(3):528-37. doi: 10.1182/blood-2011-11-327361. Epub 2012 May 4.
2
Refining the value of secretory phospholipase A2 as a predictor of acute chest syndrome in sickle cell disease: results of a feasibility study (PROACTIVE).分泌型磷脂酶 A2 对镰状细胞病急性胸部综合征预测价值的改良:一项可行性研究(PROACTIVE)的结果。
Br J Haematol. 2012 Jun;157(5):627-36. doi: 10.1111/j.1365-2141.2012.09105.x. Epub 2012 Mar 30.
3
Molecular blood typing augments serologic testing and allows for enhanced matching of red blood cells for transfusion in patients with sickle cell disease.分子血液分型增强了血清学检测,并允许对镰状细胞病患者的红细胞进行更好的匹配,以进行输血。
Transfusion. 2012 Feb;52(2):381-8. doi: 10.1111/j.1537-2995.2011.03288.x. Epub 2011 Aug 9.
4
Extended red blood cell antigen matching for transfusions in sickle cell disease: a review of a 14-year experience from a single center (CME).红细胞延长抗原配血在镰状细胞病中的应用:单中心 14 年经验回顾(CME)。
Transfusion. 2011 Aug;51(8):1732-9. doi: 10.1111/j.1537-2995.2010.03045.x. Epub 2011 Feb 18.
5
How safe is blood, really?血液究竟有多安全?
Biologicals. 2010 Jan;38(1):100-4. doi: 10.1016/j.biologicals.2009.10.008. Epub 2010 Jan 15.
6
Molecular biology of the Rh system: clinical considerations for transfusion in sickle cell disease.Rh 系统的分子生物学:镰状细胞病输血的临床考虑因素。
Hematology Am Soc Hematol Educ Program. 2009:178-84. doi: 10.1182/asheducation-2009.1.178.
7
Transfusion management of patients with sickle cell disease: the continuing dilemma.镰状细胞病患者的输血管理:持续存在的困境
Transfusion. 2010 Jan;50(1):2-4. doi: 10.1111/j.1537-2995.2009.02527.x. Epub 2009 Nov 23.
8
Lack of Duffy antigen expression is associated with organ damage in patients with sickle cell disease.缺乏达菲抗原表达与镰状细胞病患者的器官损伤有关。
Transfusion. 2008 May;48(5):917-24. doi: 10.1111/j.1537-2995.2007.01622.x. Epub 2008 Feb 1.
9
The structure and function of the Rh antigen complex.Rh抗原复合体的结构与功能。
Semin Hematol. 2007 Jan;44(1):42-50. doi: 10.1053/j.seminhematol.2006.09.010.
10
Transfusion practices for patients with sickle cell disease at a major academic medical center.一家大型学术医疗中心镰状细胞病患者的输血治疗方法
Immunohematology. 2006;22(3):103-7.