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本文引用的文献

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Immunological complications of blood transfusions.输血的免疫并发症
Presse Med. 2016 Jul-Aug;45(7-8 Pt 2):e313-24. doi: 10.1016/j.lpm.2016.06.024. Epub 2016 Aug 4.
2
Red-blood-cell alloimmunisation in relation to antigens' exposure and their immunogenicity: a cohort study.红细胞同种免疫与抗原暴露及其免疫原性的关系:一项队列研究。
Lancet Haematol. 2016 Jun;3(6):e284-92. doi: 10.1016/S2352-3026(16)30019-9. Epub 2016 May 9.
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CD8+ T cells mediate antibody-independent platelet clearance in mice.CD8 + T细胞介导小鼠体内不依赖抗体的血小板清除。
Blood. 2016 Apr 7;127(14):1823-7. doi: 10.1182/blood-2015-10-673426. Epub 2016 Jan 19.
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Impact of red blood cell alloimmunization on sickle cell disease mortality: a case series.红细胞同种免疫对镰状细胞病死亡率的影响:病例系列研究
Transfusion. 2016 Jan;56(1):107-14. doi: 10.1111/trf.13379. Epub 2015 Oct 28.
5
Review on immunosuppression in liver transplantation.肝移植中的免疫抑制综述。
World J Hepatol. 2015 Jun 8;7(10):1355-68. doi: 10.4254/wjh.v7.i10.1355.
6
Age of transfused blood in critically ill adults.危重症成人输注血液的年龄。
N Engl J Med. 2015 Apr 9;372(15):1410-8. doi: 10.1056/NEJMoa1500704. Epub 2015 Mar 17.
7
Factors Influencing RBC Alloimmunization: Lessons Learned from Murine Models.影响 RBC 同种免疫的因素:从鼠模型中获得的经验教训。
Transfus Med Hemother. 2014 Nov;41(6):406-19. doi: 10.1159/000368995. Epub 2014 Nov 17.
8
B10 cells: a functionally defined regulatory B cell subset.B10细胞:一种功能上定义的调节性B细胞亚群。
J Immunol. 2015 Feb 15;194(4):1395-401. doi: 10.4049/jimmunol.1401329.
9
RhD Specific Antibodies Are Not Detectable in HLA-DRB1(*)1501 Mice Challenged with Human RhD Positive Erythrocytes.在用人RhD阳性红细胞攻击的HLA - DRB1(*)1501小鼠中未检测到RhD特异性抗体。
Adv Hematol. 2014;2014:470242. doi: 10.1155/2014/470242. Epub 2014 Dec 31.
10
Red blood cell alloimmunization is influenced by recipient inflammatory state at time of transfusion in patients with sickle cell disease.红细胞同种免疫受镰状细胞病患者输血时受体炎症状态的影响。
Br J Haematol. 2015 Jan;168(2):291-300. doi: 10.1111/bjh.13123. Epub 2014 Sep 26.

抗原密度决定红细胞输血后的免疫反应性。

Antigen Density Dictates Immune Responsiveness following Red Blood Cell Transfusion.

作者信息

Arthur Connie M, Patel Seema R, Smith Nicole H, Bennett Ashley, Kamili Nourine A, Mener Amanda, Gerner-Smidt Christian, Sullivan Harold C, Hale J Scott, Wieland Andreas, Youngblood Benjamin, Zimring James C, Hendrickson Jeanne E, Stowell Sean R

机构信息

Center for Transfusion Medicine and Cellular Therapies, Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA 30322.

Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322.

出版信息

J Immunol. 2017 Apr 1;198(7):2671-2680. doi: 10.4049/jimmunol.1601736. Epub 2017 Mar 1.

DOI:10.4049/jimmunol.1601736
PMID:28250159
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5777137/
Abstract

Although RBC transfusion can result in the development of anti-RBC alloantibodies that increase the probability of life-threatening hemolytic transfusion reactions, not all patients generate anti-RBC alloantibodies. However, the factors that regulate immune responsiveness to RBC transfusion remain incompletely understood. One variable that may influence alloantibody formation is RBC alloantigen density. RBC alloantigens exist at different densities on the RBC surface and likewise exhibit distinct propensities to induce RBC alloantibody formation. However, although distinct alloantigens reside on the RBC surface at different levels, most alloantigens also represent completely different structures, making it difficult to separate the potential impact of differences in Ag density from other alloantigen features that may also influence RBC alloimmunization. To address this, we generated RBCs that stably express the same Ag at different levels. Although exposure to RBCs with higher Ag levels induces a robust Ab response, RBCs bearing low Ag levels fail to induce RBC alloantibodies. However, exposure to low Ag-density RBCs is not without consequence, because recipients subsequently develop Ag-specific tolerance. Low Ag-density RBC-induced tolerance protects higher Ag-density RBCs from immune-mediated clearance, is Ag specific, and occurs through the induction of B cell unresponsiveness. These results demonstrate that Ag density can potently impact immune outcomes following RBC transfusion and suggest that RBCs with altered Ag levels may provide a unique tool to induce Ag-specific tolerance.

摘要

尽管红细胞输血可导致抗红细胞同种抗体的产生,从而增加危及生命的溶血性输血反应的可能性,但并非所有患者都会产生抗红细胞同种抗体。然而,调节对红细胞输血免疫反应性的因素仍未完全了解。一个可能影响同种抗体形成的变量是红细胞同种抗原密度。红细胞同种抗原以不同密度存在于红细胞表面,同样表现出诱导红细胞同种抗体形成的不同倾向。然而,尽管不同的同种抗原以不同水平存在于红细胞表面,但大多数同种抗原也代表完全不同的结构,因此难以将抗原密度差异的潜在影响与可能也影响红细胞同种免疫的其他同种抗原特征区分开来。为了解决这个问题,我们生成了在不同水平稳定表达相同抗原的红细胞。尽管暴露于具有较高抗原水平的红细胞会诱导强烈的抗体反应,但携带低抗原水平的红细胞未能诱导红细胞同种抗体。然而,暴露于低抗原密度的红细胞并非没有后果,因为受者随后会产生抗原特异性耐受。低抗原密度红细胞诱导的耐受可保护较高抗原密度的红细胞免受免疫介导的清除,具有抗原特异性,并且通过诱导B细胞无反应性而发生。这些结果表明,抗原密度可有力地影响红细胞输血后的免疫结果,并表明抗原水平改变的红细胞可能提供一种诱导抗原特异性耐受的独特工具。