Antigen density dictates RBC clearance, but not antigen modulation, following incompatible RBC transfusion in mice

被引:14
|
作者
Arthur, Connie M. [1 ]
Allen, Jerry William L. [1 ,2 ]
Verkerke, Hans [1 ]
Yoo, Justin [1 ]
Jajosky, Ryan P. [1 ]
Girard-Pierce, Kathryn [1 ]
Chonat, Satheesh [3 ]
Zerra, Patricia [1 ,3 ]
Maier, Cheryl [1 ]
Rha, Jen [1 ]
Fasano, Ross [1 ,3 ]
Josephson, Cassandra D. [1 ,3 ]
Roback, John D. [1 ]
Stowell, Sean R. [1 ,2 ]
机构
[1] Emory Univ, Sch Med, Dept Pathol & Lab Med, Ctr Transfus Med & Cellular Therapies, Atlanta, GA 30322 USA
[2] Harvard Med Sch, Brigham & Womens Hosp, Dept Pathol, Joint Program Transfus Med, Boston, MA 02115 USA
[3] Emory Univ, Sch Med, Dept Pediat, Aflac Canc & Blood Disorders Ctr, Atlanta, GA USA
基金
美国国家卫生研究院;
关键词
SICKLE-CELL-DISEASE; RED-BLOOD-CELLS; FC-GAMMA RECEPTORS; HYPERHEMOLYSIS SYNDROME; ADULT PATIENTS; MOUSE MODEL; ALLOIMMUNIZATION; COMPLEMENT; ANTIBODY; ALLOANTIBODIES;
D O I
10.1182/bloodadvances.2020002695
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Incompatible red blood cell (RBC) transfusion can result in life-threatening transfusion complications that can be challenging to manage in patients with transfusion-dependent anemia. However, not all incompatible RBC transfusions result in significant RBC removal. One factor that may regulate the outcome of incompatible RBC transfusion is the density of the incompatible antigen. Despite the potential influence of target antigen levels during incompatible RBC transfusion, a model system capable of defining the role of antigen density in this process has not been developed. In this study, we describe a novel model system of incompatible transfusion using donor mice that express different levels of the KEL antigen and recipients with varying anti-KEL antibody concentrations. Transfusion of KEL - RBCs that express high or moderate KEL antigen levels results in rapid antibody-mediated RBC clearance. In contrast, relatively little RBC clearance was observed following the transfusion of KEL+ RBCs that express low KEL antigen levels. Intriguingly, unlike RBC clearance, loss of the KEL antigen from the transfused RBCs occurred at a similar rate regardless of the KEL antigen density following an incompatible transfusion. In addition to antigen density, anti-KEL antibody levels also regulated RBC removal and KEL antigen loss, suggesting that antigen density and antibody levels dictate incompatible RBC transfusion outcomes. These results demonstrate that antibody-induced antigen loss and RBC clearance can occur at distinct antigen density thresholds, providing important insight into factors that may dictate the outcome of an incompatible RBC transfusion.
引用
收藏
页码:527 / 538
页数:12
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