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