Wabnitz Hanna, Cruz-Leal Yoelys, Lazarus Alan H
Keenan Research Centre for Biomedical Science, St. Michael's Hospital, Unity Health Toronto, Toronto, Ontario, Canada.
Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
Transfusion. 2023 Mar;63(3):619-628. doi: 10.1111/trf.17232. Epub 2023 Jan 2.
Despite the vast antigen disparity between donor and recipient red blood cells (RBCs), only 2%-6% of transfusion patients mount an alloantibody response. Recently, RBC antigen density has been proposed as one of the factors that can influence alloimmunization, however, there has been no characterization of the role of antigen density along with RBC dose in primary and secondary immunization.
To generate RBCs that express distinct antigen copy numbers, different quantities of hen egg lysozyme (HEL) were coupled to murine RBCs. The HEL-RBCs were subsequently transfused into recipient mice at different RBC doses and their HEL-specific IgM, IgG, and IgG subclass response was evaluated.
Productive immune responses could be generated through a high copy number antigen transfused at low RBC doses or a low copy number transfused at high RBC doses. Further, primary but submaximal humoral immunization predominantly induced the IgG2b and IgG3 subclasses. In contrast, a maximal primary immunization or a secondary immunization induced all four IgG subclasses.
Our results confirm the existence of an antigen threshold for productive immune responses but indicate that a high antigen copy number alone might not be enough to induce a response, but rather a combination of both antigen copy number and cell dosage may determine the outcome of immunization. Further, this study provides a proof of concept that the IgG subclass composition can be an indicator of the level of RBC alloimmunization as well as discern between primary and secondary immunization at least in this murine model.
尽管供体和受体红细胞(RBC)之间存在巨大的抗原差异,但只有2%-6%的输血患者会产生同种抗体反应。最近,红细胞抗原密度被认为是影响同种免疫的因素之一,然而,尚未有关于抗原密度与红细胞剂量在初次和二次免疫中作用的特征描述。
为了生成表达不同抗原拷贝数的红细胞,将不同量的鸡蛋清溶菌酶(HEL)与小鼠红细胞偶联。随后将HEL-红细胞以不同的红细胞剂量输注到受体小鼠体内,并评估其针对HEL的IgM、IgG和IgG亚类反应。
通过低红细胞剂量输注的高拷贝数抗原或高红细胞剂量输注的低拷贝数抗原均可产生有效的免疫反应。此外,初次但次最大体液免疫主要诱导IgG2b和IgG3亚类。相比之下,最大初次免疫或二次免疫可诱导所有四种IgG亚类。
我们的结果证实了有效免疫反应存在抗原阈值,但表明仅高抗原拷贝数可能不足以诱导反应,而是抗原拷贝数和细胞剂量的组合可能决定免疫结果。此外,本研究提供了一个概念证明,即IgG亚类组成可以作为红细胞同种免疫水平的指标,并且至少在这个小鼠模型中可以区分初次免疫和二次免疫。