York Elizabeth S, Dratch Benjamin D, Ito Jasmine, Horwitz Samantha M, Emamian Sahand, Ambarian Joseph A, Gill Surinder, Jones Jayre, Chonat Satheesh, Lollar Pete, Meeks Shannon L, Davis Katherine M, Batsuli Glaivy
Department of Pediatrics, Stanford University, Palo Alto, California, USA; Department of Pediatrics, Emory University, Atlanta, Georgia, USA; Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, Georgia, USA.
Department of Chemistry, Emory University, Atlanta, Georgia, USA.
J Thromb Haemost. 2025 Feb;23(2):440-457. doi: 10.1016/j.jtha.2024.10.017. Epub 2024 Oct 28.
The most significant treatment complication for patients with hemophilia A is the development of neutralizing immunoglobins (Igs) G, termed inhibitors, against factor VIII (FVIII), which prevent FVIII replacement therapy. Low titers of FVIII-specific IgMs have been identified in hemophilia A patients with and without inhibitors, as well as in healthy individuals. However, the duration and influence of IgMs on the immune response to FVIII remains unclear.
To characterize the binding interactions of persistently secreted FVIII-specific IgMs in hemophilia A mice and assess their effect on IgG antibody development.
Splenic-derived monoclonal antibodies (mAbs) from immunized FVIII knockout mice were isolated and purified using hybridoma technology. Binding interactions were assessed utilizing a novel fluid-phase enzyme-linked immunosorbent assay and computational modeling with High Ambiguity-Driven protein-protein DOCKing to account for weak IgM binding.
Sixteen porcine cross-reactive and noninhibitory FVIII-specific IgM mAbs were identified. RNA sequencing of FVIII-specific IgMs revealed 13 unique variable, diversity, and joining (VDJ)/variable and joining (VJ) sequences indicating derivation from 13 unique B cell clones. The IgMs demonstrated polyclonal and polyreactive binding to FVIII in vitro and in silico. Molecular docking studies with reconstructed IgM variable, diversity, and joining/variable and joining regions identified frequent IgM interactions with amino acid residues K376, T381, K437, R2215, or K2249 within the FVIII A2 and C2 domains. Injections of individual IgMs prior to FVIII exposure and co-injection of FVIII/IgM immune complexes did not affect de novo FVIII antibody production.
Persistent FVIII-specific IgMs are polyclonal but preferentially bind the A2 and C2 domains. FVIII/IgM immune complex formation does not significantly alter inhibitor development.
甲型血友病患者最严重的治疗并发症是产生针对凝血因子VIII(FVIII)的中和免疫球蛋白G(称为抑制剂),这会阻碍FVIII替代疗法。在有或没有抑制剂的甲型血友病患者以及健康个体中均已鉴定出低滴度的FVIII特异性IgM。然而,IgM对FVIII免疫反应的持续时间和影响仍不清楚。
表征甲型血友病小鼠中持续分泌的FVIII特异性IgM的结合相互作用,并评估其对IgG抗体产生的影响。
使用杂交瘤技术从免疫的FVIII基因敲除小鼠中分离并纯化脾源单克隆抗体(mAb)。利用新型液相酶联免疫吸附测定法和高模糊度驱动的蛋白质-蛋白质对接计算模型评估结合相互作用,以考虑弱IgM结合。
鉴定出16种猪交叉反应性和非抑制性FVIII特异性IgM单克隆抗体。FVIII特异性IgM的RNA测序揭示了13个独特的可变、多样和连接(VDJ)/可变和连接(VJ)序列,表明它们源自13个独特的B细胞克隆。这些IgM在体外和计算机模拟中均显示出对FVIII的多克隆和多反应性结合。对重构的IgM可变、多样和连接/可变和连接区域进行的分子对接研究确定,IgM与FVIII A2和C2结构域内的氨基酸残基K376、T381、K437、R2215或K2249频繁相互作用。在暴露于FVIII之前注射单个IgM以及共同注射FVIII/IgM免疫复合物均不影响FVIII抗体的从头产生。
持续存在的FVIII特异性IgM是多克隆的,但优先结合A2和C2结构域。FVIII/IgM免疫复合物的形成不会显著改变抑制剂的产生。