Center for Immunity and Immunotherapies, Seattle Children's Research Institute , Seattle, WA , USA ; School of Medical Laboratory Science and Biotechnology, College of Medical Science and Technology, Taipei Medical University , Taipei , Taiwan.
Center for Immunity and Immunotherapies, Seattle Children's Research Institute , Seattle, WA , USA.
Front Immunol. 2014 Jan 6;4:502. doi: 10.3389/fimmu.2013.00502.
Neutralizing antibody formation against transgene products can represent a major complication following gene therapy with treatment of genetic diseases, such as hemophilia A. Although successful approaches have been developed to prevent the formation of anti-factor VIII (FVIII) antibodies, innovative strategies to overcome pre-existing anti-FVIII immune responses in FVIII-primed subjects are still lacking. Anti-FVIII neutralizing antibodies circulate for long periods in part due to persistence of memory B-cells. Anti-CD20 targets a variety of B-cells (pre-B-cells to mature/memory cells); therefore, we investigated the impact of B-cell depletion on anti-FVIII immune responses in hemophilia A mice using anti-CD20 combined with regulatory T (Treg) cell expansion using IL-2/IL-2mAb complexes plus rapamycin. We found that anti-CD20 alone can partially modulate anti-FVIII immune responses in both unprimed and FVIII-primed hemophilia A mice. Moreover, in mice treated with anti-CD20+IL-2/IL-2mAb complexes+rapamycin+FVIII, anti-FVIII antibody titers were significantly reduced in comparison to mice treated with regimens targeting only B or T cells. In addition, titers remained low after a second challenge with FVIII plasmid. Treg cells and activation markers were transiently and significantly increased in the groups treated with IL-2/IL-2mAb complexes; however, significant B-cell depletion was obtained in anti-CD20-treated groups. Importantly, both FVIII-specific antibody-secreting cells and memory B-cells were significantly reduced in mice treated with combination therapy. This study demonstrates that a combination regimen is highly promising as a treatment option for modulating anti-FVIII antibodies and facilitating induction of long-term tolerance to FVIII in hemophilia A mice.
针对转基因产物的中和抗体的形成可能是基因治疗遗传疾病(如血友病 A)的一个主要并发症。尽管已经开发出成功的方法来预防抗因子 VIII (FVIII) 抗体的形成,但在 FVIII 引发的受试者中克服预先存在的抗 FVIII 免疫反应的创新策略仍然缺乏。抗 FVIII 中和抗体在部分由于记忆 B 细胞的持续存在而在体内循环很长时间。抗 CD20 靶向多种 B 细胞(前 B 细胞至成熟/记忆细胞);因此,我们使用抗 CD20 结合使用 IL-2/IL-2mAb 复合物加雷帕霉素的调节性 T (Treg) 细胞扩增,研究了 B 细胞耗竭对血友病 A 小鼠抗 FVIII 免疫反应的影响。我们发现,抗 CD20 单独可以部分调节未引发和 FVIII 引发的血友病 A 小鼠的抗 FVIII 免疫反应。此外,在用抗 CD20+IL-2/IL-2mAb 复合物+雷帕霉素+FVIII 治疗的小鼠中,与仅用针对 B 或 T 细胞的方案治疗的小鼠相比,抗 FVIII 抗体滴度显著降低。此外,在用 FVIII 质粒再次挑战后,滴度仍保持较低水平。用 IL-2/IL-2mAb 复合物治疗的组中 Treg 细胞和激活标志物短暂且显著增加;然而,在抗 CD20 治疗组中获得了显著的 B 细胞耗竭。重要的是,用联合治疗治疗的小鼠中,FVIII 特异性抗体分泌细胞和记忆 B 细胞均显著减少。这项研究表明,联合治疗方案是一种很有前途的治疗选择,可用于调节抗 FVIII 抗体并促进血友病 A 小鼠对 FVIII 的长期耐受。