Center for Cancer and Immunology Research, Children's Research Institute, Children's National Health System, Washington, DC, 20010, USA.
OncoImmune, Inc., Rockville, MD, 20852, USA.
Cell Res. 2018 Apr;28(4):433-447. doi: 10.1038/s41422-018-0012-z. Epub 2018 Feb 20.
Anti-CTLA-4 monoclonal antibodies (mAbs) confer a cancer immunotherapeutic effect (CITE) but cause severe immunotherapy-related adverse events (irAE). Targeting CTLA-4 has shown remarkable long-term benefit and thus remains a valuable tool for cancer immunotherapy if the irAE can be brought under control. An animal model, which recapitulates clinical irAE and CITE, would be valuable for developing safer CTLA-4-targeting reagents. Here, we report such a model using mice harboring the humanized Ctla4 gene. In this model, the clinically used drug, Ipilimumab, induced severe irAE especially when combined with an anti-PD-1 antibody; whereas another mAb, L3D10, induced comparable CITE with very mild irAE under the same conditions. The irAE corresponded to systemic T cell activation and resulted in reduced ratios of regulatory to effector T cells (Treg/Teff) among autoreactive T cells. Using mice that were either homozygous or heterozygous for the human allele, we found that the irAE required bi-allelic engagement, while CITE only required monoallelic engagement. As with the immunological distinction for monoallelic vs bi-allelic engagement, we found that bi-allelic engagement of the Ctla4 gene was necessary for preventing conversion of autoreactive T cells into Treg cells. Humanization of L3D10, which led to loss of blocking activity, further increased safety without affecting the therapeutic effect. Taken together, our data demonstrate that complete CTLA-4 occupation, systemic T cell activation and preferential expansion of self-reactive T cells are dispensable for tumor rejection but correlate with irAE, while blocking B7-CTLA-4 interaction impacts neither safety nor efficacy of anti-CTLA-4 antibodies. These data provide important insights for the clinical development of safer and potentially more effective CTLA-4-targeting immunotherapy.
抗 CTLA-4 单克隆抗体(mAbs)赋予癌症免疫治疗效果(CITE),但会引起严重的免疫治疗相关不良反应(irAE)。靶向 CTLA-4 已显示出显著的长期获益,因此,如果能控制 irAE,它仍然是癌症免疫治疗的有价值工具。能够重现临床 irAE 和 CITE 的动物模型对于开发更安全的 CTLA-4 靶向试剂将非常有价值。在这里,我们报告了一种使用携带人源化 Ctla4 基因的小鼠的此类模型。在该模型中,临床使用的药物伊匹单抗(Ipilimumab)在与抗 PD-1 抗体联合使用时会引起严重的 irAE;而另一种 mAb L3D10 在相同条件下引起相似的 CITE,仅有非常轻微的 irAE。irAE 对应于全身 T 细胞激活,并导致自身反应性 T 细胞中调节性 T 细胞(Treg/Teff)的比例降低。使用纯合或杂合携带人等位基因的小鼠,我们发现 irAE 需要双等位基因结合,而 CITE 仅需要单等位基因结合。与单等位基因和双等位基因结合的免疫学区别一样,我们发现 Ctla4 基因的双等位基因结合对于防止自身反应性 T 细胞转化为 Treg 细胞是必需的。L3D10 的人源化导致阻断活性丧失,进一步提高了安全性而不影响治疗效果。总的来说,我们的数据表明,完全 CTLA-4 占据、全身 T 细胞激活和自身反应性 T 细胞的优先扩增对于肿瘤排斥是不必要的,但与 irAE 相关,而阻断 B7-CTLA-4 相互作用既不影响抗 CTLA-4 抗体的安全性也不影响其疗效。这些数据为开发更安全和潜在更有效的 CTLA-4 靶向免疫疗法提供了重要的见解。