Department of Gastroenterological and Transplant Surgery, Applied Life Sciences, Institute of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
PLoS One. 2018 Oct 15;13(10):e0204880. doi: 10.1371/journal.pone.0204880. eCollection 2018.
Although many anticancer agents for gastric cancer have been developed, the prognosis for many patients remains poor. Recently, costimulatory immune molecules that reactivate antitumor immune responses by utilizing the host immune system have attracted attention as new therapeutic strategies. CD137 is a costimulatory molecule that reportedly potentiates the antitumor activity of tumor-targeting monoclonal antibodies (mAbs) by enhancing antibody-dependent cellular cytotoxicity. However, it remains unclear whether CD137 stimulates tumor-regulatory activity in gastric cancer. In this study, we investigated the antitumor effects of CD137 stimulation on gastric cancer cells administered tumor-targeting mAbs. Our results showed that human natural killer (NK) cells were activated by expressing CD137 after encountering trastuzumab-coated gastric cancer cells, and that stimulation of activated NK cells in the presence of trastuzumab and recombinant human CD137 ligand (rhCD137L) enhanced cytotoxicity and release of cytokines (IFN-γ, TNF, granzyme A, or granzyme B) as compared with activated NK cells with trastuzumab alone (p < 0.05). By combination treatment with rhCD137L, similar effects were obtained regarding cancer cell cytotoxicity in the presence of cetuximab (p < 0.01). Moreover, we revealed that CD137 expression was dependent upon the affinity between the Fc portion of the antibodies and FcγRIIIa of NK cells based on results indicating that human IgG1 and IgG3 subclasses enhanced CD137 expression (p < 0.001). These results confirmed that FcγRIIIA polymorphisms (158 V/V) enhanced CD137 expression to a greater degree than 158 F polymorphisms (p = 0.014). Our results suggested that CD137 stimulation could promote the effects of tumor-targeting mAbs in gastric cancer, and that further investigation of antibody binding affinity and in vivo activities might improve therapeutic strategies related to the treatment of gastric cancer patients.
尽管已经开发出许多用于胃癌的抗癌药物,但许多患者的预后仍然不佳。最近,利用宿主免疫系统重新激活抗肿瘤免疫反应的共刺激免疫分子作为新的治疗策略引起了关注。CD137 是一种共刺激分子,据报道通过增强抗体依赖性细胞毒性增强肿瘤靶向单克隆抗体(mAb)的抗肿瘤活性。然而,CD137 是否刺激胃癌中的肿瘤调节活性仍不清楚。在这项研究中,我们研究了 CD137 刺激对给予肿瘤靶向 mAb 的胃癌细胞的抗肿瘤作用。我们的结果表明,当遇到曲妥珠单抗包被的胃癌细胞时,人自然杀伤(NK)细胞通过表达 CD137 而被激活,并且在曲妥珠单抗和重组人 CD137 配体(rhCD137L)存在下刺激激活的 NK 细胞增强了细胞毒性和细胞因子(IFN-γ、TNF、颗粒酶 A 或颗粒酶 B)的释放,与单独用曲妥珠单抗激活的 NK 细胞相比(p < 0.05)。通过与 rhCD137L 联合治疗,在使用西妥昔单抗的情况下也获得了类似的癌细胞杀伤作用(p < 0.01)。此外,我们揭示 CD137 表达依赖于抗体的 Fc 部分与 NK 细胞的 FcγRIIIa 之间的亲和力,结果表明人 IgG1 和 IgG3 亚类增强了 CD137 表达(p < 0.001)。这些结果证实,FcγRIIIA 多态性(158 V/V)比 158 F 多态性更能增强 CD137 表达(p = 0.014)。我们的结果表明,CD137 刺激可以增强胃癌中肿瘤靶向 mAb 的作用,并且进一步研究抗体结合亲和力和体内活性可能会改善与治疗胃癌患者相关的治疗策略。