Mahasongkram Kodchakorn, Glab-Ampai Kantaphon, Kaewchim Kanasap, Saenlom Thanatsaran, Chulanetra Monrat, Sookrung Nitat, Nathalang Oytip, Chaicumpa Wanpen
Center of Research Excellence in Therapeutic Proteins and Antibody Engineering, Department of Parasitology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.
Graduate Program in Immunology, Department of Immunology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.
Vaccines (Basel). 2023 Dec 7;11(12):1826. doi: 10.3390/vaccines11121826.
(1) Background: Understanding how advanced cancers evade host innate and adaptive immune opponents has led to cancer immunotherapy. Among several immunotherapeutic strategies, the reversal of immunosuppression mediated by regulatory T cells in the tumor microenvironment (TME) using blockers of immune-checkpoint signaling in effector T cells is the most successful treatment measure. Furthermore, agonists of T cell costimulatory molecules (CD40, 4-1BB, OX40) play an additional anti-cancer role to that of checkpoint blocking in combined therapy and serve also as adjuvant/neoadjuvant/induction therapy to conventional cancer treatments, such as tumor resection and radio- and chemo- therapies. (2) Methods and Results: In this study, novel agonistic antibodies to the OX40/CD134 ectodomain (EcOX40), i.e., fully human bivalent single-chain variable fragments (HuscFvs) linked to IgG Fc (bivalent HuscFv-Fcγ fusion antibodies) were generated by using phage-display technology and genetic engineering. The HuscFvs in the fusion antibodies bound to the cysteine-rich domain-2 of the EcOX40, which is known to be involved in OX40-OX40L signaling for NF-κB activation in T cells. The fusion antibodies caused proliferation, and increased the survival and cytokine production of CD3-CD28-activated human T cells. They showed enhancement trends for other effector T cell activities like granzyme B production and lysis of ovarian cancer cells when added to the activated T cells. (3) Conclusions: The novel OX40 agonistic fusion antibodies should be further tested step-by-step toward their safe use as an adjunctive non-immunogenic cancer immunotherapeutic agent.
(1)背景:了解晚期癌症如何逃避宿主的固有免疫和适应性免疫对手促使了癌症免疫疗法的发展。在多种免疫治疗策略中,使用效应T细胞中免疫检查点信号阻断剂来逆转肿瘤微环境(TME)中调节性T细胞介导的免疫抑制是最成功的治疗措施。此外,T细胞共刺激分子(CD40、4-1BB、OX40)的激动剂在联合治疗中除了具有检查点阻断作用外,还发挥额外的抗癌作用,并且还可作为传统癌症治疗(如肿瘤切除以及放疗和化疗)的辅助/新辅助/诱导治疗。(2)方法与结果:在本研究中,通过噬菌体展示技术和基因工程制备了针对OX40/CD134胞外域(EcOX40)的新型激动性抗体,即与IgG Fc连接的全人源二价单链可变片段(HuscFvs)(二价HuscFv-Fcγ融合抗体)。融合抗体中的HuscFvs与EcOX40富含半胱氨酸的结构域2结合,已知该结构域参与T细胞中NF-κB激活的OX40-OX40L信号传导。融合抗体可引起增殖,并提高CD3-CD28激活的人T细胞的存活率和细胞因子产生。当添加到活化的T细胞中时,它们对其他效应T细胞活性(如颗粒酶B产生和卵巢癌细胞裂解)显示出增强趋势。(3)结论:新型OX40激动性融合抗体应逐步进行进一步测试,以安全用作辅助性非免疫原性癌症免疫治疗药物。