Tessa Therapeutics Ltd, Singapore 138673, Singapore.
Center for Cell and Gene Therapy, Texas Children's Hospital, Houston Methodist Hospital, and Baylor College of Medicine, Houston, TX 77030, USA; Department of Pathology and Immunology, Baylor College of Medicine, Houston, TX 77030, USA; Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA; Texas Children's Cancer and Hematology Centers, Baylor College of Medicine, Houston, TX 77030, USA; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX 77030, USA.
Mol Ther. 2024 Oct 2;32(10):3504-3521. doi: 10.1016/j.ymthe.2024.06.037. Epub 2024 Jun 29.
The chimeric antigen receptor (CAR) derived from the CD30 specific murine antibody, HRS-3, has produced promising clinical efficacy with a favorable safety profile in the treatment of relapsed or refractory CD30-positive lymphomas. However, persistence of the autologous CAR-T cells was brief, and many patients relapsed a year after treatment. The lack of persistence may be attributed to the use of a wild-type immunoglobulin (Ig)G1 spacer that can associate with Fc receptors. We first identified the cysteine-rich domain (CRD) 5 of CD30 as the primary binding epitope of HRS-3 and armed with this insight, attempted to improve the HRS-3 CAR functionality with a panel of novel spacer designs. We demonstrate that HRS-3 CARs with OX40 and 4-1BB derived spacers exhibited similar anti-tumor efficacy, circumvented interactions with Fc receptors, and secreted lower levels of cytokines in vitro than a CAR employing the IgG1 spacer. Humanization of the HRS-3 scFv coupled with the 4-1BB spacer preserved potent on-target, on-tumor efficacy, and on-target, off-tumor safety. In a lymphoma mouse model of high tumor burden, T cells expressing humanized HRS-3 CD30.CARs with the 4-1BB spacer potently killed tumors with low levels of circulating inflammatory cytokines, providing a promising candidate for future clinical development in the treatment of CD30-positive malignancies.
嵌合抗原受体(CAR)来源于 CD30 特异性鼠抗体 HRS-3,在治疗复发或难治性 CD30 阳性淋巴瘤方面具有良好的安全性和有前景的临床疗效。然而,自体 CAR-T 细胞的持久性短暂,许多患者在治疗一年后复发。持久性差可能归因于使用可以与 Fc 受体结合的野生型免疫球蛋白(Ig)G1 间隔子。我们首先确定 CD30 的富含半胱氨酸结构域(CRD)5 是 HRS-3 的主要结合表位,并利用这一见解,尝试用一系列新型间隔子设计来改进 HRS-3 CAR 的功能。我们证明,带有 OX40 和 4-1BB 衍生间隔子的 HRS-3 CAR 具有相似的抗肿瘤功效,规避了与 Fc 受体的相互作用,并在体外分泌的细胞因子水平低于使用 IgG1 间隔子的 CAR。HRS-3 scFv 的人源化与 4-1BB 间隔子相结合,保留了强大的靶标、肿瘤内疗效和靶标、肿瘤外安全性。在高肿瘤负荷的淋巴瘤小鼠模型中,表达人源化 HRS-3 CD30.CAR 与 4-1BB 间隔子的 T 细胞能够强力杀伤肿瘤,同时循环中炎症细胞因子水平较低,为未来治疗 CD30 阳性恶性肿瘤的临床开发提供了有前景的候选药物。