Li Shulin
The University of Texas MD Anderson Cancer Center.
Res Sq. 2024 Oct 29:rs.3.rs-5104493. doi: 10.21203/rs.3.rs-5104493/v1.
Tumor-targeted T-cell therapies of various types have been booming, but T-cell therapy is limited by its inability to penetrate the collagen barrier surrounding tumors. The destruction of tumor collagen is significant because collagen both suppresses T cells and contributes to the formation of the extracellular matrix. Our previously reported cell surface vimentin (CSV)-targeted and membrane-anchored IL12-armed (attIL12) T cells can reduce collagen production by killing cancer-associated fibroblasts, thereby increasing T-cell infiltration. However, attIL12-T cells cannot reduce collagen expression by tumors that highly express CCKAR. In this study, we discovered that CCKAR directly boosts collagen production by tumor cells in vitro and in vivo. attIL12-modified tumor-infiltrating lymphocytes (TILs) disabled collagen production by CCKAR-high autologous tumor cells in vitro and sarcoma patient-derived xenografts (PDXs) in vivo. This disruption of collagen production by tumor cells required a simultaneous interaction between the CSV on autologous tumor cells, which is targeted by attIL12, and HLA-TCR on attIL12-TILs; when either interaction was abrogated, collagen production and CCKAR expression were not shut down. Mechanistically, the interaction between attIL12-TILs and autologous tumor cells synergized IFNγ production, which in combination with CCKAR downregulation reduced collagen expression through suppression of both TGFβ-stimulated SMAD activation and CCKAR-AKT signaling. Diminishing collagen expression from tumor cells significantly increased T-cell infiltration and improved tumor growth inhibition in PDX sarcomas. This study thus uncovers the first tumor collagen-disrupting T-cell therapy we know of. This is significant because collagen is enriched in most high-grade CCKAR+ human sarcomas. Thus, this attIL12-TIL therapy holds great clinical potential for boosting T-cell infiltration in high-grade, collagen-rich tumors.
各种类型的肿瘤靶向性T细胞疗法蓬勃发展,但T细胞疗法受到其无法穿透肿瘤周围胶原屏障的限制。肿瘤胶原的破坏意义重大,因为胶原既能抑制T细胞,又有助于细胞外基质的形成。我们之前报道的细胞表面波形蛋白(CSV)靶向且膜锚定白细胞介素12武装(attIL12)的T细胞可通过杀死癌症相关成纤维细胞来减少胶原生成,从而增加T细胞浸润。然而,attIL12-T细胞无法降低高表达CCKAR的肿瘤的胶原表达。在本研究中,我们发现CCKAR在体外和体内均可直接促进肿瘤细胞的胶原生成。attIL12修饰的肿瘤浸润淋巴细胞(TILs)在体外可使高表达CCKAR的自体肿瘤细胞以及在体内使肉瘤患者来源的异种移植瘤(PDXs)的胶原生成失活。肿瘤细胞胶原生成的这种破坏需要attIL12靶向的自体肿瘤细胞上的CSV与attIL12-TILs上的HLA-TCR之间同时相互作用;当任何一种相互作用被消除时,胶原生成和CCKAR表达都不会被关闭。从机制上讲,attIL12-TILs与自体肿瘤细胞之间的相互作用协同促进了IFNγ的产生,IFNγ与CCKAR下调相结合,通过抑制TGFβ刺激的SMAD激活和CCKAR-AKT信号传导来降低胶原表达。减少肿瘤细胞的胶原表达可显著增加T细胞浸润,并改善PDX肉瘤中的肿瘤生长抑制。因此,本研究揭示了我们所知的第一种破坏肿瘤胶原的T细胞疗法。这具有重要意义,因为胶原在大多数高级别CCKAR+人类肉瘤中含量丰富。因此,这种attIL12-TIL疗法在促进高级别、富含胶原的肿瘤中的T细胞浸润方面具有巨大的临床潜力。