Steele Hope, Willicut Ashley, Dell Garrison, Ghastine Andrew, Nguyen Xinh-Xinh, Lembicz Paul, Doerflein Hailey, Suchoski Therese, Kato Elizabeth, Feghali-Bostwick Carol, Croft Michael, Herro Rana
Division of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Immunology Graduate Program, University of Cincinnati, Cincinnati, OH, United States.
J Immunol. 2025 Apr 1;214(4):808-817. doi: 10.1093/jimmun/vkaf002.
Currently, anti-inflammatory drugs fail to reduce pulmonary fibrosis and tissue remodeling in the clinic. Thus, there is an unmet need to develop novel antifibrotic drugs capable of reversing disease. Our lab has identified two novel mediators of pulmonary fibrosis belonging to the tumor necrosis factor superfamily (TNFSF), LIGHT (TNFSF14) and TL1A (TNFSF15). Aside from their inflammatory roles, LIGHT and TL1A can directly activate structural cells involved in fibrosis, which express their receptors. Here, we show that LIGHT and TL1A receptors are both significantly elevated in patient pulmonary fibrosis biopsies as compared with healthy control lungs. Using gain-of-function studies, we found that LIGHT and TL1A can drive airway remodeling independently of one another. Furthermore, these TNFSF members synergize to maximize airway inflammation and fibrosis. We show that the combinatorial blockade of LIGHT and TL1A limits transforming growth factor β-driven profibrotic effects on fibroblasts in vitro. Moreover, LIGHT and TL1A stimulation of human epithelial cells and fibroblasts reveal distinct fibrotic signatures, including additive and synergistic profibrotic activities, in addition to some redundant profibrotic functions. Importantly, using antagonistic reagents neutralizing both LIGHT and TL1A signaling concomitantly post-disease onset in a bleomycin mouse model of pulmonary fibrosis, we observe a significant decrease in collagen deposition and smooth muscle accumulation as opposed to respective monotherapies blocking each molecule in isolation. This work highlights a therapeutic need to concomitantly target LIGHT and TL1A for treatment of pulmonary fibrosis disorders in humans.
目前,抗炎药物在临床上未能减轻肺纤维化和组织重塑。因此,开发能够逆转疾病的新型抗纤维化药物存在未满足的需求。我们实验室已经鉴定出两种属于肿瘤坏死因子超家族(TNFSF)的新型肺纤维化介质,即LIGHT(TNFSF14)和TL1A(TNFSF15)。除了其炎症作用外,LIGHT和TL1A还可直接激活参与纤维化的结构细胞,这些细胞表达它们的受体。在这里,我们表明与健康对照肺相比,患者肺纤维化活检组织中LIGHT和TL1A受体均显著升高。通过功能获得性研究,我们发现LIGHT和TL1A可彼此独立地驱动气道重塑。此外,这些TNFSF成员协同作用以最大化气道炎症和纤维化。我们表明,联合阻断LIGHT和TL1A可限制体外转化生长因子β对成纤维细胞的促纤维化作用。此外,LIGHT和TL1A对人上皮细胞和成纤维细胞的刺激揭示了不同的纤维化特征,包括相加和协同的促纤维化活性,以及一些冗余的促纤维化功能。重要的是,在博来霉素诱导的肺纤维化小鼠模型中,在疾病发作后使用拮抗试剂同时中和LIGHT和TL1A信号,我们观察到与单独阻断每个分子的单一疗法相比,胶原沉积和平滑肌积聚显著减少。这项工作强调了同时靶向LIGHT和TL1A治疗人类肺纤维化疾病的治疗需求。