Broka Derrick, Klein Shoshana, Shir Alexei, Schade Babette, Saxena Meera, Dasargyri Athanasia, Jarzebinska Anita, De Feyter Caroline, Bajic Davor, Colecchia David, D'Amico Lucia, Kitas Eric, Hikri Elad, Skowicki Michal Jerzy, Okoniewski Michal Jerzy, Baldino Laura, Qeriqi Besnik, Stanchina Elisa de, Schreiber Joerg, Buchi Melanie, Palivan Cornelia G, Benenson Yaakov, Zippelius Alfred, Fabbro Doriano, Scaltriti Maurizio, Mizrachi Aviram, Levitzki Alexander, Pombo-Villar Esteban, Zigler Maya
TargImmune Therapeutics, Basel 4057, Switzerland.
Department of Biological Chemistry, Silberman Life Sciences Institute, The Hebrew University of Jerusalem, Edmond J. Safra Campus, Jerusalem 9190401, Israel.
Proc Natl Acad Sci U S A. 2025 Jun 3;122(22):e2500489122. doi: 10.1073/pnas.2500489122. Epub 2025 May 29.
Aberrant activation and overexpression of the epidermal growth factor receptor (EGFR) occurs in various solid cancers and often correlates with poor outcome. The clinical benefit from EGFR-targeted therapies is usually short-lived, with resistance being driven by tumor heterogeneity and an immunosuppressive tumor microenvironment (TME). To address these limitations, we developed Targeted Apoptotic Immune Modulators (TAIM), a nonviral nanoparticle platform for the targeted delivery of polyinosine:polycytosine (polyIC), to simultaneously induce tumor cell death and activate antitumor immunity. The first TAIM compound, TAR001, was designed as a systemic treatment against metastatic EGFR-positive solid cancers. Here, we present TAR001's multifaceted mode of action. We demonstrate that TAR001 is selective toward EGFR-overexpressing cancers, provoking a pattern recognition response, apoptosis, cytokine secretion, and antitumor immunity. TAR001 modulates the TME, recruiting and activating both innate and adaptive immune cells. Systemic delivery of TAR001 markedly extends survival and inhibits tumor growth in multiple murine tumor models. TAR001 represents an innovative, safe, multimodal treatment approach with the potential to benefit patients with metastatic head and neck, non-small cell lung cancer, colorectal, renal, and triple-negative breast cancers. This unique modality utilizes a broad range of mechanisms to overcome the tumor's ability to escape apoptosis and immune cell activation.
表皮生长因子受体(EGFR)的异常激活和过表达发生在多种实体癌中,且常与不良预后相关。EGFR靶向治疗的临床益处通常是短暂的,肿瘤异质性和免疫抑制性肿瘤微环境(TME)会导致耐药性。为解决这些局限性,我们开发了靶向凋亡免疫调节剂(TAIM),这是一种用于靶向递送聚肌苷酸:聚胞嘧啶核苷酸(polyIC)的非病毒纳米颗粒平台,可同时诱导肿瘤细胞死亡并激活抗肿瘤免疫。首个TAIM化合物TAR001被设计用于针对转移性EGFR阳性实体癌的全身治疗。在此,我们展示TAR001的多方面作用模式。我们证明TAR001对EGFR过表达的癌症具有选择性,可引发模式识别反应、凋亡、细胞因子分泌和抗肿瘤免疫。TAR001调节TME,募集并激活先天免疫细胞和适应性免疫细胞。在多个小鼠肿瘤模型中,TAR001的全身递送显著延长了生存期并抑制了肿瘤生长。TAR001代表了一种创新、安全的多模式治疗方法,有可能使转移性头颈癌、非小细胞肺癌患者、结直肠癌、肾癌和三阴性乳腺癌患者受益。这种独特的模式利用多种机制来克服肿瘤逃避凋亡和免疫细胞激活的能力。