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基于李斯特菌的靶向 ISG15 疫苗在肾细胞癌中发挥抗肿瘤疗效

英文原题:A Listeria-based vaccine targeting ISG15 exerts anti-tumor efficacy in renal cell carcinoma.

查看英文原题

A Listeria-based vaccine targeting ISG15 exerts anti-tumor efficacy in renal cell carcinoma.

PubMed 2022/12/23(内容时间) Cancer Immunol Immunother Q1 · IF 5.8(JCR 2025)

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中文摘要

肾细胞癌(RCC)是泌尿系统癌症中致死率最高的形式,预计到2040年将成为美国男性中第四大常见肿瘤。除了目前预后较差、5年生存率几乎达不到15%之外,现有全身性疗法的耐药性普遍存在,也使得开发晚期RCC的新治疗方案成为迫切需求。干扰素刺激基因15(ISG15)是第一个被鉴定的类泛素修饰因子,因其在抗细胞内病原体天然免疫中的核心作用而受到深入研究。

然而,在本研究中,我们将ISG15鉴定为RCC中一种新型肿瘤相关抗原和预后标志物。此外,我们通过基于单核细胞增生李斯特菌(Lm)的疫苗Lm-LLO-ISG15,在皮下和原位RCC小鼠模型中针对升高的ISG15表达进行了治疗性靶向。Lm-LLO-ISG15治疗导致肿瘤浸润效应T细胞流入,并在皮下和原位RCC肿瘤模型中均产生显著的抗肿瘤疗效。Lm-LLO-ISG15治疗还产生了强烈的干扰素-γ反应,并吸引更多多功能T细胞进入肿瘤微环境。

重要的是,Lm-LLO-ISG15在RCC中的治疗疗效与抗PD-1和舒尼替尼——目前RCC患者的一线疗法——相当。总之,我们的工作表明,使用基于CTL的免疫疗法如Lm-LLO-ISG15靶向RCC中的ISG15,是一种有前景且可能可转化的治疗策略,以提高RCC患者的生存率。

展开英文摘要原文

Renal cell carcinoma (RCC) is the deadliest form of urological cancer and is projected to be the fourth most common neoplasm in the USA in males by 2040.

In addition to the current poor prognosis with 5-year survival rates hardly reaching 15%, the prevalence of resistance to currently available systemic therapies has also established an urgent need to develop new treatment regimen(s) for advanced RCC. Interferon-stimulated gene 15 (ISG15) is the first identified ubiquitin-like modifier and has been intensively studied for its central role in innate immunity against intracellular pathogens.

However, in this study, we identified ISG15 as a novel tumor-associated antigen and prognostic marker in RCC.

Further, we therapeutically targeted elevated ISG15 expression by means of a Listeria monocytogenes (Lm)-based vaccine, designated Lm-LLO-ISG15, in both subcutaneous and orthotopic RCC mouse models. Treatment with Lm-LLO-ISG15 resulted in an influx of tumor-infiltrating effector T cells and significant anti-tumor efficacy in both subcutaneous and orthotopic RCC tumor models. Treatment with Lm-LLO-ISG15 also generated a robust interferon-gamma response and attracted a larger pool of polyfunctional T cells into the tumor microenvironment.

Importantly, the therapeutic efficacy of Lm-LLO-ISG15 in RCC is comparable to that of anti-PD-1 and sunitinib, the current frontline therapies for RCC patients. Collectively, our work illustrates that targeting ISG15 in RCC with a CTL-based immunotherapy such as Lm-LLO-ISG15 is a promising and potentially translatable therapeutic strategy to enhance survival in RCC patients.

论文信息

作者
Nguyen HM、Oladejo M、Paulishak W、Wood LM
第一作者单位
Department of Immunotherapeutics and Biotechnology, Jerry H Hodge School of Pharmacy, Texas Tech University Health Sciences Center, Abilene, TX, USA.United States
通讯作者单位
Department of Immunotherapeutics and Biotechnology, Jerry H Hodge School of Pharmacy, Texas Tech University Health Sciences Center, Abilene, TX, USA. laurence.wood@ttuhsc.edu.United States
期刊
Cancer immunology, immunotherapy : CII2023 Sep
原文标识
PubMed 36562824 · DOI 10.1007/s00262-022-03352-9