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鼻内给予分泌 IL-15/IL-15Rα的重组新孢子虫可抑制肺转移性黑色素瘤的发展

英文原题:Nasal administration of recombinant Neospora caninum secreting IL-15/IL-15Rα inhibits metastatic melanoma development in lung.

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Nasal administration of recombinant Neospora caninum secreting IL-15/IL-15Rα inhibits metastatic melanoma development in lung.

PubMed 2023/05/01(内容时间) J Immunother Cancer Q1 · IF 11.7(JCR 2025)

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研究概要

通过鼻内给药这一无创途径给予分泌 IL-15/IL-15Rα的 N.

研究思路结论见上方概要

转移是许多癌症类型导致死亡的主要原因,而肺与肝、脑和骨一样,是最常见的转移部位之一。在黑色素瘤中,85%的晚期患者存在肺转移。局部给药可以增强对转移灶的靶向性,同时限制全身细胞毒性。因此,鼻内给予免疫治疗药物似乎是优先靶向肺转移并降低其在癌症死亡率中负担的一种有前景的方法。基于某些微生物可诱导肿瘤微环境的急性感染,从而导致局部免疫反应重新激活的观察,微生物介导的免疫治疗是下一代研究领域,其中免疫疗法经过工程化改造以克服免疫监视并逃逸微环境中的癌症防御。

我们的研究目的是在B16F10黑色素瘤肺转移的同源C57BL6小鼠模型中,评估鼻腔给予犬新孢子虫的潜力。研究还比较了野生型犬新孢子虫与分泌人白细胞介素(IL)-15(融合至IL-15受体α链sushi结构域,一种细胞免疫应答的强效激活剂)的犬新孢子虫的抗肿瘤特性。

通过鼻内给予一种经工程改造以分泌人 IL-15 的 N. caninum 治疗小鼠肺转移,可抑制肺转移进一步进展,肺表面仅有 0.08% 存在转移,而野生型 N. caninum 治疗小鼠为 4.4%,未治疗小鼠为 36%。对肿瘤发展的控制与肺内NK 细胞、CD8+ T 细胞和巨噬细胞数量显著增加相关,分别增加至两倍、五倍和六倍。对巨噬细胞表面 CD86 和 CD206 表达水平的分析显示,这些巨噬细胞向抗肿瘤 M1 表型极化。

展开英文摘要原文

Metastases are the leading cause of mortality in many cancer types and lungs are one of the most common sites of metastasis alongside the liver, brain, and bones. In melanoma, 85% of late-stage patients harbor lung metastases. A local administration could enhance the targeting of metastases while limiting the systemic cytotoxicity. Therefore, intranasal administration of immunotherapeutic agents seems to be a promising approach to preferentially target lung metastases and decrease their burden on cancer mortality. From observations that certain microorganisms induce an acute infection of the tumor microenvironment leading to a local reactivating immune response, microbial-mediated immunotherapy is a next-generation field of investigation in which immunotherapies are engineered to overcome immune surveillance and escape from microenvironmental cancer defenses.

The goal of our study is to evaluate the potential of the intranasal administration of Neospora caninum in a syngeneic C57BL6 mouse model of B16F10 melanoma lung metastases. It also compares the antitumoral properties of a wild-type N. caninum versus N. caninum secreting human interleukin (IL)-15 fused to the sushi domain of the IL-15 receptor α chain, a potent activator of cellular immune responses.

The treatment of murine lung metastases by intranasal administration of an N. caninum engineered to secrete human IL-15 impairs lung metastases from further progression with only 0,08% of lung surface harboring metastases versus 4,4% in wild-type N. caninum treated mice and 36% in untreated mice. The control of tumor development is associated with a strong increase in numbers, within the lung, of natural killer cells, CD8 + T cells and macrophages, up to twofold, fivefold and sixfold, respectively. Analysis of expression levels of CD86 and CD206 on macrophages surface revealed a polarization of these macrophages towards an antitumoral M1 phenotype.

Administration of IL-15/IL-15Rα-secreting N. caninum through intranasal administration, a non-invasive route, lend further support to N. caninum -demonstrated clear potential as an effective and safe immunotherapeutic approach for the treatment of metastatic solid cancers, whose existing therapeutic options are scarce. Combination of this armed protozoa with an intranasal route could reinforce the existing therapeutic arsenal against cancer and narrow the spectrum of incurable cancers.

论文信息

作者
Battistoni A、Lantier L、di Tommaso A、Ducournau C、Lajoie L、Samimi M、Coënon L、Rivière C
第一作者单位
Université de Tours, INRAE, ISP, F-37000, Faculté de pharmacie, Tours, France.France
通讯作者单位
Université de Tours, INRAE, ISP, F-37000, Faculté de pharmacie, Tours, France louis.lantier@univ-tours.fr.France
文献类型
非美国政府资助研究
期刊
Journal for immunotherapy of cancer2023 May
原文标识
PubMed 37192784 · DOI 10.1136/jitc-2023-006683