Terán-Navarro Hector, Zeoli Andrea, Salines-Cuevas David, Marradi Marco, Montoya Noemi, Gonzalez-Lopez Elena, Ocejo-Vinyals Javier Gonzalo, Dominguez-Esteban Mario, Gutierrez-Baños Jose Luis, Campos-Juanatey Felix, Yañez-Diaz Sonsoles, Garcia-Castaño Almudena, Rivera Fernando, Duran Ignacio, Alvarez-Dominguez Carmen
Grupo de Oncología y Nanovacunas, Instituto de Investigación Marqués de Valdecilla (IDIVAL), 39011 Santander, Cantabria, Spain.
Dipartimento di Chimica "Ugo Schiff", Universitá Degli Studi di Firenze, I-50019 Firenze, Italy.
Cancers (Basel). 2022 May 13;14(10):2413. doi: 10.3390/cancers14102413.
This study presents proof of concept assays to validate gold nanoparticles loaded with the bacterial peptide 91-99 of the listeriolysin O toxin (GNP-LLO nanovaccines) as immunotherapy for bladder tumors. GNP-LLO nanovaccines showed adjuvant abilities as they induce maturation and activation of monocyte-derived dendritic cells (MoDCs) to functional antigen-presenting cells in healthy donors and patients with melanoma or bladder cancer (BC), promoting a Th1 cytokine pattern. GNP-LLO nanovaccines were also efficient dendritic cell inducers of immunogenic tumor death using different bladder and melanoma tumor cell lines. The establishment of a pre-clinical mice model of subcutaneous BC confirmed that a single dose of GNP-LLO nanovaccines reduced tumor burden 4.7-fold and stimulated systemic Th1-type immune responses. Proof of concept assays validated GNP-LLO nanovaccines as immunotherapy by comparison to anti-CTLA-4 or anti-PD-1 antibodies. In fact, GNP-LLO nanovaccines increased percentages of CD4 and CD8 T cells, B cells, and functional antigen-presenting DCs in tumor-infiltrated lymphocytes, while they reduced the levels of myeloid-derived suppressor cells (MDSC) and suppressor T cells (T). We conclude that GNP-LLO nanovaccines can work as monotherapies or combinatory immunotherapies with anti-CTLA-4 or anti-PD-1 antibodies for solid tumors with high T cell infiltration, such as bladder cancer or melanoma.
本研究提供了概念验证试验,以验证负载李斯特菌溶血素O毒素细菌肽91-99的金纳米颗粒(GNP-LLO纳米疫苗)作为膀胱肿瘤免疫疗法的有效性。GNP-LLO纳米疫苗具有佐剂能力,因为它们可诱导健康供体以及黑色素瘤或膀胱癌(BC)患者的单核细胞衍生树突状细胞(MoDC)成熟并激活为功能性抗原呈递细胞,促进Th1细胞因子模式。使用不同的膀胱和黑色素瘤肿瘤细胞系,GNP-LLO纳米疫苗也是免疫原性肿瘤死亡的有效树突状细胞诱导剂。皮下BC临床前小鼠模型的建立证实,单剂量的GNP-LLO纳米疫苗可使肿瘤负担降低4.7倍,并刺激全身性Th1型免疫反应。与抗CTLA-4或抗PD-1抗体相比,概念验证试验验证了GNP-LLO纳米疫苗作为免疫疗法的有效性。事实上,GNP-LLO纳米疫苗增加了肿瘤浸润淋巴细胞中CD4和CD8 T细胞、B细胞以及功能性抗原呈递DC的百分比,同时降低了髓系来源抑制细胞(MDSC)和抑制性T细胞(T)的水平。我们得出结论,GNP-LLO纳米疫苗可作为单一疗法或与抗CTLA-4或抗PD-1抗体联合用于高T细胞浸润的实体瘤,如膀胱癌或黑色素瘤的免疫疗法。