Modulation of the tumor microenvironment in non-muscle-invasive bladder cancer by OncoTherad® (MRB-CFI-1) nanoimmunotherapy: effects on tumor-associated macrophages, tumor-infiltrating lymphocytes, and monoamine oxidases.

IF 2.8 4区 医学 Q2 ONCOLOGY
Gabriela Cardoso de Arruda Camargo, Gabriela Oliveira, Bruna Nayara Silva Santos, Isadora Manzato Roberto, Monaliza Ávila, Bianca Ribeiro de Souza, João Carlos Cardoso Alonso, Nelson Durán, Wagner José Fávaro
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Abstract

Non-muscle-invasive bladder cancer (NMIBC) presents management challenges due to its high recurrence rate and a complex tumor microenvironment (TME). This study investigated the effects of OncoTherad® (MRB-CFI1) nanoimmunotherapy on the TME of BCG-unresponsive NMIBC, focusing on alterations in monoamine oxidases (MAO-A and MAO-B) and immune markers: CD163, FOXP3, CD8, and CX3CR1. A comparative analysis of immunoreactivities was made before and after OncoTherad® treatment and an immune score (IS) was established to evaluate the correlation between immunological changes and clinical outcomes. Forty bladder biopsies of twenty patients were divided into 2 groups (n = 20/group): 1 (pre-treatment biopsies); and 2 (post-treatment biopsies). Our results showed stable MAO-A levels but a significant (p < 0.05) decrease in MAO-B immunoreactivity after treatment, suggesting OncoTherad®'s efficacy in targeting the tumor-promoting and immunosuppressive functions of MAO-B. Significant (p < 0.05) reductions in CD163 and FOXP3 immunoreactivities were seen in post-treatment biopsies, indicating a decreased presence of M2 macrophages and Tregs. Corroborating with these results, we observed reductions in tumor histological grading, focality and size, factors that collectively enhanced recurrence-free survival (RFS) and pathological complete response (PCR). Moreover, elevated IFN-γ immunoreactivities in treated biopsies correlated with increased counts of CD8+ T cells and higher CX3CR1 expression, underscoring OncoTherad®'s enhancement of cytotoxic T cell functionality and overall antitumor immunity. The IS revealed improvements in immune responses post-treatment, with higher scores associated with better RFS and PCR outcomes. These findings validate OncoTherad®'s capability to modify the bladder cancer microenvironment favorably, promoting effective immune surveillance and response.

OncoTherad®(MRB-CFI-1)纳米免疫疗法对非肌层浸润性膀胱癌肿瘤微环境的调节:对肿瘤相关巨噬细胞、肿瘤浸润淋巴细胞和单胺氧化酶的影响。
非肌层浸润性膀胱癌(NMIBC)因其高复发率和复杂的肿瘤微环境(TME)而给治疗带来了挑战。本研究调查了 OncoTherad® (MRB-CFI1) 纳米免疫疗法对卡介苗无反应的非肌层浸润性膀胱癌 TME 的影响,重点关注单胺氧化酶(MAO-A 和 MAO-B)和免疫标记物的改变:CD163、FOXP3、CD8和CX3CR1。对 OncoTherad® 治疗前后的免疫活性进行了比较分析,并建立了免疫评分(IS),以评估免疫学变化与临床结果之间的相关性。将 20 名患者的 40 份膀胱活检样本分为 2 组(n = 20/组):1组(治疗前活检);2组(治疗后活检)。我们的研究结果表明,MAO-A 水平稳定,但 T 细胞(p +)显著增加,CX3CR1 表达更高,这表明 OncoTherad® 增强了细胞毒性 T 细胞的功能和整体抗肿瘤免疫力。IS显示治疗后免疫反应有所改善,得分越高,RFS和PCR结果越好。这些研究结果验证了 OncoTherad® 改变膀胱癌微环境、促进有效免疫监视和反应的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Medical Oncology
Medical Oncology 医学-肿瘤学
CiteScore
4.20
自引率
2.90%
发文量
259
审稿时长
1.4 months
期刊介绍: Medical Oncology (MO) communicates the results of clinical and experimental research in oncology and hematology, particularly experimental therapeutics within the fields of immunotherapy and chemotherapy. It also provides state-of-the-art reviews on clinical and experimental therapies. Topics covered include immunobiology, pathogenesis, and treatment of malignant tumors.
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