肿瘤和宿主微生物群对泌尿系统癌症免疫疗法反应的作用

Jake Drobner, Krishna Doppalapudi, B. Saraiya, V. Packiam, S. Ghodoussipour
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摘要

引言和目的:人们刚刚开始认识到微生物组在泌尿生殖系统恶性肿瘤的发展和治疗中的作用。越来越多的证据表明,微生物组可以通过高度动态的肿瘤微环境信号调节免疫疗法。然而,关于免疫肿瘤学-微生物组轴,尤其是在泌尿系统肿瘤学中,仍有许多未知之处。本综述旨在总结我们目前对微生物组在调节和预测泌尿生殖系统恶性肿瘤免疫疗法反应中的作用的理解:方法:我们检索了有关微生物组和膀胱癌、肾癌和前列腺癌免疫治疗反应的同行评审文献。对PubMed、Google Scholar、clinicaltrials.gov和bioRxiv上截至2023年9月的所有研究进行了分析:结果:与健康对照组相比,泌尿生殖系统癌症患者的尿液微生物群组成存在显著差异。乳酸生成菌,如双歧杆菌属和乳酸杆菌属,可能具有增强卡介苗对膀胱癌反应性的价值。卡介苗还可能是 PD-L1 的动态调节剂。因此,卡介苗与免疫检查点抑制剂的结合可能是治疗膀胱癌的有效策略。在晚期肾细胞癌中,研究表明近期服用抗生素会对接受免疫疗法的患者的生存结果产生负面影响,而服用 CBM588(一种活细菌产品)则与无进展生存期的改善有关。唾液链球菌等特定细菌类群与转移性耐阉割前列腺癌患者对 pembrolizumab 的反应有关。粪便微生物群移植已被证明可以克服免疫疗法的耐药性并降低毒性;目前正在对肾癌和前列腺癌进行研究:结论:虽然确切的机制尚不清楚,但多项研究确定了以微生物群为中心的干预措施与免疫疗法疗效之间的共生关系。利用微生物组改善泌尿生殖系统恶性肿瘤的免疫治疗反应性是可能的,但还需要采用更标准化的方法开展进一步研究。
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The Role of Tumor and Host Microbiome on Immunotherapy Response in Urologic Cancers
Introduction & Objective: The role of the microbiome in the development and treatment of genitourinary malignancies is just starting to be appreciated. Accumulating evidence suggests that the microbiome can modulate immunotherapy through signaling in the highly dynamic tumor microenvironment. Nevertheless, much is still unknown about the immuno-oncology-microbiome axis, especially in urologic oncology. The objective of this review is to synthesize our current understanding of the microbiome’s role in modulating and predicting immunotherapy response to genitourinary malignancies. Methods: A literature search for peer-reviewed publications about the microbiome and immunotherapy response in bladder, kidney, and prostate cancer was conducted. All research available in PubMed, Google Scholar, clinicaltrials.gov, and bioRxiv up to September 2023 was analyzed. Results: Significant differences in urinary microbiota composition have been found in patients with genitourinary cancers compared to healthy controls. Lactic acid-producing bacteria, such as Bifidobacterium and Lactobacillus genera, may have value in augmenting BCG responsiveness to bladder cancer. BCG may also be a dynamic regulator of PD-L1. Thus, the combination of BCG and immune checkpoint inhibitors may be an effective strategy for bladder cancer management. In advanced renal cell carcinoma, studies show that recent antibiotic administration negatively impacts survival outcomes in patients undergoing immunotherapy, while administration of CBM588, a live bacterial product, is associated with improved progression-free survival. Specific bacterial taxa, such as Streptococcus salivarius, have been linked with response to pembrolizumab in metastatic castrate-resistant prostate cancer. Fecal microbiota transplant has been shown to overcome resistance and reduce toxicity to immunotherapy; it is currently being investigated for both kidney and prostate cancers. Conclusions: Although the exact mechanism is unclear, several studies identify a symbiotic relationship between microbiota-centered interventions and immunotherapy efficacy. It is possible to improve immunotherapy responsiveness in genitourinary malignancies using the microbiome, but further research with more standardized methodology is warranted.
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