Ziegler Stella, Bereswill Stefan, Heimesaat Markus M
Gastrointestinal Microbiology Research Group, Institute of Microbiology, Infectious Diseases and Immunology, Charité - University Medicine Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
Eur J Microbiol Immunol (Bp). 2022 Sep 23;12(3):63-72. doi: 10.1556/1886.2022.00017.
In line with the current development of individualized cancer treatments, targeted and specialized therapeutic regimens such as immunotherapy gain importance and factors improving its efficacy come into the focus of actual research. Given the orchestrated interaction of the intestinal microbiota with host immunity the modulation of the human gut microbiota represents a therapy-enhancing factor. We therefore performed an actual literature survey on the role of the gut microbiota composition and the effects of its modification during immunotherapy of cancer patients. The included 23 studies published in the past 10 years revealed that both, distinct bacterial species and genera including Faecalibacterium prausnitzii and Bifidobacterium, respectively, enhanced distinct immunotherapy responses following PD-1/PD-L1 and CTLA-4 blockage, for instance, resulting in a better clinical outcome of cancer patients. Conversely, a high intestinal abundance of Bacteroidetes and Fusobacterium species correlated with a less efficient immunotherapy resulting in shorter progress-free survival outcomes. In conclusion, modifications of the gut microbiota by fecal microbiota transplantation or application of probiotic compounds represent potential adjunct options for immunotherapy in cancer patients which needs to be further addressed in future trials to provide individually tailored and safe adjuvant therapeutic measures in the combat of cancer.
随着当前个性化癌症治疗的发展,免疫疗法等靶向和专门的治疗方案变得愈发重要,提高其疗效的因素成为实际研究的重点。鉴于肠道微生物群与宿主免疫的协同相互作用,调节人类肠道微生物群是一种增强治疗效果的因素。因此,我们对癌症患者免疫治疗期间肠道微生物群组成的作用及其改变的影响进行了实际文献调查。过去10年发表的23项纳入研究表明,不同的细菌种类和属,分别包括普拉梭菌和双歧杆菌,在PD-1/PD-L1和CTLA-4阻断后增强了不同的免疫治疗反应,例如,使癌症患者获得更好的临床结果。相反,拟杆菌属和梭杆菌属物种在肠道中的高丰度与免疫治疗效果较差相关,导致无进展生存期较短。总之,通过粪便微生物群移植或应用益生菌化合物对肠道微生物群进行改变,是癌症患者免疫治疗的潜在辅助选择,这需要在未来的试验中进一步探讨,以便在抗癌斗争中提供个性化定制且安全的辅助治疗措施。