Guan Xiangyu, Bu Fanyu, Fu Yunyun, Zhang Haibo, Xiang Haitao, Chen Xinle, Chen Tai, Wu Xiaojian, Wu Kui, Liu Longqi, Dong Xuan
College of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
BGI Research, Hangzhou 310030, China.
iScience. 2024 Nov 9;27(12):111338. doi: 10.1016/j.isci.2024.111338. eCollection 2024 Dec 20.
Recent evidence has confirmed the presence of intratumor microbes, yet their impact on the immunopeptidome remains largely unexplored. Here we introduced an integrated strategy to identify the immunopeptidome originated from intratumor microbes. Analyzing 10 colorectal cancer (CRC) patients, we identified 154 putative microbe-derived human leukocyte antigen (HLA)-I ligands. Predominantly bacterial in origin, these peptides were notably abundant in , the most prevalent bacterium differentiating between normal and tumor tissues. We discovered 20 peptides originating from . , thirteen of which, including two peptides shared across multiple patients, were tumor specific. Validation experiments confirmed that the putative microbe-derived peptide could activate CD8 T cell responses. Our findings indicate that HLA-I molecules are capable of presenting intratumor microbe-derived peptides in CRC, potentially contributing to CD8 T cell-mediated immunity and suggesting potential strategies for cancer immunotherapy.
近期证据已证实肿瘤内微生物的存在,但其对免疫肽组的影响在很大程度上仍未得到探索。在此,我们引入了一种综合策略来鉴定源自肿瘤内微生物的免疫肽组。通过分析10例结直肠癌(CRC)患者,我们鉴定出154种假定的微生物来源的人类白细胞抗原(HLA)-I配体。这些肽主要来源于细菌,在 中显著丰富, 是区分正常组织和肿瘤组织的最普遍细菌。我们发现了20种源自 的肽。其中,13种,包括多名患者共有的两种肽,是肿瘤特异性的。验证实验证实,假定的微生物来源肽能够激活CD8 T细胞反应。我们的研究结果表明,HLA-I分子能够在CRC中呈递肿瘤内微生物来源的肽,可能有助于CD8 T细胞介导的免疫,并为癌症免疫治疗提出了潜在策略。