Department of Biochemistry and Molecular Biology, Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC, Australia.
Front Immunol. 2021 Apr 22;12:645770. doi: 10.3389/fimmu.2021.645770. eCollection 2021.
Peptide vaccination remains a viable approach to induce T-cell mediated killing of tumors. To identify potential T-cell targets for Triple-Negative Breast Cancer (TNBC) vaccination, we examined the effect of the pro-inflammatory cytokine interferon-γ (IFNγ) on the transcriptome, proteome, and immunopeptidome of the TNBC cell line MDA-MB-231. Using high resolution mass spectrometry, we identified a total of 84,131 peptides from 9,647 source proteins presented by human leukocyte antigen (HLA)-I and HLA-II alleles. Treatment with IFNγ resulted in a remarkable remolding of the immunopeptidome, with only a 34% overlap between untreated and treated cells across the HLA-I immunopeptidome, and expression of HLA-II only detected on treated cells. IFNγ increased the overall number, diversity, and abundance of peptides contained within the immunopeptidome, as well increasing the coverage of individual source antigens. The suite of peptides displayed under conditions of IFNγ treatment included many known tumor associated antigens, with the HLA-II repertoire sampling 17 breast cancer associated antigens absent from those sampled by HLA-I molecules. Quantitative analysis of the transcriptome (10,248 transcripts) and proteome (6,783 proteins) of these cells revealed 229 common proteins and transcripts that were differentially expressed. Most of these represented downstream targets of IFNγ signaling including components of the antigen processing machinery such as tapasin and HLA molecules. However, these changes in protein expression did not explain the dramatic modulation of the immunopeptidome following IFNγ treatment. These results demonstrate the high degree of plasticity in the immunopeptidome of TNBC cells following cytokine stimulation and provide evidence that under pro-inflammatory conditions a greater variety of potential HLA-I and HLA-II vaccine targets are unveiled to the immune system. This has important implications for the development of personalized cancer vaccination strategies.
肽疫苗接种仍然是诱导 T 细胞介导的肿瘤杀伤的可行方法。为了鉴定三阴性乳腺癌 (TNBC) 疫苗接种的潜在 T 细胞靶点,我们研究了促炎细胞因子干扰素-γ (IFNγ) 对 TNBC 细胞系 MDA-MB-231 的转录组、蛋白质组和免疫肽组的影响。使用高分辨率质谱,我们从 HLA-I 和 HLA-II 等位基因呈递的 9647 个源蛋白中共鉴定了 84131 个肽。IFNγ 处理导致免疫肽组发生显著重塑,未经处理和处理细胞的 HLA-I 免疫肽组之间仅有 34%重叠,并且仅在处理细胞上检测到 HLA-II 表达。IFNγ 增加了免疫肽组中包含的肽的总数、多样性和丰度,并增加了个体源抗原的覆盖范围。在 IFNγ 处理条件下显示的肽套件包括许多已知的肿瘤相关抗原,而 HLA-II repertoire 采样了 17 个乳腺癌相关抗原,这些抗原未被 HLA-I 分子采样。对这些细胞的转录组 (10248 个转录本) 和蛋白质组 (6783 个蛋白质) 的定量分析显示 229 个共同的蛋白质和转录本存在差异表达。这些大多数是 IFNγ 信号转导的下游靶标,包括抗原加工机制的成分,如 tapasin 和 HLA 分子。然而,这些蛋白质表达的变化并不能解释 IFNγ 处理后免疫肽组的剧烈调节。这些结果表明,在细胞因子刺激下,TNBC 细胞的免疫肽组具有高度的可塑性,并提供了证据,即在促炎条件下,更多种类的潜在 HLA-I 和 HLA-II 疫苗靶点被揭示给免疫系统。这对个性化癌症疫苗接种策略的发展具有重要意义。