Martin Spencer D, Brown Scott D, Wick Darin A, Nielsen Julie S, Kroeger David R, Twumasi-Boateng Kwame, Holt Robert A, Nelson Brad H
Trev and Joyce Deeley Research Centre, British Columbia Cancer Agency, Victoria, Canada.
Interdisciplinary Oncology Program, University of British Columbia, Vancouver, Canada.
PLoS One. 2016 May 18;11(5):e0155189. doi: 10.1371/journal.pone.0155189. eCollection 2016.
Due to advances in sequencing technology, somatically mutated cancer antigens, or neoantigens, are now readily identifiable and have become compelling targets for immunotherapy. In particular, neoantigen-targeted vaccines have shown promise in several pre-clinical and clinical studies. However, to date, neoantigen-targeted vaccine studies have involved tumors with exceptionally high mutation burdens. It remains unclear whether neoantigen-targeted vaccines will be broadly applicable to cancers with intermediate to low mutation burdens, such as ovarian cancer. To address this, we assessed whether a derivative of the murine ovarian tumor model ID8 could be targeted with neoantigen vaccines. We performed whole exome and transcriptome sequencing on ID8-G7 cells. We identified 92 somatic mutations, 39 of which were transcribed, missense mutations. For the 17 top predicted MHC class I binding mutations, we immunized mice subcutaneously with synthetic long peptide vaccines encoding the relevant mutation. Seven of 17 vaccines induced robust mutation-specific CD4 and/or CD8 T cell responses. However, none of the vaccines prolonged survival of tumor-bearing mice in either the prophylactic or therapeutic setting. Moreover, none of the neoantigen-specific T cell lines recognized ID8-G7 tumor cells in vitro, indicating that the corresponding mutations did not give rise to bonafide MHC-presented epitopes. Additionally, bioinformatic analysis of The Cancer Genome Atlas data revealed that only 12% (26/220) of HGSC cases had a ≥90% likelihood of harboring at least one authentic, naturally processed and presented neoantigen versus 51% (80/158) of lung cancers. Our findings highlight the limitations of applying neoantigen-targeted vaccines to tumor types with intermediate/low mutation burdens.
由于测序技术的进步,体细胞突变的癌症抗原,即新抗原,现在很容易识别,并已成为免疫治疗的诱人靶点。特别是,新抗原靶向疫苗在一些临床前和临床研究中显示出了前景。然而,迄今为止,新抗原靶向疫苗研究涉及的肿瘤具有极高的突变负担。新抗原靶向疫苗是否能广泛应用于中低突变负担的癌症,如卵巢癌,仍不清楚。为了解决这个问题,我们评估了小鼠卵巢肿瘤模型ID8的衍生物是否可以用新抗原疫苗靶向。我们对ID8-G7细胞进行了全外显子组和转录组测序。我们鉴定出92个体细胞突变,其中39个是转录的错义突变。对于17个预测的MHC I类结合突变中的前17个,我们用编码相关突变的合成长肽疫苗皮下免疫小鼠。17种疫苗中有7种诱导了强烈的突变特异性CD4和/或CD8 T细胞反应。然而,在预防或治疗环境中,没有一种疫苗能延长荷瘤小鼠的生存期。此外,没有一种新抗原特异性T细胞系在体外识别ID8-G7肿瘤细胞,这表明相应的突变没有产生真正的MHC呈递表位。此外,对癌症基因组图谱数据的生物信息学分析显示,只有12%(26/220)的高级别浆液性癌病例有≥90%的可能性携带至少一个真实的、自然加工和呈递的新抗原,而肺癌的这一比例为51%(80/158)。我们的研究结果突出了将新抗原靶向疫苗应用于中低突变负担肿瘤类型的局限性。