基于 DNA 超分子水凝胶的保护性 NK 细胞储库用于增强三阴性乳腺癌治疗
Protective NK Cell Reservoir Based on DNA Supramolecular Hydrogel for Enhanced Triple-Negative Breast Cancer Therapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Retrospective Analysis of HLA Class II-Restricted Neoantigen Peptide-Pulsed Dendritic Cell Vaccine for Breast Cancer.
Retrospective Analysis of HLA Class II-Restricted Neoantigen Peptide-Pulsed Dendritic Cell Vaccine for Breast Cancer.
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我们对乳腺癌组织进行了全外显子组和RNA测序,并使用计算机模拟流程进行新抗原预测。随后,我们将负载了合成的HLA II类限制性长肽(该长肽包含对HLA I类具有高亲和力的表位)的树突状细胞注射至淋巴结。
ELISPOT分析证实,所有病例均诱导了针对HLA II类限制性新抗原的特异性T细胞应答。对三例患者治疗前后外周血单个核细胞的TCR库分析显示,三例中有两例出现了特异性T细胞克隆的增加。重要的是,所有患者均未观察到复发。
我们的分析证明了HLA II类限制性新抗原肽树突状细胞疫苗对乳腺癌的免疫学疗效,并为乳腺癌新抗原疫苗治疗的开发提供了有用信息。
Background/Objectives : Neoantigens have attracted attention as ideal therapeutic targets for anti-tumour immunotherapy because the T cells that respond to neoantigens are not affected by central immune tolerance. Recent findings have revealed that the activation of CD4-positive T cells plays a central role in antitumor immunity, and thus targeting human leukocyte antigen (HLA) class II-restricted neoantigens, which are targets of CD4-positive T cells, is of significance.
However, there are very few detailed reports of neoantigen vaccine therapies that use an HLA class II-restricted long peptide. In the present study, we retrospectively analysed the ability of HLA class II-restricted neoantigen-pulsed dendritic cell vaccines to induce immune response in five breast cancer patients. Methods : We performed whole exome and RNA sequencing of breast cancer tissues and neoantigen prediction using an in silico pipeline.
We then administered dendritic cells pulsed with synthesized an HLA class II-restricted long peptide containing an epitope with high affinity to HLA class I in the lymph node. Results : ELISPOT analysis confirmed that a T-cell response specific for the HLA class II-restricted neoantigen was induced in all cases. TCR repertoire analysis of peripheral blood mononuclear cells before and after treatment in three patients showed increases of specific T-cell clones in two of the three patients.
Importantly, no recurrence was observed in all patients. Conclusions: Our analysis demonstrated the immunological efficacy of the HLA class II-restricted neoantigen peptide dendritic cell vaccine against breast cancer and provides useful information for the development of neoantigen vaccine therapy for breast cancer.
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