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本文引用的文献

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Neoadjuvant PD-1 Blockade in Resectable Lung Cancer.新辅助 PD-1 阻断治疗可切除性肺癌。
N Engl J Med. 2018 May 24;378(21):1976-1986. doi: 10.1056/NEJMoa1716078. Epub 2018 Apr 16.
2
ImmunoMap: A Bioinformatics Tool for T-cell Repertoire Analysis.免疫图谱:T 细胞受体谱分析的生物信息学工具。
Cancer Immunol Res. 2018 Feb;6(2):151-162. doi: 10.1158/2326-6066.CIR-17-0114. Epub 2017 Dec 20.
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Identifying specificity groups in the T cell receptor repertoire.识别T细胞受体库中的特异性组。
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Mismatch repair deficiency predicts response of solid tumors to PD-1 blockade.错配修复缺陷可预测实体瘤对程序性死亡受体1(PD-1)阻断疗法的反应。
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Evolution of Neoantigen Landscape during Immune Checkpoint Blockade in Non-Small Cell Lung Cancer.非小细胞肺癌免疫检查点阻断治疗期间新抗原格局的演变
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Discovery of T Cell Receptor β Motifs Specific to HLA-B27-Positive Ankylosing Spondylitis by Deep Repertoire Sequence Analysis.通过深度免疫受体谱序列分析发现 HLA-B27 阳性强直性脊柱炎的 T 细胞受体β基序。
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Tumor- and Neoantigen-Reactive T-cell Receptors Can Be Identified Based on Their Frequency in Fresh Tumor.肿瘤和新抗原反应性T细胞受体可根据其在新鲜肿瘤中的频率来识别。
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Targeting neoantigens for cancer immunotherapy.靶向新抗原用于癌症免疫治疗。
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9
Mechanism-driven biomarkers to guide immune checkpoint blockade in cancer therapy.用于指导癌症治疗中免疫检查点阻断的机制驱动生物标志物。
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10
Molecular basis for universal HLA-A*0201-restricted CD8+ T-cell immunity against influenza viruses.针对流感病毒的通用HLA-A*0201限制性CD8 + T细胞免疫的分子基础。
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突变相关新抗原功能扩展的特异性 T 细胞(MANAFEST)检测:一种用于监测抗肿瘤免疫的敏感平台。

The Mutation-Associated Neoantigen Functional Expansion of Specific T Cells (MANAFEST) Assay: A Sensitive Platform for Monitoring Antitumor Immunity.

机构信息

The Bloomberg-Kimmel Institute for Cancer Immunotherapy, Johns Hopkins University School of Medicine, Baltimore, Maryland.

The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, Maryland.

出版信息

Cancer Immunol Res. 2018 Aug;6(8):888-899. doi: 10.1158/2326-6066.CIR-18-0129. Epub 2018 Jun 12.

DOI:10.1158/2326-6066.CIR-18-0129
PMID:29895573
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6072595/
Abstract

Mutation-associated neoantigens (MANA) are a target of antitumor T-cell immunity. Sensitive, simple, and standardized assays are needed to assess the repertoire of functional MANA-specific T cells in oncology. Assays analyzing cytokine production such as ELISpot and intracellular cytokine staining have been useful but have limited sensitivity in assessing tumor-specific T-cell responses and do not analyze antigen-specific T-cell repertoires. The FEST (Functional Expansion of Specific T cells) assay described herein integrates T-cell receptor sequencing of short-term, peptide-stimulated cultures with a bioinformatic platform to identify antigen-specific clonotypic amplifications. This assay can be adapted for all types of antigens, including MANAs via tumor exome-guided prediction of MANAs. Following identification by the MANAFEST assay, the MANA-specific CDR3 sequence can be used as a molecular barcode to detect and monitor the dynamics of these clonotypes in blood, tumor, and normal tissue of patients receiving immunotherapy. MANAFEST is compatible with high-throughput routine clinical and lab practices. .

摘要

突变相关新抗原 (MANA) 是抗肿瘤 T 细胞免疫的靶点。需要敏感、简单和标准化的检测方法来评估肿瘤学中功能性 MANA 特异性 T 细胞的库。分析细胞因子产生的检测方法,如 ELISpot 和细胞内细胞因子染色,虽然有用,但在评估肿瘤特异性 T 细胞反应方面灵敏度有限,并且不分析抗原特异性 T 细胞库。本文所述的 FEST(特异性 T 细胞的功能扩增)检测方法将短期、肽刺激培养物的 T 细胞受体测序与生物信息学平台相结合,以鉴定抗原特异性克隆扩增。该检测方法可以适应所有类型的抗原,包括 MANA,通过肿瘤外显子组指导预测 MANA。在 MANAFEST 检测方法鉴定后,MANA 特异性 CDR3 序列可用作分子条码,以检测和监测接受免疫治疗的患者血液、肿瘤和正常组织中这些克隆型的动态。MANAFEST 与高通量常规临床和实验室实践兼容。