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从新抗原发现到免疫检查点协同:肽癌症疫苗作为个性化癌症治疗的精准工具

英文原题:From Neoantigen Discovery to Immune-Checkpoint Synergy: Peptide Cancer Vaccines as Precision Tools for Personalised Cancer Therapy.

PubMed 2026/01/01(内容时间) Scand J Immunol Q3 · IF 2.4(JCR 2025)

研究概要

癌症的诊断、管理及潜在根除取决于肿瘤类型、分期、范围和解剖位置。

中文摘要

癌症的诊断、管理和潜在根除取决于肿瘤类型、分期、范围和解剖位置。虽然手术、化疗和放疗仍是核心手段,但分子肿瘤学的进展已将治疗转向个性化方法。肿瘤特异性分子异常和生物标志物的识别使得靶向治疗成为可能,这些治疗能够消除恶性细胞,同时限制对正常组织的损伤。癌症免疫治疗已成为一种有前景的非侵入性策略,可激活免疫系统识别并攻击肿瘤特异性抗原。基于减毒或灭活病毒的预防性疫苗在减少病毒相关癌症方面取得了显著成功。针对肿瘤相关抗原(TAAs)和患者特异性新抗原的治疗性疫苗旨在引发针对已形成肿瘤的强效细胞毒性和辅助性T细胞反应。基因组测序、生物信息学驱动的新抗原预测和单细胞分析方面的进展,如今使得肿瘤特异性靶点的准确识别成为可能。本综述重点介绍癌症疫苗研究的进展,聚焦于靶向TAAs、新抗原的策略以及递送平台,如基于树突细胞的系统、核酸疫苗(DNA和mRNA)、合成长肽和病毒或细菌载体。临床证据表明,新抗原疫苗可诱导强效的肿瘤特异性T细胞反应,且自身免疫性极小,并与免疫检查点抑制剂或使用TIL(肿瘤浸润淋巴细胞)(TILs)的过继性T细胞转移(ACT)联合使用时疗效增强。通过在肿瘤微环境中重新激活抗肿瘤T细胞,这些联合方法支持持久的肿瘤消退和改善的结局。尽管仍存在未解决的挑战,AI引导的靶点发现、基于纳米技术的递送系统以及可扩展制造方面的进展,为实现精准且持久的癌症治疗提供了有前景的解决方案。

展开英文摘要原文

The diagnosis, management and potential eradication of cancer depend on tumour type, stage, extent and anatomical location. While surgery, chemotherapy and radiotherapy remain central, advances in molecular oncology have shifted treatment toward personalised approaches. Identification of tumour-specific molecular abnormalities and biomarkers has enabled targeted therapies that eliminate malignant cells while limiting damage to normal tissues. Cancer immunotherapy has emerged as a promising, non-invasive strategy that activates the immune system to recognise and attack tumour-specific antigens. Preventive vaccines based on weakened or inactivated viruses have achieved notable success in reducing virus-associated cancers. Therapeutic vaccines targeting tumour-associated antigens (TAAs) and patient-specific neoantigens aim to elicit strong cytotoxic and helper T-cell responses against established tumours. Advances in genomic sequencing, bioinformatics-driven neoantigen prediction and single-cell profiling now enable accurate identification of tumour-specific targets. This review highlights progress in cancer vaccine research, focusing on strategies targeting TAAs, neoantigens and delivery platforms such as dendritic cell-based systems, nucleic acid vaccines (DNA and mRNA), synthetic long peptides and viral or bacterial vectors. Clinical evidence shows that neoantigen vaccines induce potent tumour-specific T-cell responses with minimal autoimmunity and gain enhanced efficacy when combined with immune checkpoint inhibitors or adoptive T-cell transfer (ACT) using tumour-infiltrating lymphocytes (TILs). By reinvigorating anti-tumour T cells within the tumour microenvironment, these combination approaches support durable tumour regression and improved outcomes. Despite unresolved challenges, advances in AI-guided target discovery, nanotechnology-based delivery systems and scalable manufacturing offer promising solutions for achieving precise and durable cancer treatment.

论文信息

作者
Banday AH、Manzoor MM、Nissar U、Jaleel S
第一作者单位
Department of Chemistry, Islamia College of Science and Commerce, Srinagar, India.India
通讯作者单位
Government Medical College Baramulla, Baramulla, Jammu and Kashmir, India.India
文献类型
综述
期刊
Scandinavian journal of immunology2026 Jan
原文标识
PubMed 41521168 · DOI 10.1111/sji.70084