Zhao Yan, Wang Huaiyu
Department of Hematology, The First Affiliated Hospital of Xi'an Jiaotong University, 277 West Yanta Road, Xi'an, Shaanxi 710061, P.R. China.
Brief Bioinform. 2025 May 1;26(3). doi: 10.1093/bib/bbaf263.
Circular RNA (circRNA) vaccines have emerged as a groundbreaking innovation in infectious disease prevention and cancer immunotherapy, offering superior stability and reduced immunogenicity compared to conventional linear messenger RNA (mRNA) vaccines. While linear mRNA vaccines are prone to degradation and can trigger strong innate immune responses, covalently closed circRNA vaccines leverage their unique circular structure to enhance molecular stability and minimize innate immune activation, positioning them as a next-generation platform for vaccine development. Artificial intelligence (AI) is revolutionizing circRNA vaccine design and optimization. Deep learning models, such as convolutional neural networks (CNNs) and Transformers, integrate multi-omics data to refine antigen prediction, RNA secondary structure modeling, and lipid nanoparticle delivery system formulation, surpassing traditional bioinformatics approaches in both accuracy and efficiency. While AI-driven bioinformatics enhances antigen screening and delivery system modeling, generative AI accelerates literature synthesis and experimental planning-though the risk of fabricated references and limited biological interpretability hinders its reliability. Despite these advancements, challenges such as the "black-box" nature of AI algorithms, unreliable literature retrieval, and insufficient integration of biological mechanisms underscore the necessity for a hybrid "AI-traditional-experimental" paradigm. This approach integrates explainable AI frameworks, multi-omics validation, and ethical oversight to ensure clinical translatability. Future research should prioritize mechanism-driven AI models, real-time experimental feedback, and rigorous ethical standards to fully unlock the potential of circRNA vaccines in precision oncology and global health.
环状RNA(circRNA)疫苗已成为传染病预防和癌症免疫治疗领域的一项突破性创新,与传统的线性信使RNA(mRNA)疫苗相比,具有更高的稳定性和更低的免疫原性。线性mRNA疫苗容易降解,并能引发强烈的先天性免疫反应,而共价闭合的circRNA疫苗则利用其独特的环状结构来增强分子稳定性,并将先天性免疫激活降至最低,使其成为疫苗开发的下一代平台。人工智能(AI)正在彻底改变circRNA疫苗的设计和优化。深度学习模型,如卷积神经网络(CNN)和Transformer,整合多组学数据以优化抗原预测、RNA二级结构建模和脂质纳米颗粒递送系统配方,在准确性和效率方面都超过了传统的生物信息学方法。虽然人工智能驱动的生物信息学增强了抗原筛选和递送系统建模,但生成式人工智能加速了文献合成和实验规划——尽管存在虚假参考文献的风险和有限的生物学可解释性阻碍了其可靠性。尽管取得了这些进展,但诸如人工智能算法的“黑箱”性质、不可靠的文献检索以及生物机制整合不足等挑战凸显了混合“人工智能-传统-实验”范式的必要性。这种方法整合了可解释的人工智能框架、多组学验证和伦理监督,以确保临床可转化性。未来的研究应优先考虑机制驱动的人工智能模型、实时实验反馈和严格的伦理标准,以充分释放circRNA疫苗在精准肿瘤学和全球健康方面的潜力。