Bacterial mRNA Vaccines: Programming Immunity Against Antimicrobial Resistance

IF 4.2 4区 医学 Q2 CHEMISTRY, MEDICINAL
Rui Liao, Mingxing Luo, Fating Yang, Lifeng Xu, Jingjing Zhang, Weijun Zhang, Shan Guan, Yi Zhang, Ping Luo, Ping Cheng, Jing Yang, Yang Li, Qian Wang
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Abstract

The relentless rise of antimicrobial resistance poses a critical threat to global health, urgently demanding the development of antibacterial vaccines. Messenger RNA (mRNA) technology, validated during the COVID-19 pandemic, offers a powerful platform of fast development and flexibility. However, its application against bacterial pathogens remains an emerging frontier due to the structural complexity of bacterial antigens, challenges in achieving effective mucosal and cellular delivery, and the need to elicit balanced Th1/Th17-dominated immune responses for durable protection. Progress in antigen design, mRNA engineering, and lipid nanoparticle (LNP) delivery has enabled early preclinical success against Mycobacterium tuberculosis, Pseudomonas aeruginosa, and Streptococcus pneumoniae. Yet, challenges such as complex antigen expression, mucosal targeting, and immune durability persist. This review provides a brief overview of recent advances in bacterial mRNA vaccine design, including antigen selection, mRNA engineering, and delivery platform optimization. Additionally, we summarize current preclinical progress across key bacterial pathogens and highlight emerging strategies that integrate AI-guided antigen discovery, synthetic biology, and next-generation delivery systems to accelerate clinical translation. Finally, we highlight the prospects of bacterial mRNA vaccines by integrating synthetic biology, AI-driven antigen prediction, and advanced delivery systems. These cutting-edge technologies hold the promise of overcoming existing barriers, ultimately establishing mRNA vaccines as a viable and powerful strategy to curb the tide of antibiotic-resistant infections.

细菌mRNA疫苗:抗菌素耐药性编程免疫
抗菌素耐药性的持续上升对全球健康构成严重威胁,迫切需要开发抗菌疫苗。在2019冠状病毒病大流行期间得到验证的信使RNA (mRNA)技术提供了一个强大的快速开发和灵活性平台。然而,由于细菌抗原的结构复杂性,实现有效的粘膜和细胞递送的挑战,以及需要引起平衡的Th1/ th17主导的免疫反应以获得持久的保护,其对细菌病原体的应用仍然是一个新兴的前沿。抗原设计、mRNA工程和脂质纳米颗粒(LNP)递送方面的进展,使抗结核分枝杆菌、铜绿假单胞菌和肺炎链球菌的早期临床前成功。然而,诸如复杂抗原表达、粘膜靶向和免疫持久性等挑战仍然存在。本文综述了细菌mRNA疫苗设计的最新进展,包括抗原选择、mRNA工程和递送平台优化。此外,我们总结了目前主要细菌病原体的临床前进展,并强调了整合人工智能引导的抗原发现、合成生物学和下一代递送系统以加速临床转化的新兴策略。最后,我们通过整合合成生物学、人工智能驱动的抗原预测和先进的递送系统,强调了细菌mRNA疫苗的前景。这些尖端技术有望克服现有的障碍,最终使mRNA疫苗成为遏制抗生素耐药感染浪潮的一种可行而有力的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.40
自引率
2.60%
发文量
104
审稿时长
6-12 weeks
期刊介绍: Drug Development Research focuses on research topics related to the discovery and development of new therapeutic entities. The journal publishes original research articles on medicinal chemistry, pharmacology, biotechnology and biopharmaceuticals, toxicology, and drug delivery, formulation, and pharmacokinetics. The journal welcomes manuscripts on new compounds and technologies in all areas focused on human therapeutics, as well as global management, health care policy, and regulatory issues involving the drug discovery and development process. In addition to full-length articles, Drug Development Research publishes Brief Reports on important and timely new research findings, as well as in-depth review articles. The journal also features periodic special thematic issues devoted to specific compound classes, new technologies, and broad aspects of drug discovery and development.
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