推进噬菌体治疗:对细菌感染靶向治疗的安全性、有效性和未来前景的全面回顾。

IF 3.4 Q2 INFECTIOUS DISEASES
Marco Palma, Bowen Qi
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引用次数: 0

摘要

背景:噬菌体治疗是一种利用噬菌体对抗细菌感染的治疗方法,作为一种有希望的抗生素替代疗法,特别是在治疗耐药细菌方面,正受到人们的关注。本研究旨在从噬菌体治疗的安全性、有效性、影响因素、未来前景和监管考虑等方面对其进行综述。本研究还旨在确定优化其应用的策略,并为其临床实施提出系统的框架。方法:对临床前研究、临床试验和监管框架进行综合分析,以评估噬菌体疗法的治疗潜力。这包括对影响临床结果的关键因素的深入评估,如感染部位、噬菌体宿主特异性、细菌负担和免疫反应。此外,研究人员还探索了创新策略,如联合疗法、生物工程噬菌体和噬菌体鸡尾酒,以提高疗效。还研究了与剂量相关的关键因素,包括接种量、感染的多样性、治疗窗口和个性化医疗方法,以优化治疗结果。结果:噬菌体疗法在临床前和临床环境中都显示出良好的安全性,副作用最小。它能够特异性地针对有害细菌,同时保留有益微生物群,这巩固了它在治疗一系列感染方面的功效。然而,在一些研究中,不同的结果强调了解决影响治疗成功的关键因素的重要性。包括联合疗法、生物工程噬菌体、扩大获取各种噬菌体库、噬菌体鸡尾酒和个性化药物在内的创新方法,对提高疗效有着重大的希望。优化给药策略仍然是加强的关键领域,关键考虑因素包括接种量、感染的多样性、噬菌体动力学、耐药潜力、治疗窗口、给药频率和患者特异性因素。为了支持噬菌体治疗的临床应用,已经制定了一个简化的四步骤指南,为有效的治疗计划和实施提供了一个系统的框架。结论:噬菌体治疗为解决抗生素耐药感染提供了一种适应性强、针对性强、成本效益高的方法。虽然必须彻底评估几个关键因素以优化治疗效果,但通过创新策略和改进方法仍有很大的改进潜力。尽管噬菌体疗法尚未在美国和欧洲获得广泛批准,但通过扩大准入计划和FDA批准的食品病原体控制的可及性强调了其前景。波兰和格鲁吉亚等国的既定做法进一步证明了其临床可行性。为了实现更广泛的采用,生产、交付和质量控制方面的监管协调和进步将是必不可少的。值得注意的是,噬菌体治疗的可负担性和可扩展性使其成为发展中地区应对抗生素耐药性上升的特别有价值的解决方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advancing Phage Therapy: A Comprehensive Review of the Safety, Efficacy, and Future Prospects for the Targeted Treatment of Bacterial Infections.

Background: Phage therapy, a treatment utilizing bacteriophages to combat bacterial infections, is gaining attention as a promising alternative to antibiotics, particularly for managing antibiotic-resistant bacteria. This study aims to provide a comprehensive review of phage therapy by examining its safety, efficacy, influencing factors, future prospects, and regulatory considerations. The study also seeks to identify strategies for optimizing its application and to propose a systematic framework for its clinical implementation.

Methods: A comprehensive analysis of preclinical studies, clinical trials, and regulatory frameworks was undertaken to evaluate the therapeutic potential of phage therapy. This included an in-depth assessment of key factors influencing clinical outcomes, such as infection site, phage-host specificity, bacterial burden, and immune response. Additionally, innovative strategies-such as combination therapies, bioengineered phages, and phage cocktails-were explored to enhance efficacy. Critical considerations related to dosing, including inoculum size, multiplicity of infection, therapeutic windows, and personalized medicine approaches, were also examined to optimize treatment outcomes.

Results: Phage therapy has demonstrated a favorable safety profile in both preclinical and clinical settings, with minimal adverse effects. Its ability to specifically target harmful bacteria while preserving beneficial microbiota underpins its efficacy in treating a range of infections. However, variable outcomes in some studies highlight the importance of addressing critical factors that influence therapeutic success. Innovative approaches, including combination therapies, bioengineered phages, expanded access to diverse phage banks, phage cocktails, and personalized medicine, hold significant promise for improving efficacy. Optimizing dosing strategies remains a key area for enhancement, with critical considerations including inoculum size, multiplicity of infection, phage kinetics, resistance potential, therapeutic windows, dosing frequency, and patient-specific factors. To support the clinical application of phage therapy, a streamlined four-step guideline has been developed, providing a systematic framework for effective treatment planning and implementation.

Conclusion: Phage therapy offers a highly adaptable, targeted, and cost-effective approach to addressing antibiotic-resistant infections. While several critical factors must be thoroughly evaluated to optimize treatment efficacy, there remains significant potential for improvement through innovative strategies and refined methodologies. Although phage therapy has yet to achieve widespread approval in the U.S. and Europe, its accessibility through Expanded Access programs and FDA authorizations for food pathogen control underscores its promise. Established practices in countries such as Poland and Georgia further demonstrate its clinical feasibility. To enable broader adoption, regulatory harmonization and advancements in production, delivery, and quality control will be essential. Notably, the affordability and scalability of phage therapy position it as an especially valuable solution for developing regions grappling with escalating rates of antibiotic resistance.

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来源期刊
Infectious Disease Reports
Infectious Disease Reports INFECTIOUS DISEASES-
CiteScore
5.10
自引率
0.00%
发文量
82
审稿时长
11 weeks
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