推进抗菌策略:crispr噬菌体介导的靶向细菌耐药基因的基因治疗。

IF 3.3 4区 医学 Q2 GENETICS & HEREDITY
Arvind Kumar Patel, Neha Singh, Neetu Sachan, Phool Chandra
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引用次数: 0

摘要

当今世界面临的最重要问题之一是抗生素耐药性,这使得治疗细菌感染变得越来越困难。常规抗生素不再对许多细菌起作用,影响了数百万人。一种被称为crispr噬菌体疗法的新方法可能是有益的。这项技术利用噬菌体将一种名为CRISPR的技术引入耐药细菌中。导致细菌对抗生素产生耐药性的基因可以通过CRISPR技术被识别和切断。这使得抗生素能够通过抑制细菌发挥作用。与传统抗生素不同,这种方法非常精确,因此不会损害我们体内的有益细菌。初步研究和有限的临床试验表明,这种技术可以有效地靶向耐药细菌,如肺炎克雷伯菌和耐甲氧西林金黄色葡萄球菌(MRSA)。然而,噬菌体工程、寄主递送和细菌CRISPR耐药性日益增长的威胁需要迫切和战略性的创新。我们的观点强调,如果不积极解决这些障碍,目前的希望可能会消失。展望未来,整合下一代Cas效应物、非dsb编辑器和耐药性监测框架可以将crispr噬菌体系统从实验新事物转变为临床支柱。这一转变不仅需要科学上的独创性,还需要在监管、转化和制造方面取得协调一致的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advancing Antibacterial Strategies: CRISPR-Phage-Mediated Gene Therapy Targeting Bacterial Resistance Genes.

One of the most significant issues facing the world today is antibiotic resistance, which makes it increasingly difficult to treat bacterial infections. Regular antibiotics no longer work against many bacteria, affecting millions of people. A novel approach known as CRISPR-phage therapy may be beneficial. This technique introduces a technology called CRISPR into resistant bacteria using bacteriophages. The genes that cause bacteria to become resistant to antibiotics can be identified and cut using CRISPR. This enables antibiotics to function by inhibiting the bacteria. This approach is highly precise, unlike conventional antibiotics, so it doesn't damage our bodies' beneficial bacteria. Preliminary studies and limited clinical trials suggest that this technique can effectively target drug-resistant bacteria such as Klebsiella pneumoniae and Methicillinresistant Staphylococcus aureus (MRSA). However, challenges in phage engineering, host delivery, and the growing threat of bacterial CRISPR resistance demand urgent and strategic innovation. Our perspective underscores that without proactive resolution of these hurdles, the current hopefulness could disappear. Looking ahead, integrating next-generation Cas effectors, non-DSB editors, and resistance monitoring frameworks could transform CRISPR-phage systems from an experimental novelty into a clinical mainstay. This shift will require not only scientific ingenuity but also coordinated advances in regulatory, translational, and manufacturing efforts.

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来源期刊
Current gene therapy
Current gene therapy 医学-遗传学
CiteScore
6.70
自引率
2.80%
发文量
46
期刊介绍: Current Gene Therapy is a bi-monthly peer-reviewed journal aimed at academic and industrial scientists with an interest in major topics concerning basic research and clinical applications of gene and cell therapy of diseases. Cell therapy manuscripts can also include application in diseases when cells have been genetically modified. Current Gene Therapy publishes full-length/mini reviews and original research on the latest developments in gene transfer and gene expression analysis, vector development, cellular genetic engineering, animal models and human clinical applications of gene and cell therapy for the treatment of diseases. Current Gene Therapy publishes reviews and original research containing experimental data on gene and cell therapy. The journal also includes manuscripts on technological advances, ethical and regulatory considerations of gene and cell therapy. Reviews should provide the reader with a comprehensive assessment of any area of experimental biology applied to molecular medicine that is not only of significance within a particular field of gene therapy and cell therapy but also of interest to investigators in other fields. Authors are encouraged to provide their own assessment and vision for future advances. Reviews are also welcome on late breaking discoveries on which substantial literature has not yet been amassed. Such reviews provide a forum for sharply focused topics of recent experimental investigations in gene therapy primarily to make these results accessible to both clinical and basic researchers. Manuscripts containing experimental data should be original data, not previously published.
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