Current progress in CRISPR-Cas systems for autoimmune diseases.

3区 生物学 Q2 Biochemistry, Genetics and Molecular Biology
Juveriya Israr, Ajay Kumar
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引用次数: 0

Abstract

A body develops an autoimmune illness when its immune system mistakenly targets healthy cells and organs. Eight million people are affected by more than 80 autoimmune diseases. The public's and individuals' well-being is put at risk. Type 1 diabetes, lupus, rheumatoid arthritis, and multiple sclerosisare autoimmune diseases. Tissue injury, nociceptive responses, and persistent inflammation are the results of these stresses. Concerns about healthcare costs, health, and physical limitations contribute to these issues. Given their prevalence, it is crucial to enhance our knowledge, conduct thorough research, and provide all-encompassing support to women dealing with autoimmune diseases. This will lead to better public health and better patient outcomes. Most bacteria's immune systems employ CRISPR-Cas, a state-of-the-art technique for editing genes. For Cas to break DNA with pinpoint accuracy, a guide RNA employs a predetermined enzymatic pathway. Genetic modifications started. After it was developed, this method was subjected to much research on autoimmune diseases. By modifying immune pathways, CRISPR gene editing can alleviate symptoms, promote immune system tolerance, and decrease autoimmune reactivity. The autoimmune diseases that CRISPR-Cas9 targets now have no treatment or cure. Results from early clinical trials and preclinical studies of autoimmune medicines engineered using CRISPR showed promise. Modern treatments for rheumatoid arthritis,multiple sclerosis, and type 1 diabetes aim to alter specific genetic or immune mechanisms. Accurate CRISPR editing can fix autoimmune genetic disorders. Modifying effector cells with CRISPR can decrease autoimmune reactions. These cells include cytotoxic T and B lymphocytes. Because of improvements in delivery techniques and kits, CRISPR medications are now safer, more effective, and more accurately targeted. It all comes down to intricate immunological reactions and unexpected side consequences. Revolutionary cures for autoimmune problems and highly personalized medical therapies have been made possible by recent advancements in CRISPR.

CRISPR-Cas 系统在治疗自身免疫性疾病方面的最新进展。
当人体的免疫系统错误地将健康细胞和器官作为攻击目标时,人体就会患上自身免疫性疾病。有 800 万人受到 80 多种自身免疫性疾病的影响。公众和个人的健康受到威胁。1 型糖尿病、红斑狼疮、类风湿性关节炎和多发性硬化症都是自身免疫性疾病。组织损伤、痛觉反应和持续炎症是这些压力的结果。人们对医疗费用、健康和身体限制的担忧也是造成这些问题的原因之一。鉴于这些问题的普遍性,我们必须加强了解、开展深入研究,并为患有自身免疫性疾病的妇女提供全方位的支持。这将提高公众健康水平,改善患者的治疗效果。大多数细菌的免疫系统都采用 CRISPR-Cas,这是一种最先进的基因编辑技术。为使Cas能准确无误地破坏DNA,引导RNA采用了预先确定的酶解途径。基因修改开始了。这种方法开发出来后,对自身免疫性疾病进行了大量研究。通过修改免疫途径,CRISPR 基因编辑可以缓解症状,促进免疫系统的耐受性,降低自身免疫反应性。CRISPR-Cas9所针对的自身免疫性疾病目前尚无治疗或治愈方法。利用CRISPR技术设计的自体免疫药物的早期临床试验和临床前研究结果表明,这种药物很有前景。类风湿性关节炎、多发性硬化症和 1 型糖尿病的现代疗法旨在改变特定的遗传或免疫机制。精确的CRISPR编辑可以修复自身免疫性遗传疾病。用CRISPR技术修改效应细胞可以减少自身免疫反应。这些细胞包括细胞毒性 T 淋巴细胞和 B 淋巴细胞。由于给药技术和试剂盒的改进,CRISPR 药物现在更安全、更有效、靶向性更准确。这一切都归结于错综复杂的免疫反应和意想不到的副作用。CRISPR技术的最新进展使自身免疫问题的革命性治疗和高度个性化的医疗疗法成为可能。
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
6.90
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Progress in Molecular Biology and Translational Science (PMBTS) provides in-depth reviews on topics of exceptional scientific importance. If today you read an Article or Letter in Nature or a Research Article or Report in Science reporting findings of exceptional importance, you likely will find comprehensive coverage of that research area in a future PMBTS volume.
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