The Institute of Chemical Biology and Fundamental Medicine, Siberian Branch, Russian Academy of Sciences, Novosibirsk 630090, Russia.
Int J Mol Sci. 2023 Dec 26;25(1):334. doi: 10.3390/ijms25010334.
Hepatitis is an inflammatory liver disease primarily caused by hepatitis A (HAV), B (HBV), C (HCV), D (HDV), and E (HEV) viruses. The chronic forms of hepatitis resulting from HBV and HCV infections can progress to cirrhosis or hepatocellular carcinoma (HCC), while acute hepatitis can lead to acute liver failure, sometimes resulting in fatality. Viral hepatitis was responsible for over 1 million reported deaths annually. The treatment of hepatitis caused by viral infections currently involves the use of interferon-α (IFN-α), nucleoside inhibitors, and reverse transcriptase inhibitors (for HBV). However, these methods do not always lead to a complete cure for viral infections, and chronic forms of the disease pose significant treatment challenges. These facts underscore the urgent need to explore novel drug developments for the treatment of viral hepatitis. The discovery of the CRISPR/Cas9 system and the subsequent development of various modifications of this system have represented a groundbreaking advance in the quest for innovative strategies in the treatment of viral infections. This technology enables the targeted disruption of specific regions of the genome of infectious agents or the direct manipulation of cellular factors involved in viral replication by introducing a double-strand DNA break, which is targeted by guide RNA (spacer). This review provides a comprehensive summary of our current knowledge regarding the application of the CRISPR/Cas system in the regulation of viral infections caused by HAV, HBV, and HCV. It also highlights new strategies for drug development aimed at addressing both acute and chronic forms of viral hepatitis.
肝炎是一种肝脏炎症疾病,主要由甲型肝炎(HAV)、乙型肝炎(HBV)、丙型肝炎(HCV)、丁型肝炎(HDV)和戊型肝炎(HEV)病毒引起。由 HBV 和 HCV 感染引起的慢性肝炎可进展为肝硬化或肝细胞癌(HCC),而急性肝炎可导致急性肝功能衰竭,有时导致死亡。病毒性肝炎每年导致超过 100 万人死亡。目前,病毒感染引起的肝炎的治疗方法包括使用干扰素-α(IFN-α)、核苷抑制剂和逆转录酶抑制剂(用于 HBV)。然而,这些方法并不总是能完全治愈病毒感染,慢性肝炎形式带来了重大的治疗挑战。这些事实突显了迫切需要探索治疗病毒性肝炎的新药开发。CRISPR/Cas9 系统的发现以及对该系统的各种改进的开发代表了在寻求治疗病毒感染的创新策略方面的突破性进展。该技术可通过引入双链 DNA 断裂(靶向由向导 RNA(间隔子))来靶向破坏传染性病原体基因组的特定区域或直接操纵参与病毒复制的细胞因子。本综述全面总结了我们目前对 CRISPR/Cas 系统在调节 HAV、HBV 和 HCV 引起的病毒感染中的应用的认识。它还强调了针对急性和慢性病毒性肝炎的新药物开发策略。