Jianan Psychiatric Center, Ministry of Health and Welfare, Tainan 71742, Taiwan.
Department of Mental Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA.
Int J Mol Sci. 2020 Feb 18;21(4):1376. doi: 10.3390/ijms21041376.
Cytomegalovirus (CMV) is one of the major human health threats worldwide, especially for immunologically comprised patients. CMV may cause opportunistic infections, congenital infections, and brain diseases (e.g., mental retardation and glioblastoma). The etiology of brain diseases associated with human CMV (HCMV) infections is usually complex and it is particularly difficult to treat because HCMV has a life-long infection in its hosts, high mutation rate, and latent infections. Moreover, it is almost impossible to eradicate latent viruses in humans. Although there has been progress in drug discovery recently, current drugs used for treating active CMV infections are still limited in efficacy due to side effects, toxicity, and viral resistance. Fortunately, letermovir which targets the HCMV terminase complex rather than DNA polymerase with fewer adverse reactions has been approved to treat CMV infections in humans. The researchers are focusing on developing approaches against both productive and latent infections of CMV. The gene or RNA targeting approaches including the external guide sequences (EGSs)-RNase, the clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) system and transcription activator-like effector nucleases (TALENs) are being investigated to remove acute and/or latent CMV infections. For the treatment of glioblastoma, vaccine therapy through targeting specific CMV antigens has improved patients' survival outcomes significantly and immunotherapy has also emerged as an alternative modality. The advanced research for developing anti-CMV agents and approaches is promising to obtain significant outcomes and expecting to have a great impact on the therapy of brain diseases associated with CMV infections.
巨细胞病毒(CMV)是全球主要的人类健康威胁之一,尤其对免疫功能受损的患者而言。CMV 可能导致机会性感染、先天性感染和脑部疾病(如智力障碍和神经胶质瘤)。与人类 CMV(HCMV)感染相关的脑部疾病的病因通常较为复杂,且治疗难度较大,原因在于 HCMV 在宿主中有终身感染、高突变率和潜伏感染。此外,在人类中几乎不可能根除潜伏病毒。尽管最近在药物发现方面取得了进展,但由于副作用、毒性和病毒耐药性,目前用于治疗活跃性 CMV 感染的药物在疗效上仍然有限。幸运的是,针对 HCMV 端粒酶复合物而非 DNA 聚合酶的药物 letermovir,因其不良反应较少而被批准用于治疗人类 CMV 感染。研究人员正专注于开发针对 CMV 生产性和潜伏性感染的方法。针对基因或 RNA 的方法,包括外部引导序列(EGS)-核糖核酸酶、成簇规律间隔短回文重复(CRISPR)/CRISPR 相关蛋白 9(Cas9)系统和转录激活因子样效应物核酸酶(TALENs),正被用于清除急性和/或潜伏性 CMV 感染。对于神经胶质瘤的治疗,通过针对特定 CMV 抗原的疫苗疗法显著改善了患者的生存结果,免疫疗法也已成为一种替代方法。开发抗 CMV 药物和方法的深入研究有望取得显著成果,并有望对 CMV 感染相关脑部疾病的治疗产生重大影响。