Human cytomegalovirus: pathogenesis, prevention, and treatment.

IF 6.3 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular biomedicine Pub Date : 2024-11-25 DOI:10.1186/s43556-024-00226-7
Zifang Shang, Xin Li
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Abstract

Human cytomegalovirus (HCMV) infection remains a significant global health challenge, particularly for immunocompromised individuals and newborns. This comprehensive review synthesizes current knowledge on HCMV pathogenesis, prevention, and treatment strategies. We examine the molecular mechanisms of HCMV entry, focusing on the structure and function of key envelope glycoproteins (gB, gH/gL/gO, gH/gL/pUL128-131) and their interactions with cellular receptors such as PDGFRα, NRP2, and THBD. The review explores HCMV's sophisticated immune evasion strategies, including interference with pattern recognition receptor signaling, modulation of antigen presentation, and regulation of NK and T cell responses. We highlight recent advancements in developing neutralizing antibodies, various vaccine strategies (live-attenuated, subunit, vector-based, DNA, and mRNA), antiviral compounds (both virus-targeted and host-targeted), and emerging cellular therapies such as TCR-T cell approaches. By integrating insights from structural biology, immunology, and clinical research, we identify critical knowledge gaps and propose future research directions. This analysis aims to stimulate cross-disciplinary collaborations and accelerate the development of more effective prevention and treatment strategies for HCMV infections, addressing a significant unmet medical need.

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人类巨细胞病毒:发病机制、预防和治疗。
人类巨细胞病毒(HCMV)感染仍然是全球健康面临的重大挑战,尤其是对免疫力低下的人和新生儿而言。本综述综合了当前有关 HCMV 发病机制、预防和治疗策略的知识。我们研究了 HCMV 进入的分子机制,重点关注关键包膜糖蛋白(gB、gH/gL/gO、gH/gL/pUL128-131)的结构和功能,以及它们与细胞受体(如 PDGFRα、NRP2 和 THBD)的相互作用。本综述探讨了 HCMV 复杂的免疫逃避策略,包括干扰模式识别受体信号、调节抗原递呈以及调节 NK 和 T 细胞反应。我们重点介绍了在开发中和抗体、各种疫苗策略(减毒活疫苗、亚单位疫苗、载体疫苗、DNA 疫苗和 mRNA 疫苗)、抗病毒化合物(病毒靶向和宿主靶向)以及 TCR-T 细胞疗法等新兴细胞疗法方面的最新进展。通过整合结构生物学、免疫学和临床研究的见解,我们找出了关键的知识差距,并提出了未来的研究方向。这项分析旨在促进跨学科合作,加快开发更有效的 HCMV 感染预防和治疗策略,满足尚未得到满足的重大医疗需求。
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来源期刊
CiteScore
6.30
自引率
0.00%
发文量
0
审稿时长
10 weeks
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