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巨细胞病毒疫苗的安全性、免疫原性和有效性:随机对照试验的系统评价

Safety, Immunogenicity, and Efficacy of Cytomegalovirus Vaccines: A Systematic Review of Randomized Controlled Trials.

作者信息

Chiavarini Manuela, Genga Anita, Ricciotti Giorgia Maria, D'Errico Marcello Mario, Barbadoro Pamela

机构信息

Department of Health Sciences, University of Florence, Viale GB Morgagni 48, 50134 Florence, Italy.

Department of Biomedical Sciences and Public Health, Section of Hygiene, Preventive Medicine and Public Health, Polytechnic University of the Marche Region, 60126 Ancona, Italy.

出版信息

Vaccines (Basel). 2025 Jan 17;13(1):85. doi: 10.3390/vaccines13010085.

Abstract

Cytomegalovirus (CMV) is widespread and mostly causes asymptomatic infections in immunocompetent hosts, but it may lead to severe and life-threatening diseases in immunocompromised individuals, such as transplant patients and congenitally infected children, representing a significant public health concern. Although there are no licensed CMV vaccines, the development of a CMV vaccine is considered a high priority due to its potential to reduce the burden associated with CMV-related complications, and several approaches are under investigation. The objective of this systematic review was to synthesize the evidence on various CMV vaccines currently under clinical development. : According to the PRISMA guidelines (PROSPERO ID: CRD42024516601), a comprehensive literature search was conducted to identify all the randomized controlled trials that have evaluated the safety, immunogenicity, and efficacy of vaccine candidates compared to a placebo. A total of 26 studies were identified: 11 on transplant patients and 15 on healthy individuals. : Several vaccine candidates have shown encouraging results in terms of safety and specific immune responses, notably adjuvanted gB vaccines and DNA vaccines targeting gB and pp65. The results were divided into RCTs on healthy individuals and those on transplant recipients, because the CMV-specific immune response to a vaccine is complex and varies depending not only on the type of vaccine, but also on the immunological status of the individual. : Challenges remain in achieving broad efficacy across diverse populations, particularly for immunocompromised patients. Thus, the present work seeks to support future decisions and guide further research in the development of an effective and widely available CMV vaccine.

摘要

巨细胞病毒(CMV)广泛传播,在免疫功能正常的宿主中大多引起无症状感染,但在免疫功能低下的个体中,如移植患者和先天性感染儿童,它可能导致严重的、危及生命的疾病,这是一个重大的公共卫生问题。尽管目前尚无获批的CMV疫苗,但由于其有可能减轻与CMV相关并发症相关的负担,CMV疫苗的研发被视为高度优先事项,目前有几种方法正在研究中。本系统评价的目的是综合目前正在临床开发的各种CMV疫苗的证据。:根据PRISMA指南(PROSPERO ID:CRD42024516601),进行了全面的文献检索,以确定所有评估候选疫苗与安慰剂相比的安全性、免疫原性和有效性的随机对照试验。共确定了26项研究:11项针对移植患者,15项针对健康个体。:几种候选疫苗在安全性和特异性免疫反应方面显示出令人鼓舞的结果,特别是佐剂gB疫苗以及针对gB和pp65的DNA疫苗。结果分为针对健康个体的随机对照试验和针对移植受者的随机对照试验,因为对疫苗的CMV特异性免疫反应很复杂,不仅取决于疫苗类型,还取决于个体的免疫状态。:在实现不同人群的广泛疗效方面仍然存在挑战,特别是对于免疫功能低下的患者。因此,本研究旨在支持未来的决策,并指导进一步研究开发一种有效且广泛可用的CMV疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8448/11768780/d29f745c5025/vaccines-13-00085-g001.jpg

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