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呼吸道合胞病毒疫苗研究的最新概况。

The recent landscape of RSV vaccine research.

作者信息

Kelleher Karen, Subramaniam Nadisha, Drysdale Simon B

机构信息

Oxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, UK.

NIHR Oxford Biomedical Research Centre, Oxford, UK.

出版信息

Ther Adv Vaccines Immunother. 2025 Jan 10;13:25151355241310601. doi: 10.1177/25151355241310601. eCollection 2025.

Abstract

Respiratory syncytial virus (RSV) causes a significant burden of acute respiratory illness across all ages, particularly for infants and older adults. Infants, especially those born prematurely or with underlying health conditions, face a high risk of severe RSV-related lower respiratory tract infections (LRTIs). Globally, RSV contributes to millions of LRTI cases annually, with a disproportionate burden in low- and middle-income countries (LMICs). The RSV virion outer capsule contains glycoproteins G and F which are essential for viral entry into respiratory epithelial cells and represent key targets for therapeutics development. The F-glycoprotein has several highly conserved antigenic sites that have proven useful targets for the development of monoclonal antibodies (mAbs) against RSV. Historically, prevention in infants was limited to the mAb palivizumab, which, despite its efficacy, was costly and inaccessible in many regions. Recent advancements include nirsevimab, a long-acting mAb that has shown substantial efficacy in reducing medically attended RSV-related disease in infants, in phase III clinical trials, early regional and national real-world data. In addition, three new vaccines have been approved: two protein subunit vaccines and a messenger RNA vaccine. The vaccines are all licenced for use in older adults, with one also approved as a maternal vaccine. Promising candidates in development include the mAb clesrovimab, which has an extended half-life and high levels in the nasal epithelial lining and high safety and efficacy profiles in late-stage trials. There are also a wide range of vaccine candidates currently in late-stage clinical trials. These developments signify a major advancement in RSV prevention strategies, offering improved protection for high-risk populations. With the ongoing rollout of the recently licenced vaccines and mAbs internationally, the landscape of RSV care is rapidly changing. We also must ensure these advances reach those in LMICs who need these therapies most.

摘要

呼吸道合胞病毒(RSV)在各年龄段都会引发严重的急性呼吸道疾病负担,对婴儿和老年人尤为如此。婴儿,尤其是早产或有基础健康问题的婴儿,面临着与RSV相关的严重下呼吸道感染(LRTIs)的高风险。在全球范围内,RSV每年导致数百万例LRTI病例,在低收入和中等收入国家(LMICs)负担尤为沉重。RSV病毒粒子的外囊膜含有糖蛋白G和F,它们对于病毒进入呼吸道上皮细胞至关重要,也是治疗药物开发的关键靶点。F糖蛋白有几个高度保守的抗原位点,已被证明是开发抗RSV单克隆抗体(mAbs)的有用靶点。从历史上看,婴儿预防措施仅限于单克隆抗体帕利珠单抗,尽管其有效,但在许多地区成本高昂且难以获得。最近的进展包括尼塞韦单抗,这是一种长效单克隆抗体,在III期临床试验、早期区域和国家真实世界数据中显示出在降低婴儿中因RSV相关疾病而就医方面有显著疗效。此外,三种新疫苗已获批准:两种蛋白亚单位疫苗和一种信使核糖核酸疫苗。这些疫苗均被许可用于老年人,其中一种还被批准作为母体疫苗。正在开发的有前景的候选药物包括单克隆抗体克塞罗单抗,它具有延长的半衰期,在鼻上皮衬里中含量高,在后期试验中具有高安全性和有效性。目前也有多种候选疫苗处于后期临床试验阶段。这些进展标志着RSV预防策略取得了重大进步,为高危人群提供了更好的保护。随着最近获批的疫苗和单克隆抗体在国际上的不断推广,RSV护理的格局正在迅速变化。我们还必须确保这些进展惠及最需要这些治疗的低收入和中等收入国家的人群。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43d2/11724408/c3fe88c9c783/10.1177_25151355241310601-fig1.jpg

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