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一种基于腺病毒载体的呼吸道合胞病毒和带状疱疹候选疫苗的临床前开发

Pre-Clinical Development of an Adenovirus Vector Based RSV and Shingles Vaccine Candidate.

作者信息

Petherbridge Lawrence, Davis Charlotte, Robinson Angela, Evans Thomas, Sebastian Sarah

机构信息

Vaccitech Ltd., Harwell OX11 0DF, UK.

出版信息

Vaccines (Basel). 2023 Nov 2;11(11):1679. doi: 10.3390/vaccines11111679.

Abstract

Respiratory syncytial virus (RSV) infection and shingles are two viral diseases that affect older adults, and a combined vaccine to protect against both could be beneficial. RSV infection causes hospitalisations and significant morbidity in both children and adults and can be fatal in the elderly. The RSV fusion (F) envelope glycoprotein induces a strong RSV-neutralising antibody response and is the target of protective immunity in the first RSV vaccine for older adults, recently approved by the FDA. An initial childhood infection with the varicella zoster virus (VZV) results in chickenpox disease, but reactivation in older adults can cause shingles. This reactivation in sensory and autonomic neurons is characterized by a skin-blistering rash that can be accompanied by prolonged pain. The approved protein-in-adjuvant shingles vaccine induces VZV glycoprotein E (gE)-fspecific antibody and CD4 T cell responses and is highly effective. Here we report the evaluation of RSV/shingles combination vaccine candidates based on non-replicating chimpanzee adenovirus (ChAd) vectors. We confirmed the cellular and humoral immunogenicity of the vaccine vectors in mice using T cell and antibody assays. We also carried out an RSV challenge study in cotton rats which demonstrated protective efficacy following a homologous prime-boost regimen with our preferred vaccine candidate.

摘要

呼吸道合胞病毒(RSV)感染和带状疱疹是两种影响老年人的病毒性疾病,一种能同时预防这两种疾病的联合疫苗可能会有益处。RSV感染在儿童和成人中都会导致住院和显著的发病率,在老年人中可能是致命的。RSV融合(F)包膜糖蛋白可诱导强烈的RSV中和抗体反应,并且是美国食品药品监督管理局(FDA)最近批准的首款针对老年人的RSV疫苗中保护性免疫的靶点。初次感染水痘带状疱疹病毒(VZV)会导致水痘疾病,但在老年人中病毒再激活会引发带状疱疹。这种在感觉神经元和自主神经元中的再激活表现为伴有长时间疼痛的皮肤水疱疹。已获批的佐剂蛋白带状疱疹疫苗可诱导VZV糖蛋白E(gE)特异性抗体和CD4 T细胞反应,且非常有效。在此,我们报告了基于非复制型黑猩猩腺病毒(ChAd)载体的RSV/带状疱疹联合疫苗候选物的评估情况。我们通过T细胞和抗体检测在小鼠中确认了疫苗载体的细胞免疫原性和体液免疫原性。我们还在棉鼠中进行了RSV攻毒研究,结果表明,使用我们优选的疫苗候选物进行同源初免 - 加强免疫方案后具有保护效力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c47/10674764/95047d88a683/vaccines-11-01679-g001.jpg

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