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表达呼吸道病毒包膜糖蛋白的仙台病毒载体疫苗。

Sendai Virus-Vectored Vaccines That Express Envelope Glycoproteins of Respiratory Viruses.

机构信息

Department of Infectious Diseases, St. Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, TN 38105-3678, USA.

出版信息

Viruses. 2021 May 29;13(6):1023. doi: 10.3390/v13061023.

DOI:10.3390/v13061023
PMID:34072332
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8230104/
Abstract

Human respiratory syncytial virus (HRSV), human metapneumovirus (HMPV), and human parainfluenza viruses (HPIVs) are leading causes of respiratory disease in young children, the elderly, and individuals of all ages with immunosuppression. Vaccination strategies against these pneumoviruses and paramyxoviruses are vast in number, yet no licensed vaccines are available. Here, we review development of Sendai virus (SeV), a versatile pediatric vaccine that can (a) serve as a Jennerian vaccine against HPIV1, (b) serve as a recombinant vaccine against HRSV, HPIV2, HPIV3, and HMPV, (c) accommodate foreign genes for viral glycoproteins in multiple intergenic positions, (d) induce durable, mucosal, B-cell, and T-cell immune responses without enhanced immunopathology, (e) protect cotton rats, African green monkeys, and chimpanzees from infection, and (f) be formulated into a vaccine cocktail. Clinical phase I safety trials of SeV have been completed in adults and 3-6-year-old children. Clinical testing of SeVRSV, an HRSV fusion (F) glycoprotein gene recombinant, has also been completed in adults. Positive results from these studies, and collaborative efforts with the National Institutes of Health and the Serum Institute of India assist advanced development of SeV-based vaccines. Prospects are now good for vaccine successes in infants and consequent protection against serious viral disease.

摘要

人类呼吸道合胞病毒(HRSV)、人类偏肺病毒(HMPV)和人类副流感病毒(HPIVs)是导致婴幼儿、老年人和所有年龄段免疫抑制人群呼吸道疾病的主要原因。针对这些肺炎病毒和副粘病毒的疫苗接种策略很多,但目前尚无获得许可的疫苗。在这里,我们回顾了仙台病毒(SeV)的开发情况,仙台病毒是一种多功能的儿科疫苗,它可以(a)作为预防 HPIV1 的 Jennerian 疫苗,(b)作为预防 HRSV、HPIV2、HPIV3 和 HMPV 的重组疫苗,(c)在多个基因间位置容纳针对病毒糖蛋白的外源基因,(d)诱导持久的黏膜、B 细胞和 T 细胞免疫反应,而不会增强免疫病理学,(e)保护棉鼠、非洲绿猴和黑猩猩免受感染,(f)可制成疫苗鸡尾酒。已经在成年人和 3-6 岁儿童中完成了 SeV 的 I 期临床安全性试验。针对 HRSV 融合(F)糖蛋白基因重组的 SeVRSV 的临床测试也已经在成年人中完成。这些研究的积极结果,以及与美国国立卫生研究院和印度血清研究所的合作,有助于推进基于 SeV 的疫苗的研发。现在,在婴儿中成功开发疫苗并预防严重病毒性疾病的前景很好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c04/8230104/fcf82535d043/viruses-13-01023-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c04/8230104/167135a1bfb3/viruses-13-01023-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c04/8230104/179be69fc519/viruses-13-01023-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c04/8230104/35d4bfbe920b/viruses-13-01023-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c04/8230104/3f02dc534eb0/viruses-13-01023-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c04/8230104/67a8b54e1cad/viruses-13-01023-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c04/8230104/fcf82535d043/viruses-13-01023-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c04/8230104/167135a1bfb3/viruses-13-01023-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c04/8230104/179be69fc519/viruses-13-01023-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c04/8230104/35d4bfbe920b/viruses-13-01023-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c04/8230104/3f02dc534eb0/viruses-13-01023-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c04/8230104/67a8b54e1cad/viruses-13-01023-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c04/8230104/fcf82535d043/viruses-13-01023-g006.jpg

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