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用于预防人类副流感病毒和呼吸道合胞病毒感染的重组仙台病毒疫苗的研发。

Development of recombinant Sendai virus vaccines for prevention of human parainfluenza and respiratory syncytial virus infections.

作者信息

Hurwitz Julia L

机构信息

Department of Infectious Diseases, St. Jude Children's Research Hospital, and Department of Pathology, University of Tennessee, Memphis, TN 38105, USA.

出版信息

Pediatr Infect Dis J. 2008 Oct;27(10 Suppl):S126-8. doi: 10.1097/INF.0b013e318168b780.

Abstract

Respiratory syncytial virus (RSV) and human parainfluenza viruses (hPIVs) are the most important causes of hospitalization for viral respiratory tract diseases in infants and young children. Unfortunately, there are currently no licensed vaccines for prevention of these infections. Researchers at St. Jude Children's Research Hospital are now developing Sendai virus (SV), a natural respiratory pathogen of mice, as a Jennerian vaccine for hPIV-1, and as a vaccine backbone for the prevention of RSV and other hPIVs. Unmodified SV is currently being tested in the clinic. Thus far, the vaccine has been well tolerated. Preclinical studies also continue and have demonstrated that intranasal vaccinations with recombinant SV expressing an RSV antigen are sufficient to activate high-magnitude RSV-specific neutralizing B- and T-cell activities in a cotton rat system. Furthermore, vaccinated animals are completely protected against RSV challenges. As clinical safety studies progress, St. Jude Children's Research Hospital researchers are also working to formulate a SV-based cocktail vaccine designed to prevent several hPIV and RSV infections in humans.

摘要

呼吸道合胞病毒(RSV)和人副流感病毒(hPIVs)是婴幼儿病毒性呼吸道疾病住院治疗的最重要病因。不幸的是,目前尚无预防这些感染的许可疫苗。圣犹大儿童研究医院的研究人员正在研发仙台病毒(SV),一种小鼠天然呼吸道病原体,作为hPIV-1的詹纳氏疫苗,以及预防RSV和其他hPIVs的疫苗主干。未修饰的SV目前正在临床中进行测试。到目前为止,该疫苗耐受性良好。临床前研究也在继续,并且已经证明,在棉鼠系统中,用表达RSV抗原的重组SV进行鼻内接种足以激活高强度的RSV特异性中和B细胞和T细胞活性。此外,接种疫苗的动物完全受到保护,免受RSV攻击。随着临床安全性研究的进展,圣犹大儿童研究医院的研究人员也在努力配制一种基于SV的联合疫苗,旨在预防人类的几种hPIV和RSV感染。

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