作者
Lan Zhang, Eberhard Durr, Jennifer D Galli, Scott Cosmi, Pedro J Cejas, Bin Luo, Sinoeun Touch, Paul Parmet, Arthur Fridman, Amy S Espeseth, Andrew J Bett
发表日期
2018/12/18
期刊
Vaccine
卷号
36
期号
52
页码范围
8119-8130
出版商
Elsevier
简介
Respiratory Syncytial Virus (RSV) infection is the leading cause of lower respiratory tract infection in both young children and older adults. Currently, there is no licensed vaccine available, and therapeutic options are limited. The infectious RSV particle is decorated with a type I viral fusion (F) glycoprotein that structurally rearranges from a metastable prefusion form to a highly stable postfusion form. In people naturally infected with RSV, the neutralizing antibodies primarily recognize the prefusion conformation. Therefore, engineered RSV F protein stabilized in its prefusion conformation has been an attractive strategy for developing RSV F vaccine antigens. Long-term stability at 4 °C or higher is a desirable attribute for a RSV F subunit vaccine antigen. We have previously shown that a prefusion stabilized RSV F construct, DS-Cav1, undergoes conformational changes and forms intermediate structures upon long …
引用总数
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