Journal article
Prefusion F-Based Polyanhydride Nanovaccine Induces Both Humoral and Cell-Mediated Immunity Resulting in Long-Lasting Protection against Respiratory Syncytial Virus
The Journal of immunology (1950), Vol.206(9), pp.2122-2134
05/01/2021
DOI: 10.4049/jimmunol.2100018
PMCID: PMC8062305
PMID: 33827894
Abstract
Respiratory syncytial virus (RSV) is a leading cause of lower respiratory tract infection in both young children and in older adults. Despite the morbidity, mortality, and high economic burden caused by RSV worldwide, no licensed vaccine is currently available. We have developed a novel RSV vaccine composed of a prefusion-stabilized variant of the fusion (F) protein (DS-Cav1) and a CpG oligodeoxynucleotide adjuvant encapsulated within polyanhydride nanoparticles, termed RSVNanoVax. A prime-boost intranasal administration of RSVNanoVax in BALB/c mice significantly alleviated weight loss and pulmonary dysfunction in response to an RSV challenge, with protection maintained up to at least 6 mo postvaccination. In addition, vaccinated mice exhibited rapid viral clearance in the lungs as early as 2 d after RSV infection in both inbred and outbred populations. Vaccination induced tissue-resident memory CD4 and CD8 T cells in the lungs, as well as RSV F-directed neutralizing Abs. Based on the robust immune response elicited and the high level of durable protection observed, our prefusion RSV F nanovaccine is a promising new RSV vaccine candidate.
Details
- Title: Subtitle
- Prefusion F-Based Polyanhydride Nanovaccine Induces Both Humoral and Cell-Mediated Immunity Resulting in Long-Lasting Protection against Respiratory Syncytial Virus
- Creators
- Laura M Stephens - University of IowaKathleen A Ross - Iowa State UniversityKody A Waldstein - University of IowaKevin L Legge - University of IowaJason S McLellan - The University of Texas at AustinBalaji Narasimhan - Iowa State UniversitySteven M Varga - University of Iowa
- Resource Type
- Journal article
- Publication Details
- The Journal of immunology (1950), Vol.206(9), pp.2122-2134
- DOI
- 10.4049/jimmunol.2100018
- PMID
- 33827894
- PMCID
- PMC8062305
- NLM abbreviation
- J Immunol
- ISSN
- 0022-1767
- eISSN
- 1550-6606
- Grant note
- T32 AI007485 / NIAID NIH HHS R01 AI124093 / NIAID NIH HHS T32 CA078586 / NCI NIH HHS
- Language
- English
- Date published
- 05/01/2021
- Academic Unit
- Graduate College Admin and Gen; Microbiology and Immunology; Pathology; Otolaryngology
- Record Identifier
- 9984186550902771
Metrics
16 Record Views