Files

Download

Download Presentation Slides (511 KB)

Publication Date

10-5-2017

Description

Peptide or subunit vaccines (antigens) are safer than attenuated vaccines. However, peptide vaccines are less immunogenic and require large multiple doses of peptides plus exogenous adjuvants to elicit an immune response. The immunogenicity of peptide antigens can be enhanced if the peptides are immunized in the context of an antigen complex that mimics a virus in terms of size, morphology, and adjuvanticity. Virus-like particles (VLPs) derived from bacteriophages (PP7, MS2, and Qβ) possess these features and as such, they are excellent platforms for peptide vaccine designs. In this seminar, I will discuss how we have exploited these platforms to enhance the immunogenicity of less immunogenic but critical protective epitopes derived from viruses associated with pathogenic human infections such as human papillomaviruses, Zika virus, etc.

Disciplines

Biology

Vaccines against infectious agents

Included in

Biology Commons

Share

COinS
 
 

To view the content in your browser, please download Adobe Reader or, alternately,
you may Download the file to your hard drive.

NOTE: The latest versions of Adobe Reader do not support viewing PDF files within Firefox on Mac OS and if you are using a modern (Intel) Mac, there is no official plugin for viewing PDF files within the browser window.