Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10963542 | Vaccine | 2015 | 10 Pages |
Abstract
We developed a CTL vaccine vector by modification of the RPS-Vax system, a mucosal vaccine vector derived from a poliovirus Sabin 1 strain, and generated an oral CTL vaccine against HIV-1. A DNA fragment encoding a cytoplasmic transduction peptide (CTP) was integrated into the RPS-Vax system to generate RPS-CTP, a CTL vaccine vector. An HIV-1 p24 cDNA fragment was introduced into the RPS-CTP vector system and a recombinant poliovirus (rec-PV) named vRPS-CTP/p24 was produced. vRPS-CTP/p24 was genetically stable and efficiently induced Th1 immunity and p24-specific CTLs in immunized poliovirus receptor-transgenic (PVR-Tg) mice. In challenge experiments, PVR-Tg mice that were pre-immunized orally with vRPS-CTP/p24 were resistant to challenge with a lethal dose of p24-expressing recombinant vaccinia virus (rMVA-p24). These results suggested that the RPS-CTP vector system had potential for developing oral CTL vaccines against infectious diseases.
Keywords
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Immunology and Microbiology
Immunology
Authors
Seung-Soo Han, Jinjoo Lee, Yideul Jung, Myeong-Ho Kang, Jung-Hyub Hong, Min-Suk Cha, Yu-Jin Park, Ezra Lee, Cheol-Hee Yoon, Yong-Soo Bae,