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HXB2 Location | Env(35-49) gp120(35-49) DNA(6327..6371) |
Env Epitope Map |
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Author Location | Env | |
Epitope |
WVTVYYGVPVWKGAT
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Epitope Alignment
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Subtype | C | |
Species (MHC/HLA) | human | |
Immunogen | vaccine | |
Country | Switzerland | |
Experimental methods | CD8 T-cell Elispot - IFNγ, Other, Proliferation | |
Keywords | vaccine-induced immune responses, vaccine antigen design |
Vaccine type | vaccinia, modified vaccinia Ankara (MVA), poxvirus, DNA prime with poxvirus boost, attenuated poxvirus vector NYVAC |
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Vaccine strain | C clade 97CN54 |
Vaccine component | Env, Gag, Nef, Pol |
Harari2008 Alexandre Harari, Pierre-Alexandre Bart, Wolfgang Stöhr, Gonzalo Tapia, Miguel Garcia, Emmanuelle Medjitna-Rais, Séverine Burnet, Cristina Cellerai, Otto Erlwein, Tristan Barber, Christiane Moog, Peter Liljestrom, Ralf Wagner, Hans Wolf, Jean-Pierre Kraehenbuhl, Mariano Esteban, Jonathan Heeney, Marie-Joelle Frachette, James Tartaglia, Sheena McCormack, Abdel Babiker, Jonathan Weber, and Giuseppe Pantaleo. An HIV-1 Clade C DNA Prime, NYVAC Boost Vaccine Regimen Induces Reliable, Polyfunctional, and Long-Lasting T Cell Responses. J. Exp. Med., 205(1):63-77, 21 Jan 2008. PubMed ID: 18195071. Show all entries for this paper.
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