Vaccine-induced immunity in baboons by using DNA and replication-incompetent adenovirus type 5 vectors expressing a human immunodeficiency virus type 1 gag gene.

نویسندگان

  • Danilo R Casimiro
  • Aimin Tang
  • Ling Chen
  • Tong-Ming Fu
  • Robert K Evans
  • Mary-Ellen Davies
  • Daniel C Freed
  • William Hurni
  • Jose M Aste-Amezaga
  • Liming Guan
  • Romnie Long
  • Lingyi Huang
  • Virginia Harris
  • Denise K Nawrocki
  • Henryk Mach
  • Robert D Troutman
  • Lynne A Isopi
  • Krishna K Murthy
  • Karen Rice
  • Keith A Wilson
  • David B Volkin
  • Emilio A Emini
  • John W Shiver
چکیده

The cellular immunogenicity of formulated plasmid DNA and replication-defective human adenovirus serotype 5 (Ad5) vaccine vectors expressing a codon-optimized human immunodeficiency virus type 1 gag gene was examined in baboons. The Ad5 vaccine was capable of inducing consistently strong, long-lived CD8(+)-biased T-cell responses and in vitro cytotoxic activities. The DNA vaccine-elicited immune responses were weaker than those elicited by the Ad5 vaccine and highly variable; formulation with chemical adjuvants led to moderate increases in the levels of Gag-specific T cells. Increasing the DNA-primed responses with booster doses of either Ad5 or modified vaccinia virus Ankara vaccines suggests a difference in the relative levels of cytotoxic and helper responses. The implications of these results are discussed.

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عنوان ژورنال:
  • Journal of virology

دوره 77 13  شماره 

صفحات  -

تاریخ انتشار 2003