Potent, protective anti-HIV immune responses generated by bimodal HIV envelope DNA pins protein vaccination

被引:281
作者
Letvin, NL
Montefiori, DC
Yasutomi, Y
Perry, HC
Davies, ME
Lekutis, C
Alroy, M
Freed, DC
Lord, CI
Handt, LK
Liu, MA
Shiver, JW
机构
[1] DUKE UNIV,MED CTR,DEPT SURG,DURHAM,NC 27710
[2] HARVARD UNIV,BETH ISRAEL HOSP,SCH MED,BOSTON,MA 02215
[3] MERCK RES LABS,DEPT VIRUS & CELL BIOL,W POINT,PA 19486
关键词
CTL; virus neutralization; vaccine; SHIV; T lymphocyte;
D O I
10.1073/pnas.94.17.9378
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
It is generally thought that an effective vaccine to prevent HIV-1 infection should elicit both strong neutralizing antibody and cytotoxic T lymphocyte responses, We recently demonstrated that potent, boostable, long-lived HIV-1 envelope (Env)-specific cytotoxic T lymphocyte responses can be elicited in rhesus monkeys using plasmid-encoded HIV-1 env DNA as the immunogen, In the present study, we show that the addition of HIV-I Env protein to this regimen as a boosting immunogen generates a high titer neutralizing antibody response in this nonhuman primate species, Moreover, we demonstrate in a pilot study that immunization with HIV-1 env DNA (multiple doses) followed by a final immunization with HIV-1 env DNA plus HIV-1 Env protein (env gene from HXBc2 clone of HIV IIIB; Env protein from parental HIV IIIB) completely protects monkeys from infection after i.v. challenge with a chimeric virus expressing HIV-1 env (HXBc2) on a simian immunodeficiency virus(mac) backbone (SHIV-HXBc2). The potent immunity and protection seen in these pilot experiments suggest that a DNA prime/DNA plus protein boost regimen warrants active investigation as a vaccine strategy to prevent HIV-1 infection.
引用
收藏
页码:9378 / 9383
页数:6
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