Control of a mucosal challenge and prevention of AIDS by a multiprotein DNA/MVA vaccine

被引:71
作者
Amara, RR
Villinger, F
Altman, JD
Lydy, SL
O'Neil, SP
Staprans, SI
Montefiori, DC
Xu, Y
Herndon, JG
Wyatt, LS
Candido, MA
Kozyr, NL
Earl, PL
Smith, JM
Ma, HL
Grimm, BD
Hulsey, ML
McClure, HM
McNicholl, JM
Moss, B
Robinson, HL
机构
[1] Emory Univ, Vaccine Res Ctr, Yerkes Reg Primate Res Ctr, Atlanta, GA 30329 USA
[2] Emory Univ, Sch Med, Vaccine Res Ctr, Dept Pathol & Lab Med, Atlanta, GA 30322 USA
[3] Emory Univ, Sch Med, Vaccine Res Ctr, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
[4] Duke Univ, Med Ctr, Dept Surg, Durham, NC 27710 USA
[5] NIAID, NIH, Viral Dis Lab, Bethesda, MD 20892 USA
[6] Emory Univ, Sch Med, Vaccine Res Ctr, Div Infect Dis,Dept Med, Atlanta, GA 30322 USA
[7] Natl Ctr Infect Dis, Div AIDS STD & TB Lab Res, Ctr Dis Control & Prevent, Atlanta, GA 30330 USA
关键词
mucosal challenged; multiprotein; heterologous prime; boost;
D O I
10.1016/S0264-410X(02)00076-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Heterologous prime/boost regimens have the potential for raising high levels of immune responses. Here, we report that DNA priming followed by a recombinant modified vaccinia Ankara (rMVA) booster has controlled a highly pathogenic immunodeficiency virus challenge in a Rhesus macaque model. Both the DNA and rMVA components of the vaccine expressed multiple immunodeficiency virus proteins. Two DNA inoculations at 0 and 8 weeks and a single rMVA booster at 24 weeks effectively controlled an intrarectal challenge administered 7 months after the booster. These highly promising findings provide hope that a relatively simple multiprotein DNA/MVA vaccine can help to control the AIDS epidemic. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1949 / 1955
页数:7
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