HIV-1 prophylactic vaccine comprised of topical DermaVir prime and protein boost elicits cellular immune responses and controls pathogenic R5 SHIV162P3

被引:32
作者
Cristillo, Anthony D.
Lisziewicz, Julianna
He, Leilei
Lori, Franco
Galmin, Lindsey
Trocio, Jeffrey N.
Unangst, Tami
Whitman, Lucia
Hudacik, Lauren
Bakare, Nyasha
Whitney, Stephen
Restrepo, Susana
Suschak, John
Ferrari, Maria Grazi
Chung, H. K.
Kalyanaraman, Vaniambadi S.
Markham, Phillip
Pal, Ranajit
机构
[1] Adv BioSci Labs Inc, Kensington, NSW 20895, Australia
[2] Genet Immunity, Mclean, VA 22102 USA
[3] IRCCS, Res Inst Human & Genet Theraphy, Policlin San Matteo, Pavia, Italy
关键词
HIV-1; vaccine; AIDS; cellular immune response; T cell memory;
D O I
10.1016/j.virol.2007.04.012
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Topical DNA vaccination (DermaVir) facilitates antigen presentation to naive T cells. DermaVir immunization in mice, using HIV-1 Env and Gag, elicited cellular immune responses. Boosting with HIV-1 gp120 Env and p41 Gag augmented Th1 cytokine levels. Intramuscular DNA administration was less efficient in priming antigen-specific cytokine production and memory T cells. In rhesus macaques, DermaVir immunization induced Gag- and Env-specific Th1 and Th2 cytokines and generation of memory T cells. Boosting of DennaVir-primed serum antibody levels was noted following gp140(SHIV89.6P)/p27(SIV) immunization. Rectal challenge with pathogenic R5-tropic SHIV162P3 resulted in control of plasma viremia (4/5 animals) that was reflected in jejunum, colon and mesenteric lymph nodes. An inverse correlation was found between Gag- and Env-specific central memory T cell responses on the day of challenge and plasma viremia at set point. Overall, the topical DermaVir/protein vaccination yields central memory T cell responses and facilitates control of pathogenic SHIV infection. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:197 / 211
页数:15
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