Enhancement of a human immunodeficiency virus env DNA vaccine using a novel polycationic nanoparticle formulation

被引:35
作者
Locher, CP
Putnam, D
Langer, R
Witt, SA
Ashlock, BM
Levy, JA
机构
[1] Univ Calif San Francisco, Dept Med, Div Hematol & Oncol, San Francisco, CA 94143 USA
[2] MIT, Dept Chem Engn, Cambridge, MA 02319 USA
关键词
adjuvant; antibodies; gene therapy; animal model; AIDS;
D O I
10.1016/j.imlet.2003.02.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In an effort to develop a more effective DNA immunization strategy for HIV, we synthesized an HIV-2 env DNA vaccine and delivered it in a novel polycationic adjuvant formulation that forms nanoparticles in solution and enhances protein expression. The polycationic adjuvant contained imidazole moieties to facilitate endosomal escape. Nanoparticles containing the DNA vaccine plasmid were formed by electrostatic condensation with the polycationic adjuvant. We hypothesized that this formulation would improve immune responses to the gp 140 env gene from HIV-2(UC2) by increasing the level of expressed antigen. We found that the nanoparticles were superior at inducing high levels of systemic antibody responses compared to naked DNA when delivered by the intradermal route in BALB/c mice. In addition, the nanoparticles induced higher levels of IgM, IgG, and IgA antibodies. These results suggest that nanoparticles may be an important adjuvant formulation to improve the effectiveness of genetic immunization and rationalize its use in the evaluation of vaccine candidates in non-human primate models for AIDS. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:67 / 70
页数:4
相关论文
共 13 条
[1]   Molecular cloning of the human immunodeficiency virus subtype 2 strain HIV-2(UC2) [J].
Barnett, SW ;
Legg, HS ;
Sun, Y ;
Klinger, J ;
Blackbourn, DJ ;
Locher, CP ;
Levy, JA .
VIROLOGY, 1996, 222 (01) :257-261
[2]  
FELGNER JH, 1994, J BIOL CHEM, V269, P2550
[3]   Vaccine entrapment in liposomes [J].
Gregoriadis, G ;
McCormack, B ;
Obrenovic, M ;
Saffie, R ;
Zadi, B ;
Perrie, Y .
METHODS-A COMPANION TO METHODS IN ENZYMOLOGY, 1999, 19 (01) :156-162
[4]   Nucleic acid immunization: concepts and techniques associated with third generation vaccines [J].
Hasan, UA ;
Abai, AM ;
Harper, DR ;
Wren, BW ;
Morrow, WJW .
JOURNAL OF IMMUNOLOGICAL METHODS, 1999, 229 (1-2) :1-22
[5]   Chitosan as a novel nasal delivery system for vaccines [J].
Illum, L ;
Jabbal-Gill, I ;
Hinchcliffe, M ;
Fisher, AN ;
Davis, SS .
ADVANCED DRUG DELIVERY REVIEWS, 2001, 51 (1-3) :81-96
[6]   Baboons as an animal model for human immunodeficiency virus pathogenesis and vaccine development [J].
Locher, CP ;
Witt, SA ;
Herndier, BG ;
Tenner-Racz, K ;
Racz, P ;
Levy, JA .
IMMUNOLOGICAL REVIEWS, 2001, 183 :127-140
[7]  
Mattner F, 2002, CANCER RES, V62, P1477
[8]   Key issues in non-viral gene delivery (Reprinted from Advanced Drug Delivery Reviews, vol 34, pg 3-19, 1998) [J].
Pouton, CW ;
Seymour, LW .
ADVANCED DRUG DELIVERY REVIEWS, 2001, 46 (1-3) :187-203
[9]   Polymer-based gene delivery with low cytotoxicity by a unique balance of side-chain termini [J].
Putnam, D ;
Gentry, CA ;
Pack, DW ;
Langer, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (03) :1200-+
[10]   New hope for an AIDS vaccine [J].
Robinson, HL .
NATURE REVIEWS IMMUNOLOGY, 2002, 2 (04) :239-250