Polynucleotide vaccines: potential for inducing immunity in animals

被引:8
作者
Babiuk, LA
Lewis, J
Suradhat, S
Baca-Estrada, M
Foldvari, M
Babiuk, S
机构
[1] VIDO, Saskatoon, SK S7N 5E3, Canada
[2] Univ Saskatchewan, Coll Pharm & Nutr, Saskatoon, SK, Canada
关键词
polynucleotide vaccines; immunization; animals;
D O I
10.1016/S0168-1656(99)00116-9
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Polynucleotide immunization has been described as the Third Revolution in Vaccinology. Early studies suggest the potential benefits of this form of immunization including: long-lived immunity, a broad-spectrum of immune responses (both cell mediated immunity, and humoral responses) and the simultaneous induction of immunity to a variety of pathogens through the use of multivalent vaccines. Using a murine model, we studied methods to enhance and direct the immune response to polynucleotide vaccines. We demonstrated the ability to modulate the magnitude and direction of the immune response by co-administration of plasmid encoded cytokines and antigen. Also, we clearly demonstrated that the cellular components (cytosolic, membrane-anchored, or extracellular) to which the expressed antigen is delivered determines the types of immune responses induced. Since induction of immunity at mucosal surfaces (route of entry for many pathogens) is critical to prevent infection, various methods of delivering polynucleotide vaccines to mucosal surfaces have been attempted and are described. Expansion of studies in various species, using natural models, should be extremely helpful in demonstrating the universality of this approach to immunization and more importantly, accurately identify parameters that are critical for the development of protective immunity. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:131 / 140
页数:10
相关论文
共 61 条
[21]   Induction of mucosal immunity against herpes simplex virus by plasmid DNA immunization [J].
Kuklin, N ;
Daheshia, M ;
Karem, K ;
Manickan, E ;
Rouse, BT .
JOURNAL OF VIROLOGY, 1997, 71 (04) :3138-3145
[22]   DELIVERY OF PLASMID DNA INTO MAMMALIAN-CELL LINES USING PH-SENSITIVE LIPOSOMES - COMPARISON WITH CATIONIC LIPOSOMES [J].
LEGENDRE, JY ;
SZOKA, FC .
PHARMACEUTICAL RESEARCH, 1992, 9 (10) :1235-1242
[23]   MUCOSAL MODEL OF GENITAL IMMUNIZATION IN MALE RHESUS MACAQUES WITH A RECOMBINANT SIMIAN IMMUNODEFICIENCY VIRUS P27 ANTIGEN [J].
LEHNER, T ;
TAO, L ;
PANAGIOTIDI, C ;
KLAVINSKIS, LS ;
BROOKES, R ;
HUSSAIN, L ;
MEYERS, N ;
ADAMS, SE ;
GEARING, AJH ;
BERGMEIER, LA .
JOURNAL OF VIROLOGY, 1994, 68 (03) :1624-1632
[24]   Polynucleotide vaccines in animals: Enhancing and modulating responses [J].
Lewis, PJ ;
Cox, GJM ;
LittelvandenHurk, SV ;
Babiuk, LA .
VACCINE, 1997, 15 (08) :861-864
[25]   New cationic lipid formulations for gene transfer [J].
Liu, F ;
Yang, JP ;
Huang, L ;
Liu, DX .
PHARMACEUTICAL RESEARCH, 1996, 13 (12) :1856-1860
[26]  
LUE C, 1994, CLIN EXP IMMUNOL, V96, P356
[27]   DNA vaccination with cytokine fusion constructs biases the immune response to ovalbumin [J].
Maecker, HT ;
Umetsu, DT ;
DeKruyff, RH ;
Levy, S .
VACCINE, 1997, 15 (15) :1687-1696
[28]   Enhancement of immune response to naked DNA vaccine by immunization with transfected dendritic cells [J].
Manickan, E ;
Kanangat, S ;
Rouse, RJD ;
Yu, ZY ;
Rouse, BT .
JOURNAL OF LEUKOCYTE BIOLOGY, 1997, 61 (02) :125-132
[29]  
Mocci S, 1997, J IMMUNOL, V158, P1559
[30]   Polyvinyl derivatives as novel interactive polymers for controlled gene delivery to muscle [J].
Mumper, RJ ;
Duguid, JG ;
Anwer, K ;
Barron, MK ;
Nitta, H ;
Rolland, AP .
PHARMACEUTICAL RESEARCH, 1996, 13 (05) :701-709