Mucosal adjuvants and delivery systems for protein-, DNA- and RNA-based vaccines

被引:80
作者
Vajdy, M [1 ]
Srivastava, I [1 ]
Polo, J [1 ]
Donnelly, J [1 ]
O'Hagan, D [1 ]
Singh, M [1 ]
机构
[1] Chiron Vaccines, Emeryville, CA 94608 USA
关键词
adjuvant; delivery system; immunomodulator; mucosal; vaccine;
D O I
10.1111/j.1440-1711.2004.01288.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Almost all vaccinations today are delivered through parenteral routes. Mucosal vaccination offers several benefits over parenteral routes of vaccination, including ease of administration, the possibility of self-administration, elimination of the chance of injection with infected needles, and induction of mucosal as well as systemic immunity. However, mucosal vaccines have to overcome several formidable barriers in the form of significant dilution and dispersion; competition with a myriad of various live replicating bacteria, viruses, inert food and dust particles; enzymatic degradation; and low pH before reaching the target immune cells. It has long been known that vaccination through mucosal membranes requires potent adjuvants to enhance immunogenicity, as well as delivery systems to decrease the rate of dilution and degradation and to target the vaccine to the site of immune function. This review is a summary of current approaches to mucosal vaccination, and it primarily focuses on adjuvants as immunopotentiators and vaccine delivery systems for mucosal vaccines based on protein, DNA or RNA. In this context, we define adjuvants as protein or oligonucleotides with immunopotentiating properties co-administered with pathogen-derived antigens, and vaccine delivery systems as chemical formulations that are more inert and have less immunomodulatory effects than adjuvants, and that protect and deliver the vaccine through the site of administration. Although vaccines can be quite diverse in their composition, including inactivated virus, virus-like particles and inactivated bacteria (which are inert), protein-like vaccines, and non-replicating viral vectors such as poxvirus and adenovirus (which can serve as DNA delivery systems), this review will focus primarily on recombinant protein antigens, plasmid DNA, and alphavirus-based replicon RNA vaccines and delivery systems. This review is not an exhaustive list of all available protein, DNA and RNA vaccines, with related adjuvants and delivery systems, but rather is an attempt to highlight many of the currently available approaches in immunopotentiation of mucosal vaccines.
引用
收藏
页码:617 / 627
页数:11
相关论文
共 152 条
[31]   Alphavirus replicon particles as candidate HIV vaccines [J].
Davis, NL ;
West, A ;
Reap, E ;
MacDonald, G ;
Collier, M ;
Dryga, S ;
Maughan, M ;
Connell, M ;
Walker, C ;
McGrath, K ;
Cecil, C ;
Ping, LH ;
Frelinger, J ;
Olmsted, R ;
Keith, P ;
Swanstrom, R ;
Williamson, C ;
Johnson, P ;
Montefiori, D ;
Johnston, RE .
IUBMB LIFE, 2002, 53 (4-5) :209-211
[32]   Safety and immunogenicity of MF59-adjuvanted influenza vaccine in the elderly [J].
De Donato, S ;
Granoff, D ;
Minutello, M ;
Lecchi, G ;
Faccini, M ;
Agnello, M ;
Senatore, F ;
Verweij, P ;
Fritzell, B ;
Podda, A .
VACCINE, 1999, 17 (23-24) :3094-3101
[33]   Plasmid DNA adsorbed onto cationic microparticles mediates target gene expression and antigen presentation by dendritic cells [J].
Denis-Mize, KS ;
Dupuis, M ;
MacKichan, ML ;
Singh, M ;
Doe, B ;
O'Hagan, D ;
Ulmer, JB ;
Donnelly, JJ ;
McDonald, DM ;
Ott, G .
GENE THERAPY, 2000, 7 (24) :2105-2112
[34]   PRECLINICAL EFFICACY OF A PROTOTYPE DNA VACCINE - ENHANCED PROTECTION AGAINST ANTIGENIC DRIFT IN INFLUENZA-VIRUS [J].
DONNELLY, JJ ;
FRIEDMAN, A ;
MARTINEZ, D ;
MONTGOMERY, DL ;
SHIVER, JW ;
MOTZEL, SL ;
ULMER, JB ;
LIU, MA .
NATURE MEDICINE, 1995, 1 (06) :583-587
[35]   DNA vaccines [J].
Donnelly, JJ ;
Ulmer, JB ;
Liu, MA .
LIFE SCIENCES, 1996, 60 (03) :163-172
[36]   Mucosal immunization with inactivated human immunodeficiency virus plus CpG oligodeoxynucleotides induces genital immune responses and protection against intravaginal challenge [J].
Dumais, N ;
Patrick, A ;
Moss, RB ;
Davis, HL ;
Rosenthal, KL .
JOURNAL OF INFECTIOUS DISEASES, 2002, 186 (08) :1098-1105
[37]   Dendritic cells internalize vaccine adjuvant after intramuscular injection [J].
Dupuis, M ;
Murphy, TJ ;
Higgins, D ;
Ugozzoli, M ;
van Nest, G ;
Ott, G ;
McDonald, DM .
CELLULAR IMMUNOLOGY, 1998, 186 (01) :18-27
[38]   Distribution of DNA vaccines determines their immunogenicity after intramuscular injection in mice [J].
Dupuis, M ;
Denis-Mize, K ;
Woo, C ;
Goldbeck, C ;
Selby, MJ ;
Chen, MC ;
Otten, GR ;
Ulmer, JB ;
Donnelly, JJ ;
Ott, G ;
McDonald, DM .
JOURNAL OF IMMUNOLOGY, 2000, 165 (05) :2850-2858
[39]  
EDELMAN R, 1997, NEW GENERATION VACCI, P173
[40]  
Egilmez NK, 2000, CANCER RES, V60, P3832