Native-like, long synthetic peptides as components of sub-unit vaccines: practical and theoretical considerations for their use in humans

被引:14
作者
Demotz, S
Moulon, C
Roggero, MA
Fasel, N
Masina, S
机构
[1] DICTAGENE, CH-1066 Epalinges, Switzerland
[2] Univ Lausanne, Inst Biochem, CH-1066 Epalinges, Switzerland
关键词
bonds; disulfide; folding; peptides; synthetic; vaccine;
D O I
10.1016/S0161-5890(01)00077-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vaccines have been used as a successful tool in medicine by way of controlling many major diseases. In spite of this, vaccines today represent only a handful of all infectious diseases. Therefore, there is a pressing demand for improvements of existing vaccines with particular reference to higher efficacy and undisputed safety profiles. To this effect, as an alternative to available vaccine technologies, there has been a drive to develop vaccine candidate polypeptides by chemical synthesis. In our laboratory, we have recently developed a technology to manufacture long synthetic peptides of up to 130 residues, which are correctly folded and biologically active. This paper discusses the advantages of the molecularly defined, long synthetic peptide approach in the context of vaccine design, development and use in human vaccination. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:415 / 422
页数:8
相关论文
共 56 条
[11]  
De Palma R, 2000, ALLERGY, V55, P56
[12]   Why do we lack an effective vaccine against herpes simplex virus infections? [J].
Deshpande, SP ;
Kumaraguru, U ;
Rouse, BT .
MICROBES AND INFECTION, 2000, 2 (08) :973-978
[13]   Heteroclitic immunization induces tumor immunity [J].
Dyall, R ;
Bowne, WB ;
Weber, LW ;
LeMaoult, J ;
Szabo, P ;
Moroi, Y ;
Piskun, G ;
Lewis, JJ ;
Houghton, AN ;
Nikolic-Zugic, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (09) :1553-1561
[14]   New strategies for closing the gap of measles susceptibility in infants: towards vaccines compatible with current vaccination schedules [J].
El Kasmi, KC ;
Muller, CP .
VACCINE, 2001, 19 (17-19) :2238-2244
[15]   PRODUCTION AND IMMUNOLOGICAL ANALYSIS OF RECOMBINANT HEPATITIS-B VACCINE [J].
EMINI, EA ;
ELLIS, RW ;
MILLER, WJ ;
MCALEER, WJ ;
SCOLNICK, EM ;
GERETY, RJ .
JOURNAL OF INFECTION, 1986, 13 :3-&
[16]   Maternal immunization against viral disease [J].
Englund, J ;
Glezen, WP ;
Piedra, PA .
VACCINE, 1998, 16 (14-15) :1456-1463
[17]  
Fooks AR, 2000, CURR OPIN MOL THER, V2, P80
[18]   Mutant hepatitis B viruses:: a matter of academic interest only or a problem with far-reaching implications? [J].
François, G ;
Kew, M ;
Van Damme, P ;
Mphahlele, MJ ;
Meheus, A .
VACCINE, 2001, 19 (28-29) :3799-3815
[19]   Oral tolerance [J].
Garside, P ;
Mowat, AM .
SEMINARS IN IMMUNOLOGY, 2001, 13 (03) :177-185
[20]   Safety and immunogenicity of intranasally administered inactivated trivalent virosome-formulated influenza vaccine containing Escherichia coli heat-labile toxin as a mucosal adjuvant [J].
Glück, R ;
Mischler, R ;
Durrer, P ;
Fürer, E ;
Lang, AB ;
Herzog, C ;
Cryz, SJ .
JOURNAL OF INFECTIOUS DISEASES, 2000, 181 (03) :1129-1132