Overview of new vaccines and technologies

被引:6
作者
Chalmers, W. S. K. [1 ]
机构
[1] Intervet UK Ltd, Milton Keynes MK7 7AJ, Bucks, England
关键词
vaccines; technology; emerging diseases;
D O I
10.1016/j.vetmic.2006.04.006
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Molecular technology has given us a greater insight into the aetiology of disease, the functioning of the immune system and the mode of action of veterinary pathogens. The knowledge gained has been used to develop new vaccines with specific, reactive antigens which elicit protective immune mediated responses (humoral and/or cell mediated) in the host. These vaccines should not burden the immune system by initiating responses against non-essential antigens. However, the efficacy of these vaccines is only as good as the delivery technology or route used to present them to the immune system. Some vaccines, traditionally given by the parenteral route, are now given by the natural route; either orally or intranasally. Two major advantages, often interrelated, are the rapid onset of immunity and stimulation of the local, mucosal immunity. These new technologies are now making an impact on current vaccine development. The balance has to be found between what is technologically feasible and what will provide at least as good a protective immunity as current, conventional vaccines. As new and emerging diseases appear globally, new opportunities arise for molecular and conventional technologies to be applied to both the development and delivery of novel vaccines, as well as the improvement of vaccines in current use. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:25 / 31
页数:7
相关论文
共 29 条
[1]  
Bergman PJ, 2003, CLIN CANCER RES, V9, P1284
[2]   Prevalence and risk factors for feline Bordetella bronchiseptica infection [J].
Binns, SH ;
Dawson, S ;
Speakman, AJ ;
Cuevas, LE ;
Gaskell, CJ ;
Hart, CA ;
Morgan, KL ;
Gaskell, RM .
VETERINARY RECORD, 1999, 144 (21) :575-580
[3]   Serological evidence of West Nile virus, Usutu virus and Sindbis virus infection of birds in the UK [J].
Buckley, A ;
Dawson, A ;
Moss, SR ;
Hinsley, SA ;
Bellamy, PE ;
Gould, EA .
JOURNAL OF GENERAL VIROLOGY, 2003, 84 :2807-2817
[4]  
CAREY S, 2004, DVM NEWSMAGAZIN 0601
[5]   A COMPARISON OF CANINE-DISTEMPER VACCINE AND MEASLES-VACCINE FOR THE PREVENTION OF CANINE-DISTEMPER IN YOUNG PUPPIES [J].
CHALMERS, WSK ;
BAXENDALE, W .
VETERINARY RECORD, 1994, 135 (15) :349-353
[6]   PRELIMINARY DEVELOPMENT OF A LIVE ATTENUATED CANINE PARVOVIRUS VACCINE FROM AN ISOLITE OF BRITISH ORIGIN [J].
CHURCHILL, AE .
VETERINARY RECORD, 1987, 120 (14) :334-339
[7]   Modified vaccinia virus Ankara as antigen delivery system: how can we best use its potential? [J].
Drexler, I ;
Staib, C ;
Sutter, G .
CURRENT OPINION IN BIOTECHNOLOGY, 2004, 15 (06) :506-512
[8]  
Gaskell RM, 2002, VET REC, V150, P126
[9]   COMPARISON OF ISOLATES OF CANINE PARVOVIRUS BY RESTRICTION ENZYME ANALYSIS, AND VACCINE EFFICACY AGAINST FIELD STRAINS [J].
GREENWOOD, NM ;
CHALMERS, WSK ;
BAXENDALE, W ;
THOMPSON, H .
VETERINARY RECORD, 1995, 136 (03) :63-67
[10]   Development of a single dose tetanus toxoid formulation based on polymeric microspheres: a comparative study of poly(D,L-lactic-co-glycolic acid) versus chitosan microspheres [J].
Jaganathan, KS ;
Rao, YUB ;
Singh, P ;
Prabakaran, D ;
Gupta, S ;
Jain, A ;
Vyas, SP .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2005, 294 (1-2) :23-32