ORAL DELIVERY OF VACCINES - FORMULATION AND CLINICAL PHARMACOKINETIC CONSIDERATIONS

被引:47
作者
OHAGAN, DT
机构
[1] Department of Pharmaceutical Sciences, University of Nottingham, Nottingham, NG7 2RD, University Park
关键词
D O I
10.2165/00003088-199222010-00001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In recent years, there has been a gradual acceptance of the important role of sIgA in protecting mucosal surfaces against infection with a wide range of pathogenic organisms. Since sIgA is most efficiently stimulated by local application of antigens, there has been an increasing emphasis on the role of oral immunisation. The numerous advantages of the oral route over alternative routes of administration has driven the search for effective vaccines, often despite disappointing results. Nevertheless, recent developments in recombinant DNA technology and in the formulation of antigen delivery systems have given rise to justified optimism that the next decade will see the development of several new and improved oral vaccines (table IV). These vaccines will undoubtedly come to play an important role in preventing diseases caused by a number of pathogenic organisms which are currently poorly controlled. New oral vaccines are likely to be particularly beneficial in the Third World, where intestinal infections still cause a massive toll of preventable deaths. Because of the existence of the common mucosal immune system, new oral vaccines also offer the promise of control over several sexually transmitted diseases for which there are no vaccines currently available. © 1992, Adis International Limited. All rights reserved.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 46 条
[1]  
AMBRUSTER C, 1990, J INFECT DIS, V162, P1216
[2]  
BERGMANN KC, 1988, REV INFECT DIS, V10, P939
[3]  
Besredka A., 1927, LOCAL IMMUNIZATION
[4]   HIV IMMUNIZATION - FRESH PATHWAYS TO FOLLOW [J].
BOLOGNESI, DP .
NATURE, 1990, 344 (6269) :818-819
[5]   USE OF A VACCINIA RABIES RECOMBINANT VIRUS FOR THE ORAL VACCINATION OF FOXES AGAINST RABIES [J].
BROCHIER, B ;
THOMAS, I ;
BAUDUIN, B ;
LEVEAU, T ;
PASTORET, PP ;
LANGUET, B ;
CHAPPUIS, G ;
DESMETTRE, P ;
BLANCOU, J ;
ARTOIS, M .
VACCINE, 1990, 8 (02) :101-104
[6]   ANTIGEN CHIMERAS OF POLIOVIRUS AS POTENTIAL NEW VACCINES [J].
BURKE, KL ;
DUNN, G ;
FERGUSON, M ;
MINOR, PD ;
ALMOND, JW .
NATURE, 1988, 332 (6159) :81-82
[7]  
CHALLACOMBE SJ, 1991, IN PRESS IMMUNOLOGY
[8]   LIVE SALMONELLA AS VACCINES AND CARRIERS OF FOREIGN ANTIGENIC DETERMINANTS [J].
CHATFIELD, SN ;
STRUGNELL, RA ;
DOUGAN, G .
VACCINE, 1989, 7 (06) :495-498
[9]   ADJUVANT EFFECTS OF ORALLY-ADMINISTERED SAPONINS ON HUMORAL AND CELLULAR IMMUNE-RESPONSES IN MICE [J].
CHAVALI, SR ;
CAMPBELL, JB .
IMMUNOBIOLOGY, 1987, 174 (03) :347-359
[10]   EVALUATION OF ADENOVIRUS TYPE-4 AND TYPE-7 RECOMBINANT HEPATITIS-B VACCINES IN DOGS [J].
CHENGALVALA, M ;
LUBECK, MD ;
DAVIS, AR ;
MIZUTANI, S ;
MOLNARKIMBER, K ;
MORIN, J ;
HUNG, PP .
VACCINE, 1991, 9 (07) :485-490