TOWARDS VACCINE OPTIMIZATION

被引:20
作者
LUSSOW, AR
AGUADO, MT
DELGIUDICE, G
LAMBERT, PH
机构
[1] World Health Organisation-Immunology Research and Training Centre, Dept. of Pathology, University of Geneva, Geneva
关键词
Adjuvant; Carrier; Immunomodifier; Vaccine; Vector;
D O I
10.1016/0165-2478(90)90124-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
New molecular technologies have accelerated the search for sub-unit candidate vaccines. However, once identified the use of a candidate antigen must be optimised to reap the maximum benefit from the eventual vaccine. This optimisation should take into account both the needs of the target population, and the various ways of potentiating the protective immune response induced. One must be sure that the final product will be used. Hence, vaccine optimisation should strive toward meeting the needs of a specific epidemiological problem within the economic constraints of a given situation. This may be possible using novel delivery systems designed to limit the number of doses needed, improve the stability or facilitate the delivery of a particular vaccine. In meeting the needs of a target population in a field situation, one must also keep in mind certain safety factors that go beyond the usual regulatory constraints. The immune response to vaccine candidates can be potentiated in many ways. The ability to preferentially induce specific protective effector mechanisms: i.e., antibody isotypes, T-cell subsets, and T-cell sub-subsets, is becoming a reality. Carrier molecules designed to avoid the problems of epitope suppression and competition, and perhaps an eventual "carrier jam," are being developed. Adjuvants and immunostimulants may also help, but the critical issue here remains their acceptibility for use in man. Finally novel strategies for the induction of the immune response may also potentiate the immune response in the optimisation of vaccines. © 1990.
引用
收藏
页码:255 / 264
页数:10
相关论文
共 54 条
[1]  
ALLISON AC, 1983, NEW APPROACHES VACCI, P133
[2]  
ALTMAN A, 1989, ADV VET SCI COMP MED, V33, P301
[3]  
[Anonymous], 1988, LIPOSOMES DRUG CARRI
[5]  
BOMFORD R, 1980, CLIN EXP IMMUNOL, V39, P426
[6]   ADJUVANT FORMULATION FOR USE IN VACCINES TO ELICIT BOTH CELL-MEDIATED AND HUMORAL IMMUNITY [J].
BYARS, NE ;
ALLISON, AC .
VACCINE, 1987, 5 (03) :223-228
[7]   RELATIONSHIP OF STRUCTURE OF BACTERIAL LIPOPOLYSACCHARIDES TO ITS FUNCTION IN MITOGENESIS AND ADJUVANTICITY [J].
CHILLER, JM ;
SKIDMORE, BJ ;
MORRISON, DC ;
WEIGLE, WO .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1973, 70 (07) :2129-2133
[8]   COMPARISON OF CORYNEBACTERIUM-PARVUM AND BORDETELLA-PERTUSSIS WITH FREUNDS COMPLETE ADJUVANT AS IMMUNOPOTENTIATORS FOR BETA-HUMAN CHORIONIC-GONADOTROPIN LINKED TO AN ATOXIC FRAGMENT OF TETANUS TOXIN [J].
COVEY, DC ;
CHANG, CC ;
LAURENCE, KA .
AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 1989, 19 (01) :17-20
[9]  
DELGIUDICE G, 1989, SCAND J IMMUNOL, V29, P555, DOI 10.1111/j.1365-3083.1989.tb01158.x
[10]   INVIVO PRIMING OF VIRUS-SPECIFIC CYTO-TOXIC LYMPHOCYTES-T WITH SYNTHETIC LIPOPEPTIDE VACCINE [J].
DERES, K ;
SCHILD, H ;
WIESMULLER, KH ;
JUNG, G ;
RAMMENSEE, HG .
NATURE, 1989, 342 (6249) :561-564