Adjuvants for vaccines, a quest

被引:30
作者
Audibert, F
机构
关键词
adjuvants; vaccines; moiety;
D O I
10.1016/S1567-5769(03)00011-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Efficient vaccines comprise a specific moiety: the structures presenting the protective antgenic determinants, and a nonspecific moiety: the adjuvant components. Dramatic advances have been reported concerning the specific moiety and new and highly purified immunogens have been defined and prepared. The use of vaccines is no longer restricted to the prevention of infections, they are now considered as therapeutic tools especially in cancer immunotherapy. In contrast, alum is still the only adjuvant suitable for clinical application. The success of the new avenues opened in vaccinology depends on the availability of appropriate immunomodulating preparations. For each given type of vaccine, the optimal profile of activity of the adjuvant moiety has to be defined, according to the response required to provide protection or cure. Thus, it is urgent to design and develop adjuvants active not only on the humoral responses but also on the cellular immune responses. This adjuvant function must have the capacity of turning on the innate responses, which play a decisive and instructive role in emanating the adaptive immune responses. These considerations encourage one to finalize immunomodulating procedures rather than to look only for new adjuvant compounds. Manipulations of dendritic cells (DCs), use of heat-shock proteins (HSPs) as carriers endowed of adjuvant activity or introduction of varying immunostimulating motives in genetic vaccines represent examples illustrating this new rationale. (C) 2003 Published by Elsevier Science B.V.
引用
收藏
页码:1187 / 1193
页数:7
相关论文
共 58 条
[1]   Dendritic cells acquire antigen from apoptotic cells and induce class I restricted CTLs [J].
Albert, ML ;
Sauter, B ;
Bhardwaj, N .
NATURE, 1998, 392 (6671) :86-89
[2]   CROSS-PRIMING OF MINOR HISTOCOMPATIBILITY ANTIGEN-SPECIFIC CYTOTOXIC T-CELLS UPON IMMUNIZATION WITH THE HEAT-SHOCK PROTEIN GP96 [J].
ARNOLD, D ;
FAATH, S ;
RAMMENSEE, HG ;
SCHILD, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (03) :885-889
[3]  
Asea A, 2000, CELL STRESS CHAPERON, V5, P425, DOI 10.1379/1466-1268(2000)005<0425:HPBAPN>2.0.CO
[4]  
2
[5]   Human TLR9 confers responsiveness to bacterial DNA via species-specific CpG motif recognition [J].
Bauer, S ;
Kirschning, CJ ;
Häcker, H ;
Redecke, V ;
Hausmann, S ;
Akira, S ;
Wagner, H ;
Lipford, GB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (16) :9237-9242
[6]   Cytokines as a link between innate and adaptive antitumor immunity [J].
Belardelli, F ;
Ferrantini, M .
TRENDS IN IMMUNOLOGY, 2002, 23 (04) :201-208
[7]   Relevance of the tumor antigen in the validation of three vaccination strategies for melanoma [J].
Bellone, M ;
Cantarella, D ;
Castiglioni, P ;
Crosti, MC ;
Ronchetti, A ;
Moro, M ;
Garancini, MP ;
Casorati, G ;
Dellabona, P .
JOURNAL OF IMMUNOLOGY, 2000, 165 (05) :2651-2656
[8]   CD91: a receptor for heat shock protein gp96 [J].
Binder, RJ ;
Han, DK ;
Srivastava, PK .
NATURE IMMUNOLOGY, 2000, 1 (02) :151-155
[9]   Heat shock protein-peptide complexes, reconstituted in vitro, elicit peptide-specific cytotoxic T lymphocyte response and tumor immunity [J].
Blachere, NE ;
Li, ZH ;
Chandawarkar, RY ;
Suto, R ;
Jaikaria, NS ;
Basu, S ;
Udono, H ;
Srivastava, PK .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (08) :1315-1322
[10]  
BOON T, 1994, ANNU REV IMMUNOL, V12, P337, DOI 10.1146/annurev.iy.12.040194.002005