Adjuvants and delivery systems in veterinary vaccinology: current state and future developments

被引:99
作者
Heegaard, Peter M. H. [1 ]
Dedieu, Laurence [2 ]
Johnson, Nicholas [3 ]
Le Potier, Marie-Frederique [4 ]
Mockey, Michael [2 ]
Mutinelli, Franco [5 ]
Vahlenkamp, Thomas [6 ]
Vascellari, Marta [5 ]
Sorensen, Nanna Skall [1 ]
机构
[1] Tech Univ Denmark, Natl Vet Inst, Dept Vet Diagnost & Res, DK-1790 Copenhagen V, Denmark
[2] CIRAD, UMR CMAEE Controle Malad Anim, F-34398 Montpellier, France
[3] Vet Labs Agcy, Addlestone KT15 3NB, Surrey, England
[4] Anses Lab Ploufragan, Unite Virol & Immunol Porcines, F-22440 Les Croix, Ploufragan, France
[5] Ist Zooprofilatt Sperimentale Venezie, Dept Histopathol, I-35020 Legnaro, PD, Italy
[6] Fed Res Inst Anim Hlth, Friedrich Loeffler Inst, D-17493 Greifswald, Germany
关键词
TOLL-LIKE RECEPTORS; MYCOPLASMA-HYOPNEUMONIAE VACCINE; PLASMACYTOID DENDRITIC CELLS; RESPONSE MODIFIER IMIQUIMOD; PROTECTIVE IMMUNE-RESPONSES; MESSENGER-RNA EXPRESSION; PIG ALVEOLAR MACROPHAGES; BLOOD MONONUCLEAR-CELLS; TRANS-RETINOIC ACID; CPG-OLIGODEOXYNUCLEOTIDES;
D O I
10.1007/s00705-010-0863-1
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Modern adjuvants should induce strong and balanced immune responses, and it is often desirable to induce specific types of immunity. As an example, efficient Th1-immunity-inducing adjuvants are highly in demand. Such adjuvants promote good cell-mediated immunity against subunit vaccines that have low immunogenicity themselves. The development of such adjuvants may take advantage of the increased knowledge of the molecular mechanisms and factors controlling these responses. However, knowledge of such molecular details of immune mechanisms is relatively scarce for species other than humans and laboratory rodents, and in addition, there are special considerations pertaining to the use of adjuvants in veterinary animals, such as production and companion animals. With a focus on veterinary animals, this review highlights a number of approaches being pursued, including cytokines, CpG oligonucleotides, microparticles and liposomes.
引用
收藏
页码:183 / 202
页数:20
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