Adjuvants for porcine reproductive and respiratory syndrome virus vaccines

被引:37
作者
Charerntantanakul, Wasin [1 ]
机构
[1] Maejo Univ, Dept Biol, Fac Sci, Chiang Mai 50290, Thailand
关键词
Vaccine adjuvant; Porcine reproductive and respiratory syndrome virus; Cell-mediated immune response; Antibody; MESSENGER-RNA EXPRESSION; HUMAN RECOMBINANT INTERLEUKIN-2; INTERFERON-GAMMA RESPONSE; MUCOSAL IMMUNE-RESPONSES; BLOOD MONONUCLEAR-CELLS; MOUTH-DISEASE VIRUS; TOLL-LIKE RECEPTOR; COLI ORAL VACCINE; INFECTED IN-UTERO; NATURAL-KILLER;
D O I
10.1016/j.vetimm.2008.12.018
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
This review deals with present and past efforts in utilization of vaccine adjuvants for porcine reproductive and respiratory syndrome virus (PRRSV) vaccines. PRRSV vaccines elicit delayed and weak cell-mediated immune (CMI) and antibody responses after vaccination. Several kinds of vaccine adjuvants have been utilized to accelerate and magnify immune responses to PRRSV vaccines. These adjuvants include cytokines, chemical reagents, and bacterial products. Of 11 vaccine adjuvants tested, five (i.e. interleukin-2 (IL-2), IL-12, interferon alpha (IFN alpha), polyinosinic and polycytidylic acid, and cytidine-phosphate-guanosine oligodeoxynucleotides (CpG ODN)) significantly enhance CMI response to PRRSV vaccines. The response is characterized by proliferation, cytotoxicity, and IFN gamma secretion of peripheral blood mononuclear cells or T cells in response to recall PRRSV antigens in vitro. Two (i.e. CpG ODN and cholera toxin) significantly enhance PRRSV-specific antibody response after vaccination. Two (i.e. IL-2 and CpG ODN) significantly enhance protective efficacy of PRRSV vaccines in challenge models. Improvement of immune responses to PRRSV vaccines should focus in future studies on assessing more vaccine adjuvants for their efficiency in enhancing both CMI and antibody responses and on identifying PRRSV components and strategies that down-modulate pig immune responses in order to devise vaccine adjuvants that can regulate such strategies of the virus. (c) 2008 Elsevier B.V. All rights reserved.
引用
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页码:1 / 13
页数:13
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