Live porcine reproductive and respiratory syndrome virus vaccines: Current status and future direction

被引:153
作者
Renukaradhya, Gourapura J. [1 ]
Meng, Xiang-Jin [2 ]
Calvert, Jay G. [3 ]
Roof, Michael [4 ]
Lager, Kelly M. [5 ]
机构
[1] Ohio State Univ, Ohio Agr Res & Dev Ctr, Dept Vet Prevent Med, Food Anim Hlth Res Program, Wooster, OH 44691 USA
[2] Virginia Polytech Inst & State Univ, Coll Vet Med, Dept Biomed Sci & Pathobiol, Blacksburg, VA 24061 USA
[3] Zoetis, Kalamazoo, MI USA
[4] Boehringer Ingelheim Vetmedica Inc, Ames, IA USA
[5] USDA, Virus & Prion Res Unit, Natl Anim Dis Ctr, Ames, IA USA
关键词
Porcine reproductive and respiratory syndrome virus (PRRSV); PRRSV-MLV; Immunity; Cross-protection; Vectors; Infectious cDNA clones; FULL-LENGTH CDNA; NUCLEAR-LOCALIZATION SIGNAL; RECOMBINANT PSEUDORABIES VIRUS; NONSTRUCTURAL PROTEIN-2 NSP2; GREEN FLUORESCENT PROTEIN; SMALL ENVELOPE PROTEIN; AMINO-ACID-RESIDUES; INFECTIOUS CLONE; NUCLEOCAPSID PROTEIN; IN-VITRO;
D O I
10.1016/j.vaccine.2015.06.092
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Porcine reproductive and respiratory syndrome (PRRS) caused by PRRS virus (PRRSV) was reported in the late 1980s. PRRS still is a huge economic concern to the global pig industry with a current annual loss estimated at one billion US dollars in North America alone. It has been 20 years since the first modified live-attenuated PRRSV vaccine (PRRSV-MLV) became commercially available. PRRSV-MLVs provide homologous protection and help in reducing shedding of heterologous viruses, but they do not completely protect pigs against heterologous field strains. There have been many advances in understanding the biology and ecology of PRRSV; however, the complexities of virus-host interaction and PRRSV vaccinology are not yet completely understood leaving a significant gap for improving breadth of immunity against diverse PRRS isolates. This review provides insights on immunization efforts using infectious PRRSV-based vaccines since the 1990s, beginning with live PRRSV immunization, development and commercialization of PRRSV-MLV, and strategies to overcome the deficiencies of PRRSV-MLV through use of replicating viral vectors expressing multiple PRRSV membrane proteins. Finally, powerful reverse genetics systems (infectious cDNA clones) generated from more than 20 PRRSV isolates of both genotypes I and 2 viruses have provided a great resource for exploring many innovative strategies to improve the safety and cross-protective efficacy of live PRRSV vaccines. Examples include vaccines with diminished ability to down-regulate the immune system, positive and negative marker vaccines, multivalent vaccines incorporating antigens from other porcine pathogens, vaccines that carry their own cytokine adjuvants, and chimeric vaccine viruses with the potential for broad cross-protection against heterologous strains. To combat this devastating pig disease in the future, evaluation and commercialization of such improved live PRRSV vaccines is a shared goal among PRRSV researchers, pork producers and biologics companies. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4069 / 4080
页数:12
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