Progress and Challenges toward the Development of Vaccines against Avian Infectious Bronchitis

被引:112
作者
Bande, Faruku [1 ,2 ]
Arshad, Siti Suri [1 ]
Bejo, Mohd Hair [1 ,3 ]
Moeini, Hassan [4 ]
Omar, Abdul Rahman [1 ,3 ]
机构
[1] Univ Putra Malaysia, Fac Vet Med, Dept Vet Pathol & Microbiol, Serdang 43400, Selangor, Malaysia
[2] Minist Anim Hlth & Fisheries Dev, Dept Vet Serv, Sokoto 840221, Sokoto State, Nigeria
[3] Univ Putra Malaysia, Inst Biosci, Lab Vaccine & Immunotherapeut, Serdang 43400, Selangor, Malaysia
[4] German Canc Res Ctr, Dept Virus Associated Tumours F100, D-69120 Heidelberg, Germany
关键词
CORONAVIRUS-M-PROTEIN; PROTECTIVE IMMUNE-RESPONSE; CYTOTOXIC T-LYMPHOCYTES; VIRUS-LIKE PARTICLES; SPIKE PROTEIN; S1; GLYCOPROTEIN; DNA VACCINE; N-PROTEIN; NUCLEOCAPSID PROTEIN; LACTOCOCCUS-LACTIS;
D O I
10.1155/2015/424860
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Avian infectious bronchitis (IB) is a widely distributed poultry disease that has huge economic impact on poultry industry. The continuous emergence of new IBV genotypes and lack of cross protection among different IBV genotypes have been an important challenge. Although live attenuated IB vaccines remarkably induce potent immune response, the potential risk of reversion to virulence, neutralization by the maternal antibodies, and recombination and mutation events are important concern on their usage. On the other hand, inactivated vaccines induce a weaker immune response and may require multiple dosing and/or the use of adjuvants that probably have potential safety risks and increased economic burdens. Consequently, alternative IB vaccines are widely sought. Recent advances in recombinant DNA technology have resulted in experimental IB vaccines that show promise in antibody and T-cells responses, comparable to live attenuated vaccines. Recombinant DNA vaccines have also been enhanced to target multiple serotypes and their efficacy has been improved using delivery vectors, nanoadjuvants, and in ovo vaccination approaches. Although most recombinant IB DNA vaccines are yet to be licensed, it is expected that these types of vaccines may hold sway as future vaccines for inducing a cross protection against multiple IBV serotypes.
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页数:12
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