Department of Pharmacy, University of Sargodha, Sargodha, Punjab, 40100 Pakistan.
Indian J Microbiol. 2008 Sep;48(3):401-4. doi: 10.1007/s12088-008-0048-8. Epub 2009 Mar 25.
The present study was conducted to develop and evaluate an experimental ISCOM-based infectious bursal disease (IBD) vaccine. The indigenous very virulent infectious bursal disease virus (vvIBDV) already attenuated and adapted to Vero cell line was used. After denaturation of viral proteins with sodium dodecyl sulphate (SDS), an IBD-ISCOM was constructed. The non-incorporated viral components were separated from ISCOM by centrifugation of dialysate. The pathogenicity and immunogenicity trials were conducted in 3-week-old broiler chicken. A commercial oil-emulsified vaccine (CEVAC IBD K) was used for comparison. There were no clinical signs of disease, gross or microscopic lesions in bursa of Fabricius in group G1 vaccinated with ISCOM-based vaccine and bursa to body weight ratio were comparable to un-vaccinated control group (G3). The virus-neutralizing antibody titers were significantly (P<0.05) higher in group G1 as compared with group G2 which was vaccinated with commercial vaccine. On challenge with vvIBDV, 100%, 75% and 0.00% protection was achieved in G1, G2 and G3, respectively. The results indicated that ISCOM-based IBD vaccine is safe and immunogenic.
本研究旨在开发和评估一种基于免疫刺激复合物(ISCOM)的传染性法氏囊病(IBD)疫苗。使用已减毒并适应 Vero 细胞系的本土高致病性传染性法氏囊病病毒(vvIBDV)。在十二烷基硫酸钠(SDS)变性病毒蛋白后,构建了 IBD-ISCOM。未结合的病毒成分通过透析液的离心从 ISCOM 中分离出来。在 3 周龄肉鸡中进行了致病性和免疫原性试验。使用商业油乳剂疫苗(CEVAC IBD K)进行比较。接种基于 ISCOM 的疫苗的 G1 组没有疾病临床症状、法氏囊的大体或显微镜病变,并且法氏囊与体重的比值与未接种对照组(G3)相当。与接种商业疫苗的 G2 组相比,G1 组的病毒中和抗体滴度显著(P<0.05)更高。在挑战 vvIBDV 时,G1、G2 和 G3 组的保护率分别为 100%、75%和 0.00%。结果表明,基于 ISCOM 的 IBD 疫苗是安全且具有免疫原性的。