Department of Antigens and Sera Research, Veterinary Serum and Vaccine Research Institute, Agricultural Research Center, Egypt.
Nanotechnology and Advanced Material Central Lab, Agricultural Research Center, Giza, Egypt; Regional Center for Food and Feed, Agricultural Research Center, Giza, Egypt.
J Immunol Methods. 2022 Jul;506:113280. doi: 10.1016/j.jim.2022.113280. Epub 2022 May 13.
Nanovaccine is a revolutionary type of immunizations for various diseases that is simple to manufacture and administer. As a result, we are working to develop innovative nanovaccines against E. coli, which is capable of causing disease both inside and outside of its predilection sites, causing respiratory and systemic disease (colibacillosis).Colibacillosis is a global disease that significantly affects poultry production. The present study aims to evaluate in vivo cell-mediated immunity against a chitosan-nanovaccine from E. coli serogroups O1 and O78 to aid in limiting colibacillosis in chicken. Two hundred specific pathogen-free (SPF) three weeks old broiler chickens were used and divided into five groups: the first group inoculated with the outer membrane and flagellar antigen (OF), the second group inoculated with chitosan capsulated-outer membrane protein-flagellar antigen (CS-O-F), the third group inoculated with chitosan loaded-outer membrane protein-flagellar antigen (CS-O-F), the fourth group was vaccinated with (CS-O-F-M) adjuvanted with Montanide ISA 71 RVG, and the fifth group was left as unvaccinated control. The immune response was measured by ELISA, lymphocyte proliferation test, and challenge test. The duration of immunity was also studied. The CS-O-F-M had the highest antibody titer in an ELISA test using the O1 strain, and the CS-O-F had the highest antibody titer in an ELISA test using the O78 strain. For both O1 and O78 strains, the CS-O-F-M had the strongest cell-mediated immune response, which was validated by the challenge test and duration study. We recommend producing nanovaccines (CS-O-F-M) from E.coli O1 and O78 strains as a new manufacturing vaccine based on the demonstrated results. Because it produces highly effective humoral and cell-mediated immune responses, this novel vaccine may be useful in reducing the risk of colibacillosis.
纳米疫苗是一种针对各种疾病的革命性免疫制剂,其制造和使用都非常简便。因此,我们正在努力开发针对大肠杆菌的创新型纳米疫苗,这种疫苗能够在其偏好部位内外引发疾病,导致呼吸道和全身性疾病(大肠杆菌病)。大肠杆菌病是一种全球性疾病,对家禽生产有重大影响。本研究旨在评估壳聚糖纳米疫苗对大肠杆菌血清型 O1 和 O78 的体内细胞介导免疫反应,以帮助限制鸡大肠杆菌病。使用 200 只特定病原体无(SPF)三周龄肉鸡分为五组:第一组接种外膜和鞭毛抗原(OF),第二组接种壳聚糖包裹的外膜蛋白-鞭毛抗原(CS-O-F),第三组接种壳聚糖负载的外膜蛋白-鞭毛抗原(CS-O-F),第四组用蒙坦德 ISA 71 RVG 佐剂(CS-O-F-M)接种,第五组为未接种对照组。通过 ELISA、淋巴细胞增殖试验和攻毒试验来测量免疫反应。还研究了免疫持续时间。在使用 O1 株的 ELISA 试验中,CS-O-F-M 具有最高的抗体滴度,而在使用 O78 株的 ELISA 试验中,CS-O-F 具有最高的抗体滴度。对于 O1 和 O78 两种菌株,CS-O-F-M 具有最强的细胞介导免疫反应,攻毒试验和持续时间研究验证了这一点。鉴于已证明的结果,我们建议使用大肠杆菌 O1 和 O78 株生产纳米疫苗(CS-O-F-M)作为一种新型制造疫苗。由于这种新型疫苗可产生高效的体液和细胞介导免疫反应,因此可能有助于降低大肠杆菌病的风险。