Department of Veterinary Pathology, Western College of Veterinary Medicine University of Saskatchewan, Saskatoon, Canada S7N 5B4.
Vaccinology and Immunotherapy, School of Public Health, University of Saskatchewan, Saskatoon, Canada 7N 5E3.
Avian Dis. 2024 Sep;68(3):240-253. doi: 10.1637/aviandiseases-D-24-00014.
(CP)-induced necrotic enteritis (NE) is an economically important disease in the broiler chicken industry. The incidence of NE is common in 3-to-6-wk-old broiler chickens, once maternal antibodies start declining. Developing an effective vaccination strategy against NE, preferably delivering a single dose of vaccine at hatch to protect broiler chickens against NE without a booster vaccine, is an enormous challenge. The objective of this study was to induce mucosal immunity in the intestines against NE by intrapulmonary (IPL) delivery of a live CP vaccine at hatch, exploiting the gut-lung-axis (GLA) concept by vaccine delivery following administration of cytosine-phosphorothioate-guanine oligodeoxynucleotides (CpG-ODN) to induce immune cell maturation in the lungs. Experiments were conducted to explore the dose of CP and immune protection against heterologous CP challenge, and to study the efficacy of IPL delivery of a CP vaccine without a booster. Additional studies were conducted to measure serum immunoglobulin (Ig)Y, mucosal IgA, and histopathology of lungs following vaccination. Delivery of a live CP vaccine by the IPL route, with or without CpG-ODN, provided significant protection against NE ( < 0.0001). Systemic IgY and mucosal IgA against CP were correlated with protection against NE. There was no necrosis or inflammation in the pulmonary parenchyma. There was a low number of CP isolated from the lungs following live CP delivery by the IPL route. A significant influx of ( < 0.001) of CD8+ T cells and macrophages were noted in the lungs 2 days following live CP delivery by the IPL route. IPL delivery of a live CP vaccine, rather than inactivated CP, provided better protection. This study demonstrated the utility in exploiting the GLA concept in vaccine delivery in broiler chickens.
(CP)诱导的坏死性肠炎(NE)是肉鸡产业中一种具有重要经济意义的疾病。NE 的发病率在 3 至 6 周龄的肉鸡中很常见,一旦母源抗体开始下降。开发针对 NE 的有效疫苗接种策略是一个巨大的挑战,最好在孵化时接种一剂疫苗,以在不使用加强疫苗的情况下保护肉鸡免受 NE 的侵害。本研究的目的是通过孵化时经肺内(IPL)接种活 CP 疫苗在肠道中诱导针对 NE 的黏膜免疫,通过接种胞嘧啶磷酸硫代鸟嘌呤寡脱氧核苷酸(CpG-ODN)以诱导肺部免疫细胞成熟来利用肠-肺轴(GLA)概念进行疫苗接种。进行了实验以探索 CP 的剂量和针对异源 CP 挑战的免疫保护,并研究了不使用加强疫苗接种 IPL 递送 CP 疫苗的功效。还进行了额外的研究来测量接种疫苗后的血清免疫球蛋白(Ig)Y、黏膜 IgA 和肺的组织病理学。通过 IPL 途径接种活 CP 疫苗,无论是否接种 CpG-ODN,都能显著预防 NE(<0.0001)。针对 CP 的系统 IgG 和黏膜 IgA 与预防 NE 呈正相关。肺实质中没有坏死或炎症。通过 IPL 途径接种活 CP 后,从肺部分离的 CP 数量很少。通过 IPL 途径接种活 CP 后,肺部观察到 CD8+T 细胞和巨噬细胞的大量涌入(<0.001)。通过 IPL 途径接种活 CP 疫苗而不是灭活 CP 疫苗提供了更好的保护。本研究证明了在肉鸡疫苗接种中利用 GLA 概念的实用性。