Poultry Diagnostic and Research Center, Department of Population Health, College of Veterinary Medicine, University of Georgia, 953 College Station Rd., Athens, GA 30602, USA.
Food Animal Health and Management Program, Department of Population Health, College of Veterinary Medicine, University of Georgia, 501 D. W. Brooks Dr., Athens, GA 30602, USA.
Viruses. 2019 Jul 10;11(7):635. doi: 10.3390/v11070635.
Infectious laryngotracheitis (ILT) is an acute respiratory disease of poultry caused by infectious laryngotracheitis virus (ILTV). Control of the disease with live attenuated vaccines administered via eye drop build upon immune responses generated by the eye-associated lymphoid tissues. The aim of this study was to assess cytokine and lymphocyte changes in the conjunctiva-associated lymphoid tissues (CALT) and Harderian gland (HG) stimulated by the ocular inoculation of the ILTV chicken embryo origin (CEO) vaccine strain and virulent strain 63140. This study offers strong evidence to support the roles that the CALT and HG play in the development of protective ILTV immune responses. It supports the premise that ILTV-mediated immunomodulation favors the B cell response over those of T cells. Further, it provides evidence that expansions of CD8α cells, with the concomitant expression of the gene, are key to reducing viral genomes in the CALT and halting ILTV cytolytic replication in the conjunctiva. Ultimately, this study revealed that the early upregulation of interleukin and Interferon ( cytokine genes, which shape the antigen-specific cell-mediated immune responses, retarded the decline of virus replication, and enhanced the development of lesions in the conjunctiva epithelium.
传染性喉气管炎(ILT)是一种由传染性喉气管炎病毒(ILTV)引起的家禽急性呼吸道疾病。通过滴眼途径用活减毒疫苗控制该疾病,依赖于由眼相关淋巴组织产生的免疫应答。本研究的目的是评估通过眼接种 ILTV 鸡胚源(CEO)疫苗株和强毒 63140 株刺激的结膜相关淋巴组织(CALT)和哈德腺(HG)中细胞因子和淋巴细胞的变化。本研究有力地证明了 CALT 和 HG 在保护性 ILTV 免疫应答的发展中所起的作用。它支持 ILTV 介导的免疫调节有利于 B 细胞应答而不是 T 细胞应答的前提。此外,它提供的证据表明,CD8α 细胞的扩增伴随着基因的表达,是减少 CALT 中病毒基因组并阻止传染性喉气管炎在结膜中的细胞溶解性复制的关键。最终,本研究表明,白细胞介素和干扰素(IFN)基因的早期上调,塑造了抗原特异性细胞介导的免疫应答,减缓了病毒复制的下降,并增强了结膜上皮病变的发展。