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新型强效 IFN-γ 诱导 CD8 T 细胞表位在不同牛病毒性腹泻病毒株中保守。

Novel Potent IFN-γ-Inducing CD8 T Cell Epitopes Conserved among Diverse Bovine Viral Diarrhea Virus Strains.

机构信息

Department of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, KS 66506; and

Department of Veterinary Pathobiology, Texas A&M University, College Station, TX 77843.

出版信息

J Immunol. 2021 Apr 15;206(8):1709-1718. doi: 10.4049/jimmunol.2001424. Epub 2021 Mar 24.

Abstract

Studies of immune responses elicited by bovine viral diarrhea virus (BVDV) vaccines have primarily focused on the characterization of neutralizing B cell and CD4 T cell epitopes. Despite the availability of commercial vaccines for decades, BVDV prevalence in cattle has remained largely unaffected. There is limited knowledge regarding the role of BVDV-specific CD8 T cells in immune protection, and indirect evidence suggests that they play a crucial role during BVDV infection. In this study, the presence of BVDV-specific CD8 T cells that are highly cross-reactive in cattle was demonstrated. Most importantly, novel potent IFN-γ-inducing CD8 T cell epitopes were identified from different regions of BVDV polyprotein. Eight CD8 T cell epitopes were identified from the following structural BVDV Ags: E, E1, and E2 glycoproteins. In addition, from nonstructural BVDV Ags N, NS2-3, NS4A-B, and NS5A-B, 20 CD8 T cell epitopes were identified. The majority of these IFN-γ-inducing CD8 T cell epitopes were found to be highly conserved among more than 200 strains from BVDV-1 and -2 genotypes. These conserved epitopes were also validated as cross-reactive because they induced high recall IFN-γCD8 T cell responses ex vivo in purified bovine CD8 T cells isolated from BVDV-1- and -2-immunized cattle. Altogether, 28 bovine MHC class I-binding epitopes were identified from key BVDV Ags that can elicit broadly reactive CD8 T cells against diverse BVDV strains. The data presented in this study will lay the groundwork for the development of a contemporary CD8 T cell-based BVDV vaccine capable of addressing BVDV heterogeneity more effectively than current vaccines.

摘要

对牛病毒性腹泻病毒 (BVDV) 疫苗引起的免疫反应的研究主要集中在中和 B 细胞和 CD4 T 细胞表位的特征描述上。尽管几十年来已有商业化疫苗,但牛的 BVDV 流行率仍基本未受影响。对于 BVDV 特异性 CD8 T 细胞在免疫保护中的作用知之甚少,间接证据表明它们在 BVDV 感染过程中发挥着至关重要的作用。本研究证明了牛体内存在高度交叉反应的 BVDV 特异性 CD8 T 细胞。最重要的是,从 BVDV 多蛋白的不同区域鉴定出了新型有效的 IFN-γ诱导性 CD8 T 细胞表位。从 BVDV 结构抗原 E、E1 和 E2 糖蛋白中鉴定出 8 个 CD8 T 细胞表位。此外,从非结构 BVDV 抗原 N、NS2-3、NS4A-B 和 NS5A-B 中鉴定出 20 个 CD8 T 细胞表位。这些 IFN-γ诱导性 CD8 T 细胞表位中的大多数在来自 BVDV-1 和 -2 基因型的 200 多个毒株中高度保守。这些保守的表位也被验证为具有交叉反应性,因为它们在从 BVDV-1 和 -2 免疫牛中分离的纯化牛 CD8 T 细胞中体外诱导了高召回 IFN-γCD8 T 细胞反应。总共从关键的 BVDV 抗原中鉴定出了 28 个牛 MHC Ⅰ类结合表位,这些表位可以引发针对多种 BVDV 株的广泛反应性 CD8 T 细胞。本研究中提供的数据为开发一种基于当代 CD8 T 细胞的 BVDV 疫苗奠定了基础,这种疫苗比现有疫苗更有效地解决 BVDV 异质性问题。

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