Suppr超能文献

猪对传染性胃肠炎病毒结构蛋白的特异性细胞毒性淋巴细胞反应:一项使用淋巴母细胞系和重组痘苗病毒的研究

Specific cytotoxic lymphocyte response in swine against structural proteins of transmissible gastro-enteritis virus: a study using lymphoblastoid cell line and recombinant vaccinia virus.

作者信息

Murata H, Britton P, Kaeffer B, Aynaud J M, Chevaleyre C, Salmon H

机构信息

Laboratoire de pathologie infectieuse et immunologie, Nouzilly, France.

出版信息

Vet Res. 1998 Sep-Oct;29(5):467-74.

PMID:9779559
Abstract

To determine the specificity, if any, of cellular cytotoxicity against transmissible gastro-enteritis virus (TGEV) infected cells, we developed a test using B lymphoblasts from a MHC histocompatible (d/d haplotype) cell line (L14), as stimulating and target cells. These cells were previously infected with recombinant vaccinia virus including different TGEV structural genes, either the spike (vS), membrane (vM) or nucleoprotein gene (vN). Lymphocytes from a TGEV immunized (d/d) swine developed a cytotoxic activity after secondary in vitro stimulation in the presence of vS, vM or vN infected L14 cells. The cytotoxic activity was induced and directed against the homologous vS and vM infected cells but no cytotoxic activity occurred at all against vN infected cells. While vM infected cells induced a cytotoxic activity against vM infected cells only, vS infected cells stimulated a cross-reactive cytotoxic activity against vM and vN infected cells in addition to that against vS infected cells. This latter cytotoxicity may be due to an increase in a non-specific background of Natural Killer or lymphocyte activated killer activity, which is seen also after coculture with wild type vaccinia virus (vW) infected cells. Thus these results are of practical importance in two respects. First, lymphoïd B cell lines represent an excellent tool for determining which viral antigens are recognized by cytotoxic lymphocytes and second, they indicate the need to incorporate the M and S genes into a TGEV vaccine to induce cellular immunity against TGEV.

摘要

为了确定针对感染传染性胃肠炎病毒(TGEV)的细胞的细胞毒性(若有的话)的特异性,我们开发了一种检测方法,使用来自 MHC 组织相容性(d/d 单倍型)细胞系(L14)的 B 淋巴母细胞作为刺激细胞和靶细胞。这些细胞先前已感染包含不同 TGEV 结构基因的重组痘苗病毒,即刺突基因(vS)、膜基因(vM)或核蛋白基因(vN)。来自 TGEV 免疫的(d/d)猪的淋巴细胞在存在 vS、vM 或 vN 感染的 L14 细胞的情况下进行二次体外刺激后产生了细胞毒性活性。细胞毒性活性是针对同源的 vS 和 vM 感染细胞诱导产生的,但对 vN 感染细胞根本没有细胞毒性活性。虽然 vM 感染细胞仅诱导针对 vM 感染细胞的细胞毒性活性,但 vS 感染细胞除了针对 vS 感染细胞的细胞毒性活性外,还刺激了针对 vM 和 vN 感染细胞的交叉反应性细胞毒性活性。后一种细胞毒性可能是由于自然杀伤细胞或淋巴细胞激活杀伤活性的非特异性背景增加所致,这在与野生型痘苗病毒(vW)感染细胞共培养后也可见。因此,这些结果在两个方面具有实际重要性。首先,淋巴 B 细胞系是确定细胞毒性淋巴细胞识别哪些病毒抗原的优秀工具,其次,它们表明需要将 M 和 S 基因纳入 TGEV 疫苗以诱导针对 TGEV 的细胞免疫。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验