Suppr超能文献

用 Ad5-85A 增强卡介苗(BCG)接种牛后获得的 Ag85A 特异性 CD4 T 细胞系具有抑制分枝杆菌生长和抗炎的特性。

Ag85A-specific CD4 T cell lines derived after boosting BCG-vaccinated cattle with Ad5-85A possess both mycobacterial growth inhibition and anti-inflammatory properties.

机构信息

TB Immunology and Vaccinology Team, Department of Bacteriology, Animal and Plant Health Agency, Weybridge, Surrey KT15 3NB, UK; Immunity Division, The Roslin Institute, Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush, Midlothian EH25 9RG, UK.

TB Immunology and Vaccinology Team, Department of Bacteriology, Animal and Plant Health Agency, Weybridge, Surrey KT15 3NB, UK.

出版信息

Vaccine. 2018 May 11;36(20):2850-2854. doi: 10.1016/j.vaccine.2018.03.068. Epub 2018 Apr 11.

Abstract

There is a need to improve the efficacy of the BCG vaccine against human and bovine tuberculosis. Previous data showed that boosting bacilli Calmette-Guerin (BCG)-vaccinated cattle with a recombinant attenuated human type 5 adenovirally vectored subunit vaccine (Ad5-85A) increased BCG protection and was associated with increased frequency of Ag85A-specific CD4 T cells post-boosting. Here, the capacity of Ag85A-specific CD4 T cell lines - derived before and after viral boosting - to interact with BCG-infected macrophages was evaluated. No difference before and after boosting was found in the capacity of these Ag85A-specific CD4 T cell lines to restrict mycobacterial growth, but the secretion of IL-10 in vitro post-boost increased significantly. Furthermore, cell lines derived post-boost had no statistically significant difference in the secretion of pro-inflammatory cytokines (IL-1β, IL-12, IFNγ or TNFα) compared to pre-boost lines. In conclusion, the protection associated with the increased number of Ag85A-specific CD4 T cells restricting mycobacterial growth may be associated with anti-inflammatory properties to limit immune-pathology.

摘要

需要提高卡介苗(BCG)疫苗对人类和牛型结核分枝杆菌的效力。先前的数据表明,用重组减毒人 5 型腺病毒载体亚单位疫苗(Ad5-85A)增强卡介苗接种牛的效力,可增加 BCG 的保护作用,并与增强后 Ag85A 特异性 CD4 T 细胞的频率增加有关。在此,评估了 Ag85A 特异性 CD4 T 细胞系 - 在病毒增强前后衍生的能力 - 与 BCG 感染的巨噬细胞相互作用。在增强前后,这些 Ag85A 特异性 CD4 T 细胞系限制分枝杆菌生长的能力没有差异,但增强后体外 IL-10 的分泌显著增加。此外,与增强前的细胞系相比,增强后衍生的细胞系在促炎细胞因子(IL-1β、IL-12、IFNγ或 TNFα)的分泌方面没有统计学上的显著差异。总之,与 Ag85A 特异性 CD4 T 细胞数量增加相关的保护作用可能与限制免疫病理学的抗炎特性有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09aa/5937909/d7bcbb13a07a/gr1.jpg

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