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牛 γδ T 细胞在皮下接种卡介苗后存在先天训练的证据。

Evidence of innate training in bovine γδ T cells following subcutaneous BCG administration.

机构信息

Department of Veterinary Microbiology and Preventive Medicine, Iowa State University, Ames, IA, United States.

Immunology, Cargill Animal Nutrition & Health, Elk River, MN, United States.

出版信息

Front Immunol. 2024 Jul 18;15:1423843. doi: 10.3389/fimmu.2024.1423843. eCollection 2024.

DOI:10.3389/fimmu.2024.1423843
PMID:39100669
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11295143/
Abstract

The Bacillus Calmette Guerin (BCG) vaccine has been shown to induce non-specific protection against diseases other than tuberculosis in vaccinated individuals, attributed to the induction of trained immunity. We have previously demonstrated that BCG administration induces innate immune training in mixed peripheral blood mononuclear cells and monocytes in calves. Gamma Delta (γδ) T cells are non-conventional T cells that exhibit innate and adaptive immune system features. They are in higher proportion in the peripheral blood of cattle than humans or rodents and play an essential role in bovine immune response to pathogens. In the current study, we determined if BCG administration induced innate immune training in bovine γδ T cells. A group of 16 pre-weaned Holstein calves (2-4 d age) were enrolled in the study and randomly assigned to vaccine and control groups (n=8/group). The vaccine group received two doses of 10 colony forming units (CFU) BCG Danish strain subcutaneously, separated by 2 weeks. The control group remained unvaccinated. Gamma delta T cells were purified from peripheral blood using magnetic cell sorting three weeks after receiving the 1 BCG dose. We observed functional changes in the γδ T cells from BCG-treated calves shown by increased IL-6 and TNF-α cytokine production in response to stimulation with LPS and PAM3CSK4. ATAC-Seq analysis of 78,278 regions of open chromatin (peaks) revealed that γδ T cells from BCG-treated calves had an altered epigenetic status compared to cells from the control calves. Differentially accessible peaks (DAP) found near the promoters of innate immunity-related genes like , , , , and were 1 to 4-fold more accessible in cells from BCG-treated calves. MOTIF enrichment analysis of the sequences within DAPs, which explores transcription factor binding motifs (TFBM) upstream of regulatory elements, revealed TFBM for Eomes and IRF-5 were among the most enriched transcription factors. GO enrichment analysis of genes proximal to the DAPs showed enrichment of pathways such as regulation of IL-2 production, T-cell receptor signaling pathway, and other immune regulatory pathways. In conclusion, our study shows that subcutaneous BCG administration in pre-weaned calves can induce innate immune memory in the form of trained immunity in γδ T cells. This memory is associated with increased chromatin accessibility of innate immune response-related genes, thereby inducing a functional trained immune response evidenced by increased IL-6 and TNF-α cytokine production.

摘要

卡介苗(BCG)疫苗已被证明可在接种个体中诱导针对结核病以外的疾病的非特异性保护,这归因于训练免疫的诱导。我们之前已经证明,BCG 给药可在小牛的混合外周血单核细胞和单核细胞中诱导先天免疫训练。γδ(γδ)T 细胞是非常规 T 细胞,具有先天和适应性免疫系统的特征。它们在外周血中的比例高于人类或啮齿动物,在牛对病原体的免疫反应中发挥重要作用。在本研究中,我们确定 BCG 给药是否诱导了牛γδ T 细胞的先天免疫训练。一组 16 头未断奶的荷斯坦小牛(2-4 日龄)被纳入研究并随机分为疫苗组和对照组(每组 8 头)。疫苗组接受两次皮下 10 菌落形成单位(CFU)丹麦卡介苗株接种,间隔 2 周。对照组未接种。在接受 1 次 BCG 剂量后 3 周,使用磁性细胞分选从外周血中纯化 γδ T 细胞。我们观察到 BCG 处理的小牛的 γδ T 细胞发生了功能变化,表现为对 LPS 和 PAM3CSK4刺激的 IL-6 和 TNF-α细胞因子产生增加。对 78278 个开放染色质区域(峰)的 ATAC-Seq 分析显示,与对照组小牛的细胞相比,BCG 处理的小牛的 γδ T 细胞具有改变的表观遗传状态。在 BCG 处理的小牛的细胞中,靠近先天免疫相关基因(如 、 、 、 和 )启动子的可及峰(DAP)的差异可及峰(DAP)发现,1 到 4 倍的可及性增加。在 DAP 内序列的 MOTIF 富集分析中,探索了调节元件上游的转录因子结合基序(TFBM),结果发现 Eomes 和 IRF-5 的 TFBM 是最丰富的转录因子之一。与 DAP 附近基因的 GO 富集分析显示,IL-2 产生的调节、T 细胞受体信号通路和其他免疫调节途径等途径的富集。总之,我们的研究表明,在未断奶的小牛中皮下给予 BCG 可诱导 γδ T 细胞中以训练免疫形式存在的先天免疫记忆。这种记忆与先天免疫反应相关基因的染色质可及性增加有关,从而诱导 IL-6 和 TNF-α细胞因子产生增加的功能性训练免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a25/11295143/198444c28a3d/fimmu-15-1423843-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a25/11295143/fcd652736ef2/fimmu-15-1423843-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a25/11295143/102f3853c86d/fimmu-15-1423843-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a25/11295143/198444c28a3d/fimmu-15-1423843-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a25/11295143/fcd652736ef2/fimmu-15-1423843-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a25/11295143/102f3853c86d/fimmu-15-1423843-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a25/11295143/198444c28a3d/fimmu-15-1423843-g003.jpg

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