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使用人THP-1和Jurkat细胞对H37Rv及共刺激进行研究时的细胞因子反应,以及一项人类肺结核与蠕虫共感染的初步研究。

Cytokine Responses during H37Rv and Costimulation Using Human THP-1 and Jurkat Cells, and a Pilot Human Tuberculosis and Helminth Coinfection Study.

作者信息

Bhengu Khethiwe N, Singh Ravesh, Naidoo Pragalathan, Mpaka-Mbatha Miranda N, Nembe-Mafa Nomzamo, Mkhize-Kwitshana Zilungile L

机构信息

Department of Medical Microbiology, School of Laboratory Medicine and Medical Sciences, College of Health Sciences, Nelson R. Mandela School of Medicine, University of KwaZulu-Natal, Durban 4001, South Africa.

Division of Research Capacity Development, South African Medical Research Council (SAMRC), Cape Town 7505, South Africa.

出版信息

Microorganisms. 2023 Jul 21;11(7):1846. doi: 10.3390/microorganisms11071846.

Abstract

BACKGROUND

Helminth infections are widespread in tuberculosis-endemic areas and are associated with an increased risk of active tuberculosis. In contrast to the pro-inflammatory Th1 responses elicited by (Mtb) infection, helminth infections induce anti-inflammatory Th2/Treg responses. A robust Th2 response has been linked to reduced tuberculosis protection. Several studies show the effect of helminth infection on BCG vaccination and TB, but the mechanisms remain unclear.

AIM

To determine the cytokine response profiles during tuberculosis and intestinal helminth coinfection.

METHODS

For the in vitro study, lymphocytic Jurkat and monocytic THP-1 cell lines were stimulated with Mtb H37Rv and () excretory-secretory protein extracts for 24 and 48 h. The pilot human ex vivo study consisted of participants infected with Mtb, helminths, or coinfected with both Mtb and helminths. Thereafter, the gene transcription levels of IFN-γ, TNF-α, granzyme B, perforin, IL-2, IL-17, NFATC2, Eomesodermin, IL-4, IL-5, IL-10, TGF-β and FoxP3 in the unstimulated/uninfected controls, singly stimulated/infected and costimulated/coinfected groups were determined using RT-qPCR.

RESULTS

TB-stimulated Jurkat cells had significantly higher levels of IFN-γ, TNF-α, granzyme B, and perforin compared to unstimulated controls, LPS- and -stimulated cells, and plus TB-costimulated cells ( < 0.0001). IL-2, IL-17, Eomes, and NFATC2 levels were also higher in TB-stimulated Jurkat cells ( < 0.0001). Jurkat and THP-1 cells singly stimulated with TB had lower IL-5 and IL-4 levels compared to those singly stimulated with and those costimulated with TB plus ( < 0.0001). -singly stimulated cells had higher IL-4 levels compared to TB plus -costimulated Jurkat and THP-1 cells ( < 0.0001). TGF-β levels were also lower in TB-singly stimulated cells compared to TB plus -costimulated cells ( < 0.0001). IL-10 levels were lower in TB-stimulated Jurkat and THP-1 cells compared to TB plus -costimulated cells ( < 0.0001). Similar results were noted for the human ex vivo study, albeit with a smaller sample size.

CONCLUSIONS

Data suggest that helminths induce a predominant Th2/Treg response which may downregulate critical Th1 responses that are crucial for tuberculosis protection.

摘要

背景

蠕虫感染在结核病流行地区广泛存在,且与活动性结核病风险增加相关。与结核分枝杆菌(Mtb)感染引发的促炎性Th1反应不同,蠕虫感染诱导抗炎性Th2/Treg反应。强烈的Th2反应与结核病保护作用降低有关。多项研究显示了蠕虫感染对卡介苗接种和结核病的影响,但其机制仍不清楚。

目的

确定结核病与肠道蠕虫合并感染期间的细胞因子反应谱。

方法

在体外研究中,用Mtb H37Rv和[蠕虫名称未给出]排泄分泌蛋白提取物刺激淋巴细胞Jurkat和单核细胞THP-1细胞系24小时和48小时。初步人体离体研究包括感染Mtb、蠕虫或同时感染Mtb和蠕虫的参与者。此后,使用RT-qPCR测定未刺激/未感染对照组、单独刺激/感染组和共刺激/合并感染组中IFN-γ、TNF-α、颗粒酶B、穿孔素、IL-2、IL-17、NFATC2、胚外中胚层决定蛋白、IL-4、IL-5、IL-10、TGF-β和FoxP3的基因转录水平。

结果

与未刺激对照组、脂多糖和[蠕虫名称未给出]刺激的细胞以及[蠕虫名称未给出]加结核分枝杆菌共刺激的细胞相比,结核分枝杆菌刺激的Jurkat细胞中IFN-γ、TNF-α、颗粒酶B和穿孔素水平显著更高(P<0.0001)。结核分枝杆菌刺激的Jurkat细胞中IL-2、IL-17、胚外中胚层决定蛋白和NFATC2水平也更高(P<0.0001)。与单独用[蠕虫名称未给出]刺激的细胞以及用结核分枝杆菌加[蠕虫名称未给出]共刺激的细胞相比,单独用结核分枝杆菌刺激的Jurkat和THP-1细胞中IL-5和IL-4水平更低(P<0.0001)。单独用[蠕虫名称未给出]刺激的细胞比用结核分枝杆菌加[蠕虫名称未给出]共刺激的Jurkat和THP-1细胞中IL-4水平更高(P<0.0001)。与结核分枝杆菌加[蠕虫名称未给出]共刺激的细胞相比,单独用结核分枝杆菌刺激的细胞中TGF-β水平也更低(P<0.0001)。与结核分枝杆菌加[蠕虫名称未给出]共刺激的细胞相比,结核分枝杆菌刺激的Jurkat和THP-1细胞中IL-10水平更低(P<0.0001)。人体离体研究也得到了类似结果,尽管样本量较小。

结论

数据表明,蠕虫诱导主要的Th2/Treg反应,这可能下调对结核病保护至关重要的关键Th1反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d989/10384037/de4afe897ff1/microorganisms-11-01846-g001.jpg

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