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在涂片阴性结核病患者中,结核分枝杆菌特异性 CD4 T 细胞持续表达激活标志物。

Persistent expression of activation markers on Mycobacterium tuberculosis-specific CD4 T cells in smear negative TB patients.

机构信息

Department of Medical Laboratory Science, College of Health Sciences, Debre Markos University, Addis Ababa, Ethiopia.

Department of Microbiology, Immunology and Parasitology, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.

出版信息

PLoS One. 2022 Aug 30;17(8):e0271234. doi: 10.1371/journal.pone.0271234. eCollection 2022.

Abstract

BACKGROUND

T cell activation (HLA-DR, CD-38), proliferation (KI-67), and functional (IFN-γ, TNF-α) markers have recently been shown to be useful in predicting and monitoring anti-TB responses in smear positive TB, but previous research did not characterize the activation and proliferation profiles after therapy of smear negative TB.

METHODOLOGY

In this study, we used polychromatic flow cytometry to assess selected PPD-specific T cell markers using fresh PBMC of smear negative and positive pulmonary tuberculosis (PTB) patients, recruited from health facilities in Addis Ababa.

RESULT

Levels of activation (HLA-DR, CD38) and proliferation (Ki-67) among total unstimulated CD4 T cells decreased significantly after therapy, particularly at month 6. Similarly, levels of PPD-specific T cell activation markers (HLA-DR, CD-38) were significantly lower in smear positive PTB patients following treatment, whereas a consistent decline in these markers was less apparent among smear negative PTB patients at the sixth month.

CONCLUSION

After six months of standard anti-TB therapy, persistent levels of activation of HLA-DR and CD-38 from PPD specific CD4+T cells in this study could indicate that those markers have little value in monitoring and predicting anti-TB treatment response in smear negative pulmonary TB patients in Ethiopian context.

摘要

背景

T 细胞激活(HLA-DR、CD-38)、增殖(KI-67)和功能(IFN-γ、TNF-α)标志物最近已被证明可用于预测和监测涂片阳性结核病中的抗结核反应,但以前的研究并未描述涂阴结核病治疗后 T 细胞的激活和增殖特征。

方法

本研究采用多色流式细胞术,使用来自亚的斯亚贝巴医疗机构的涂阴和涂阳肺结核(PTB)患者新鲜 PBMC 评估了 PPD 特异性 T 细胞标志物。

结果

治疗后,总未刺激 CD4 T 细胞的激活(HLA-DR、CD38)和增殖(Ki-67)水平显著下降,尤其是在 6 个月时。同样,治疗后涂阳 PTB 患者的 PPD 特异性 T 细胞激活标志物(HLA-DR、CD-38)水平显著降低,而涂阴 PTB 患者在第 6 个月时这些标志物的下降则不太明显。

结论

在标准抗结核治疗 6 个月后,本研究中 PPD 特异性 CD4+T 细胞中 HLA-DR 和 CD-38 的持续激活水平表明,这些标志物在监测和预测埃塞俄比亚涂阴肺结核患者的抗结核治疗反应方面价值不大。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd47/9426896/89b890894d35/pone.0271234.g001.jpg

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