Diabetes is associated with lower tuberculosis antigen-specific interferon gamma release in Tanzanian tuberculosis patients and non-tuberculosis controls.

Daniel Faurholt-Jepsen, Martine Grosos Aabye, Andreas Vestergaard Jensen, Nyagosya Range, George Praygod, Kidola Jeremiah, John Changalucha, Maria Faurholt-Jepsen, Lotte Jensen, Signe Marie Jensen, Henrik Krarup, Pernille Ravn, Henrik Friis, Ase Bengård Andersen
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引用次数: 41

Abstract

Background: Diabetes is increasingly common in TB endemic regions and plays a role as a possible risk factor for increased progression from latent TB infection (LTBI) to active TB disease. Although the pathophysiological mechanisms are not fully understood, the immune system is weakened in diabetes patients and therefore the validity of interferon gamma release assays (IGRA) may be compromised. The aim of the present study was to assess the association between diabetes and Mycobacterium tuberculosis (Mtb) antigen-specific interferon gamma (IFN-γ) release in a TB endemic area among culture-confirmed TB patients and non-TB controls.

Methods: Culture-confirmed pulmonary TB patients (n = 187) and healthy non-TB neighbourhood controls (n = 190) from Mwanza, Tanzania were tested for the presence of circulating T cells recognizing Mtb antigens using an IGRA. The diabetes status of all participants was assessed using a standard oral glucose tolerance test. The impact of diabetes on the performance of the IGRA was estimated using robust linear and logistic regression.

Results: Compared to normal glucose tolerance, diabetes was associated with reduced levels of Mtb-specific IFN-γ. Increasing levels of fasting blood glucose (B - 0.3, 95% confidence interval - 0.6 to - 0.03, p = 0.033) was negatively associated with IFN-γ. Although TB patients had higher specific and lower unspecific mitogen IFN-γ responses compared to non-TB controls, the association between diabetes and IFN-γ did not depend on TB status.

Conclusion: Diabetes is associated with lower levels of Mtb antigen-specific IFN-γ, and the validity of IFN- γ tests for LTBI may be questionable in individuals with diabetes.

糖尿病与坦桑尼亚结核病患者和非结核病对照者较低的结核病抗原特异性干扰素γ释放有关。
背景:糖尿病在结核病流行地区越来越普遍,并可能成为潜伏性结核感染(LTBI)向活动性结核病发展的一个危险因素。虽然病理生理机制尚不完全清楚,但糖尿病患者的免疫系统减弱,因此干扰素γ释放试验(IGRA)的有效性可能受到损害。本研究的目的是评估糖尿病与结核分枝杆菌(Mtb)抗原特异性干扰素γ (IFN-γ)在结核流行区培养确诊结核患者和非结核对照者中的释放之间的关系。方法:使用IGRA检测来自坦桑尼亚Mwanza的培养确诊肺结核患者(187例)和健康的非结核病社区对照(190例)是否存在识别结核分枝杆菌抗原的循环T细胞。使用标准的口服葡萄糖耐量试验评估所有参与者的糖尿病状况。糖尿病对IGRA性能的影响使用稳健线性和逻辑回归进行估计。结果:与正常糖耐量相比,糖尿病与mtb特异性IFN-γ水平降低相关。空腹血糖水平升高(B - 0.3, 95%可信区间为- 0.6至- 0.03,p = 0.033)与IFN-γ呈负相关。尽管与非结核病对照相比,结核病患者具有更高的特异性和更低的非特异性丝裂原IFN-γ反应,但糖尿病和IFN-γ之间的关联并不取决于结核病状况。结论:糖尿病与Mtb抗原特异性IFN-γ水平降低有关,而IFN-γ检测LTBI在糖尿病患者中的有效性可能值得怀疑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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