Department of Immunology and Molecular Biology, University of Gondar, Gondar, Ethiopia.
The Ohio State, Global One Health, Addis Ababa, Ethiopia.
PLoS Negl Trop Dis. 2023 Jan 20;17(1):e0011094. doi: 10.1371/journal.pntd.0011094. eCollection 2023 Jan.
Interferon-γ (IFN-γ) is a key cytokine inducing protective immune responses during tuberculosis (TB) infection. Helminth-induced immune responses may affect IFN-γ production by T cells, although its connection with disease severity and immune recovery during treatment is unexplored. We investigated the species-specific effect of helminths on the IFN-γ production by T cells in relation to disease severity during active and latent TB infection (LTBI).
In this study, 69 active pulmonary TB patients (PTB), 28 with LTBI and 66 healthy controls were included. Active TB was diagnosed using GenXpert MTB/RIF while QuantiFERON test (QFT) was used for the screening of healthy community controls (CCs) and for the diagnosis of LTBI. Helminth infection was identified by routine diagnosis whereas clinical disease severity was evaluated by the TB score. Intracellular IFN-γ production of T cells in stimulated peripheral blood mononuclear cells (PBMCs) was analyzed by flow cytometry using TB antigens (PPD), the polyclonal T cell activator staphylococcal enterotoxin B (SEB), or medium as unstimulated control.
Helminth infected CCs and LTBI subjects showed a significant reduction of IFN-γ+ CD4+ T cells by PPD-stimulation compared to non-helminth infected control groups. The significant reduction in the frequency of IFN-γ+ T cells in both latent and active PTB patients following SEB stimulation was mostly attributed to Schistosoma mansoni infection, whereas Ascaris lumbricoides, Schistosoma mansoni, and hookworm infection contributed equally in CCs. Following anti-helminthic and anti-TB treatment for 2 months, the frequency of IFN-γ+ CD4 T cells in helminth coinfected PTB was restored to levels of helminth negative PTB before treatment. Helminth coinfected PTB patients with an intermediate and severe clinical course had reduced capacity for production of IFN-γ+ T cells compared to the corresponding non-helminth infected PTB.
We found a reduction in IFN-γ producing T cells by helminth coinfection which was restored following anti-helminthic treatment. This reduction was helminth species-dependent in an exploratory sub-analysis and correlated to increased disease severity.
干扰素-γ(IFN-γ)是结核分枝杆菌(TB)感染期间诱导保护性免疫反应的关键细胞因子。寄生虫诱导的免疫反应可能会影响 T 细胞产生 IFN-γ,尽管其与疾病严重程度和治疗期间的免疫恢复之间的联系尚未得到探索。我们研究了寄生虫对 T 细胞 IFN-γ产生的种特异性影响,以及在活动性和潜伏性结核感染(LTBI)期间与疾病严重程度的关系。
本研究纳入了 69 例活动性肺结核患者(PTB),其中 28 例为 LTBI 患者,66 例为健康对照者。活动性肺结核的诊断采用 GenXpert MTB/RIF,而 QuantiFERON 试验(QFT)用于健康社区对照者(CC)的筛查和 LTBI 的诊断。寄生虫感染通过常规诊断确定,而临床疾病严重程度则通过 TB 评分进行评估。通过流式细胞术分析刺激外周血单核细胞(PBMC)中 T 细胞的 IFN-γ产生,使用结核抗原(PPD)、多克隆 T 细胞激活剂葡萄球菌肠毒素 B(SEB)或未刺激对照的培养基进行刺激。
与未感染寄生虫的对照组相比,寄生虫感染的 CC 和 LTBI 患者经 PPD 刺激后 IFN-γ+CD4+T 细胞的数量显著减少。在潜伏和活动性 PTB 患者中,SEB 刺激后 IFN-γ+T 细胞的频率显著降低,主要归因于曼氏血吸虫感染,而蛔虫、曼氏血吸虫和钩虫感染在 CC 中同样重要。在进行为期 2 个月的抗寄生虫和抗结核治疗后,寄生虫合并感染的 PTB 患者的 IFN-γ+CD4 T 细胞频率恢复到治疗前无寄生虫感染的 PTB 水平。与相应的无寄生虫感染的 PTB 相比,具有中度和重度临床病程的寄生虫合并感染的 PTB 患者产生 IFN-γ+T 细胞的能力降低。
我们发现寄生虫合并感染导致 IFN-γ产生的 T 细胞减少,抗寄生虫治疗后恢复。在探索性亚分析中,这种减少与寄生虫种类有关,与疾病严重程度增加相关。