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Oxidative stress response in regulatory and conventional T cells: a comparison between patients with chronic coronary syndrome and healthy subjects
Journal of Translational Medicine volume 19, Article number: 241 (2021)
Inflammation and oxidative stress form a vicious circle in atherosclerosis. Oxidative stress can have detrimental effects on T cells. A unique subset of CD4+ T cells, known as regulatory T (Treg) cells, has been associated with atheroprotective effects. Reduced numbers of Treg cells is a consistent finding in patients with chronic coronary syndrome (CCS). However, it is unclear to what extent these cells are sensitive to oxidative stress. In this pilot study, we tested the hypothesis that oxidative stress might be a potential contributor to the Treg cell deficit in CCS patients.
Thirty patients with CCS and 24 healthy controls were included. Treg (CD4+CD25+CD127−) and conventional T (CD4+CD25−, Tconv) cells were isolated and treated with increasing doses of H2O2. Intracellular ROS levels and cell death were measured after 2 and 18 h, respectively. The expression of antioxidant genes was measured in freshly isolated Treg and Tconv cells. Also, total antioxidant capacity (TAC) was measured in fresh peripheral blood mononuclear cells, and oxidized (ox) LDL/LDL ratios were determined in plasma.
At all doses of H2O2, Treg cells accumulated more ROS and exhibited higher rates of death than their Tconv counterparts, p < 0.0001. Treg cells also expressed higher levels of antioxidant genes, including thioredoxin and thioredoxin reductase-1 (p < 0.0001), though without any differences between CCS patients and controls. Tconv cells from CCS patients were, on the other hand, more sensitive to oxidative stress ex vivo and expressed more thioredoxin reductase-1 than Tconv cells from controls, p < 0.05. Also, TAC levels were lower in patients, 0.97 vs 1.53 UAE/100 µg, p = 0.001, while oxLDL/LDL ratios were higher, 29 vs 22, p = 0.006.
Treg cells isolated from either CCS patients or healthy controls were all highly sensitive to oxidative stress ex vivo. There were signs of oxidant-antioxidant imbalance in CCS patients and we thus assume that oxidative stress may play a role in the reduction of Treg cells in vivo.
Oxidative stress and chronic inflammation are closely linked phenomena that can perpetuate each other and easily form a vicious circle in chronic disease. The simultaneous existence of oxidative stress and low-grade inflammation in atherosclerosis is well established. Oxidative stress, defined as chronic overproduction of reactive oxygen species (ROS) or rather an imbalance between oxidants and antioxidants in favor of the oxidants , plays a major role in the development of atherosclerosis [2, 3]. In humans, a variety of circulating markers of oxidative stress, including oxidative modification of low density lipoprotein (LDL), have shown associations with cardiovascular disease [4, 5]. It has also been shown that oxidized (ox) LDL can elicit a robust immune response in atherosclerosis, involving activation of CD4+ T cells .
Although moderate levels of ROS are necessary for the proper regulation of T cell activation, large quantities of ROS may have detrimental effects on T cells, such as decreased viability . This may be an area of special interest in understanding the T cell perturbations associated with coronary artery disease. The systemic T cell activation that occurs in many patients with acute coronary syndrome (ACS) does not normalize over time but becomes persistent, despite clinical stability and medical treatment [8,9,10].
The perturbed T cell repertoire in patients with coronary artery disease is also associated with a decrease of regulatory T (Treg) cells, a specialized subpopulation of CD4+CD25+ T cells. These cells were first identified in 1995 by Sakaguchi et al.  as a subset of thymus-derived CD4+ T cells that expressed high levels of the interleukin (IL-2) receptor α-chain CD25 and protected thymectomized mice from autoimmunity. In humans, several autoimmune and inflammatory pathologies have been associated with numerical deficits in Treg cells as well as increased apoptosis of Treg cells [12,13,14]. Interestingly, Treg cell deficits have also been reported in patients with ACS as well as in those with CCS, the latter a term defining patients with stable coronary artery disease [9, 15,16,17]. Whether Treg cells can function as new targets in atherosclerotic disease has become a subject of increasing interest . However, it is still unclear why Treg cells are reduced in patients with coronary artery disease but one intriguing possibility is that oxidative stress plays a major role. In a previous study, Mor et al.  demonstrated that the numbers of CD4+CD25+ Treg cells were markedly reduced after incubation with oxLDL while the effect on conventional CD4+CD25− T (Tconv) cells was negligible. The finding indicating that Treg cells were more sensitive to oxidative stress compared to Tconv cells was however contradicted by Mougiakakos et al.  who showed that Treg cells from healthy volunteers were more resistant to hydrogen peroxide (H2O2)-induced cell death compared to Tconv cells.
The extent to which oxidative stress affects Treg cell survival in coronary artery disease is thus far from clarified. In this pilot study, we tested the hypothesis that oxidative stress is a contributor to the Treg cell deficit in CCS patients. Our first aim was to perform a comparison between Treg and Tconv cells with respect to sensitivity towards oxidative stress. A second aim was to investigate whether Treg and Tconv cells from CCS patients and healthy controls differed in their sensitivity towards oxidative stress. Different aspects of oxidative stress response were examined in freshly isolated Treg and Tconv cells. We studied the sensitivity to oxidative stress-induced cell death ex vivo by treating cells with H2O2, a major member of the ROS family. We also determined the impact of H2O2 on cellular oxidative stress by measuring total (cytoplasmic and nuclear) cellular ROS at the single cell level. To further elucidate the oxidative stress response in vivo, we measured the expression and secretion of endogenous antioxidants in Treg and Tconv cells from patients and controls.
The study population consisted of patients (n = 30) recruited from the Department of Cardiology, University Hospital, Linköping, Sweden, as well as control subjects with approximately equal sex and age distribution (n = 24). All patients had significant coronary artery disease, defined as ≥ 50% luminal narrowing in any of the major epicardial coronary arteries (i.e., the right coronary artery, left anterior descending artery, and left circumflex artery), and a history of coronary event, i.e. ACS or stable angina followed by coronary revascularization. For the control group, individual residents of Linköping were randomly selected from the Swedish Population Register and invited to participate in the study. Individuals who accepted the invitation were included as controls if they were anamnestically healthy and had normal routine laboratory tests. Use of lipid-lowering or antihypertensive drugs for primary prevention of cardiovascular disease was allowed in the control group.
Study subjects were excluded if they suffered from severe heart failure, immunological disorders, neoplastic disease, had evidence of acute or recent (< 2 months) infection or major trauma, had undergone surgery/revascularization procedure (< 2 months) or received regular treatment with immunosuppressive or anti-inflammatory agents (except low-dose aspirin).
Peripheral blood mononuclear cells (PBMCs) were isolated from diluted sodium heparinized whole blood using Ficoll-Paque Density Gradient Medium (ThermoFisher Scientific) as previously described . An EasySep Human CD4+CD127lowCD25+ Regulatory T Cell Isolation Kit (STEMCELL Technologies) was used according to manufacturer´s instructions on PBMCs resulting in two cell fractions; Treg cells defined as CD4+CD127lowCD25+ and Tconv cells defined as CD4+CD127+CD25− T cells. After isolation cells were resuspended in complete RPMI (Fisher Scientific) with 10% FBS (Fisher Scientific) and 2% Penicillin Streptomycin solution (Fisher Scientific).
For purity checks, cells were stained with a Human Regulatory T Cell Sorting Kit cocktail including CD45RA-FITC, CD127-Alexa Fluor647, CD25-PE, and CD4-PerCP-Cy5.5 (BD Biosciences) and analysed on a FACS aria (BD Biosciences). Cells were separately stained for FoxP3 expression using a Human FoxP3 Buffer Set (BD Biosciences) together with antibodies against CD4-FITC and FoxP3-V450 and analysed with Gallios flow cytometer (Beckman Coulter). Illustrative results are shown in Additional file 1: Figure S1.
H2O2-induced cell death of Treg and Tconv cells
A total of 40,000 Treg or Tconv cells were treated with 5, 10, 20, or 30 μM H2O2 or left untreated in a total volume of 200 μL in a round-bottom 96-well plate. Cells were incubated for 18 h in a humified incubator at 37 °C and 5% CO2. The incubation time was chosen based on previous similar studies [19, 21]. Following incubation, cells were washed and 100 µL Annexin-V Binding Buffer (BD Biosciences), Annexin-V PE and CD4-BV510 antibodies (BD Biosciences) was added. After 15 min 400 µL Annexin-V Binding Buffer and SYTOX Red Dead Cell Stain (ThermoFisher) was added. After another 10 min, cells were analyzed within 1 h with a Gallios flow cytometer to monitor cell death.
Staurosporin-induced cell apoptosis of Tregand Tconv cells
In the same manner as described above, Treg and Tconv cell fractions were also treated with 2.5 µM staurosporin (STS) (Streptomyces sp. Origin, Sigma-Aldrich) as an alternative way to induce apoptosis.
H2O2-induced intracellular ROS levels in Treg and Tconv cells
A total of 40 000 Treg or Tconv cells were treated with 30 µM, 60 µM and 120 µM H2O2 at 37 °C for a total of 2 h. After 1 h, CellROX Green (Thermofisher), a measure of total (cytoplasmic and nuclear) cellular ROS, was added. Thereafter cells were washed with PBS + O.5% FBS and and resuspended in 100 µL PBS + 0.5% FBS and SYTOX Red Dead Cell Stain, CD4BV510 and 10 µL Brilliant Stain Buffer (BD Biosciences) were added and kept for 15 in in the dark in room temperature. Finally, mean fluorescence intensity (MFI) of CellROX Green was recorded with a 3-laser Gallios Flow Cytometer.
Flow cytometry analyses
Flow cytometry data were analyzed with Kaluza Analysis Software 2.1 (Beckman Coulter). Lymphocytes were gated according to size and granularity and thereafter CD4+ cells only were gated. Annexin-V identified early apoptosis while SYTOX identified late apoptosis and necrosis. An illustrative example is shown in Additional file 2: Figure S2. Cells negative for Annexin-V and SYTOX were considered viable. For the oxidative stress assay, cells were gated in a lymphocyte gate and the CellROX Green signal was recorded in CD4+ cells that were negative for SYTOX, i.e. living cells.
Oxidative stress gene expression in circulating Treg and Tconv cells
mRNA expression of oxidative stress-associated genes was assessed in Treg and Tconv cells isolated from PBMCs using the same kit from STEMCELL as described above. Cell lysates were collected directly after isolation. Total RNA was isolated using Qiagen total RNA isolation kit (Thermofisher). The RNA (total 21,6 ng) was converted to cDNA using high capacity cDNA reverse transcription kit with an RNAse inhibitor (Life Technologies). cDNA was amplified by RT-PCR reactions with TaqMan™ Fast Universal PCR Mastermix (Life Technologies) on an ABI 7500 Sequence Detector (Applied Biosystems). The following TaqMan Gene Expression Assay kits were used: Hs00167309_m1 for superoxide dismutase 2 (SOD2), Hs00156308_m1 for catalase (CAT), Hs00757844_m1 for oxidation resistance 1 (OXR1), Hs04194449_s1 for glutathione peroxidase-7 (GPX7), Hs00828652_m1 for thioredoxin (Trx), Hs00917067_m1 thioredoxin reductase (TrxR1). Eukaryotic 18S rRNA (Part number: 4352930E) served as endogenous control. The expression of all genes was calculated with the comparative CT method where the amount of target, normalized to an endogenous reference and relative to a calibrator, is given by 2ΔΔCT according to the user bulletin no 2 (Applied Biosystems). Results are presented as arbitrary units. Each sample was run in duplicates and a maximum deviation of 10% was allowed.
TrxR1 in cell supernatants
The concentration of TrxR1 in cell supernatants from Treg and Tconv cells after treatment with or without 30 μM H2O2 for 18 h was measured with an ELISA kit (Abcam, UK) according to manufacturer´s instructions. The range of the standard curve was 0.196–25 ng/mL. Samples were assayed in duplicates and a maximal deviation of 15% was allowed. Undetected samples were given half the value of the lowest standard point.
Total antioxidant capacity in PBMCs
Total antioxidant capacity (TAC) in PBMCs was measured using Cell Biolabs, Inc. OxiSelect Total Antioxidant Capacity Assay Kit. In brief, cell pellets of 3 millions PBMCs were snap frozen and stored in − 80 °C for no longer than 2 weeks. Frozen PBMCs were lysed by thawing on ice followed by water-bath sonication for 10 min and thereafter kept on ice. The TAC assays were then performed according to manufacturer’s instructions. Results are expressed as units of uric acid equivalents (UAE).The TAC results were also normalized by protein amount measured in PBMCs using Thermo Scientific’s Coomassie Plus (Bradford) Assay Kit according to the manufacturer’s instruction. The final TAC results were calculated according to the equation below:
Oxidized LDL cholesterol in plasma
OxLDL in EDTA plasma was measured by an ELISA (Mercodia, Uppsala, Sweden), which is a capture ELISA using the mAb-4E6 antibody against a conformational epitope in oxidized ApoB-100, developed by Holvoet et al.. The inter-assay variation was below 5% for the oxLDL ELISA. All samples were within the range of detection. The oxLDL/LDL ratio was used as an estimate of in vivo LDL oxidation .
Statistical analyses were calculated in IBM SPSS Statistics 25. Groups and independent variables were compared using independent Mann–Whitney U tests, Fisher´s exact test, and a Chi Square test. Wilcoxon rank sum test or paired t-test were used to compare paired data. Correlations were calculated using Spearman rank correlation test. Numeric data are presented as median and inter-quartile range. A p value < 0.05 was considered significant. Sample size calculation was based on a previous study showing that natural killer cells in CCS patients were more sensitive to apoptosis induced by oxidized lipids compared to natural killer cells in healthy controls .
Characteristics of study population
The basal characteristics of the study population are presented in Table 1. There were no significant differences between CCS patients and controls with respect to age, gender, body mass index, current smoking, use of anti-hypertensive medication or laboratory variables, including high density lipoprotein (HDL) cholesterol, triglycerides, creatinine or fasting glucose levels. The prevalence of former smoking was higher among patients. Seven (23%) patients had type 2 diabetes. Twenty-three (77%) patients had a history of ACS. As regards coronary revascularization, 19 (63%) patients had a history of percutaneous coronary intervention (PCI), 15 (50%) had a history of coronary artery bypass grafting (CABG) while 4 (13%) had a history of previous PCI followed by CABG. Statins were used by all patients (except for one) resulting in significantly lower LDL levels in this group. Also, the levels of oxLDL were lower in patients. However, the oxLDL/LDL ratios were significantly higher indicating an environment of oxidative stress in the patient group. Moreover, the TAC levels in PBMCs were significantly lower in patients compared to controls, p = 0.001. When the 7 patients with diabetes were excluded, the TAC levels were still significantly lower in patients, p = 0.002.
H2O2- and STS-induced cell death of Treg and Tconv cell
Treg and Tconv cells were isolated from 34 subjects (20 CCS patients and 14 controls). Among patients, 16 had a history of ACS (7 PCI, 9 CABG, 4 PCI followed by CABG) and 4 had a history of stable angina (2 PCI, 2 CABG). Separate fractions of Treg and Tconv cells were treated with medium only or increasing concentrations of H2O2. Before treatment, the viability was > 90% in both cell types. After 18 h incubation with medium only, the proportions of living Treg cells were significantly lower compared with Tconv cells, 71 (64–76) % vs 90 (86–93) %, p < 0.001. At all concentrations of H2O2, Treg cells were more susceptible to H2O2-induced cell death than Tconv cells (Fig. 1A). There was a clear dose–response relationship with very low percentages of living Treg cells at 20 and 30 μM H2O2.
Treg cells were also more susceptible to cell death compared to Tconv cells when STS, a classical inducer of the intrinsic apoptotic pathway, was used. The proportions of living cells were 46 (37–54) % and 88 (79–95) %, p < 0.001, for Treg and Tconv cells, respectively, after treatment with 2.5 µM STS.
There were no significant differences in susceptibility to H2O2-induced cell death between Treg cells from CCS patients and Treg cells from controls at any concentration of H2O2 (Table 2). Neither were there any differences in STS-induced cell death in Treg cells between patients and controls. On the other hand, the percentages of living Tconv cells were significantly lower in patients than in controls when Tconv cells were exposed to H2O2 at lower concentrations (5 or 10 µM) or to STS (Table 2).
H2O2-induced intracellular ROS accumulation in Treg and Tconv cells
H2O2-induced intracellular ROS levels were measured in Treg and Tconv cells after 2 h treatment in medium with or without increasing concentrations of H2O2. Treatment with medium only or with 10 µM H2O2 did not reveal any differences between Treg and Tconv cells regardless of subject types while the ROS accumulation was significantly larger in Treg cells treated with 30 µM H2O2 or more (Fig. 1B). When we compared CCS patients and controls, the ROS production in Treg and Tconv cells did not show any significant differences (Additional file 3: Figures S3A and B).
The in vivo expression of oxidative stress-associated genes in Treg and Tconv cells
In order to compare the oxidative stress response in vivo, we measured the expression of a number of oxidative stress-associated genes in freshly isolated Treg and Tconv cells from 20 subjects, 10 CCS patients (8 males, 2 females, median age 67, 7 with a previous history of ACS and 4 with a history of CABG) and 10 controls (8 males, 2 females, median age 68). As shown in Fig. 2A, the mRNA levels of CAT, OXR1, Trx and TrxR1 were significantly higher in Treg cells than in Tconv cells regardless of subject types while mRNA levels of GPX7 and SOD2 expression did not differ between the two T cell fractions (Fig. 2B).
When comparing CCS patients and controls, the Treg cells did not show any significant differences in gene expression (Table 3). On the other hand, the Tconv cells from CCS patients showed significantly higher expression of TrxR1 than those from controls (p = 0.033). Also, the Trx and SOD2 mRNA levels tended to be higher in Tconv cells from patients (p = 0.104 and p = 0.091, respectively).
Secretion of TrxR1 by Treg and Tconv cells
In order to further confirm the changes in gene expression, we measured TrxR1 protein levels in supernatants from Treg and Tconv cells collected from 32 subjects (18 CCS patients and 14 controls). The reason for measuring TrxT1 relied on a previous study by Xie et al. . The Trx1 levels were generally low and almost undetectable in untreated samples. However, both Treg and Tconv cells secreted significantly more TrxR1 after H2O2 treatment, p < 0.0001 in both cell types. Also, TrxR1 levels were significantly higher in supernatants from Treg cells compared to Tconv cells, p = 0.003 (Fig. 2C). There were no differences between CCS patients and controls (Additional file 3: Figure S3).
There were significant inverse relationships between H2O2-induced intracellular ROS levels and % of living cells after 18 h, in particular for Tconv cells (Table 4). There was no correlation between intracellular ROS levels and STS-induced cell death. We were not able to study correlations between susceptibility to H2O2 ex vivo and antioxidant gene expression since these analyses were performed in different study subjects.
TAC levels in freshly isolated PBMCs were measured in all study subjects and correlated inversely with intracellular ROS levels after 2 h treatment with 60 µM H2O2 in Treg cells, r = − 0.480, p = 0.037; and Tconv cells, r = − 0.511, p = 0.030, but showed no correlations with H2O2-induced cell death ex vivo or with antioxidant gene expression.
The main findings from the present study are that human Treg cells exhibit markedly increased sensitivity to H2O2-induced ROS production and cell death compared to Tconv cells in both CCS patients and healthy controls. Treg cells were also more sensitive to spontaneous cell death when cultured in medium overnight and to cell death induced by STS, a potent inducer of apoptosis. Hitherto, the impact of oxidative stress on human Treg cells has been far from clarified. The existing literature is both sparse and inconsistent. Mor et al.  reported that the number of Treg cells was reduced to a considerably larger extent than the number of Tconv cells after in vitro incubation with oxidized LDL. They further showed that this effect was attenuated in the presence of caspase inhibitor suggesting that apoptosis contributed to the loss of cells. Several other studies have demonstrated that Treg cells are more prone to apoptosis than Tconv cells when they are cultured in medium only [26,27,28]. On the other hand, Mougiakakos et al.  treated T cells with 5, 10 or 20 μM H2O2 for 18 h and found that Treg cells were significantly more resistant to H2O2-induced cell death compared to Tconv cells. Moreover, they found that naïve Treg cells were more resistant than memory Treg cells. One possible explanation for the contradictory results may be the choice of study subjects. Mougiakakos et al.  used cells from a few healthy donors of unknown age while we used cells from sick and elderly subjects. Ageing and cardiovascular disease are both linked to elevated oxidative stress. We previously showed that naïve Treg cells constituted only 15% of all Treg cells in elderly CAD patients as opposed to 25% in age-matched controls, and also that the function of naïve as well as memory Treg cells was impaired in patients, including lower suppressive capacity . Differences in naïve Treg cell pool size and function as well as individual variations in oxidative status may thus contribute to the disparity in results between our study and Mougiakakos et al. . Still, important methodological aspects make it difficult to directly compare the studies. Mougiakakos et al.  used a different Treg cell isolation protocol and they assessed cell death by labelling late apoptotic and necrotic cells, while we also included labelling of early apoptotic cells.
In an attempt to assess intrinsic ability of the cells to counteract oxidative stress, we measured the mRNA expression of several main antioxidant genes which all contribute to inactivate ROS, in freshly isolated Treg and Tconv cells from both patients and controls. Collectively, the expression of catalase was significantly higher in Treg cells than in Tconv cells and so was the expression of OXR1, a protein that has been described as a cellular oxidative stress sensor regulating the expression of several antioxidant enzymes . Also, mRNA levels of the two main proteins, Trx and TrxR1, in the antioxidant Trx system were markedly upregulated in Treg cells. Our findings partly agree with the previous study by Mougiakakos et al. , who reported that Trx expression was higher in Treg cells compared with Tconv cells while, on the other hand, catalase expression did not differ in their small study group of volunteers. An earlier genomic and proteomic screening study examined the H2O2-induced gene and protein expression in human skin fibroblasts and reported that TrxR1 was the only oxidation-related candidate with elevated levels at both the mRNA and protein level, the latter measured in cell lysates . Another study by Söderberg et al.  provided evidence that TrxR1 was secreted by human PBMCs upon inflammatory stimulation. Here, we were able to show that TrxR1 was secreted into the cell supernatant to a greater extent by Treg cells than by Tconv cells upon H2O2 treatment. Altogether, our findings indicate that Treg cells have a higher endogenous antioxidant capacity than Tconv cells in both CCS patients and controls.
Several studies have reported reduced levels of Treg cells in peripheral blood of patients with ACS [9, 15,16,17]. It has also been proposed that oxidative stress is involved in the depletion of Treg cells. Mor et al.  showed that Treg cells from ACS patients were more sensitive to oxidized LDL than Treg cells from CCS patients or patients with normal coronary angiograms. A later study by Zhang et al.  showed that the spontaneous apoptosis of Treg cells was pronounced in ACS patients and further demonstrated that oxLDL was able to induce apoptosis of human Treg cells in vitro, yet without comparing Treg and Tconv cells. Recently, we found that the numerical and functional Treg cell deficit in ACS patients was not merely a transient phenomenon but that it remained after clinical stabilization . In the present study, we therefore focused on the potential role of oxidative stress in the depletion of Treg cells in CCS patients. However, there was no proof that Treg cells from patients were more prone to H2O2-induced cell death than Treg cells from controls, when assessed ex vivo. Moreover, the expression of antioxidant genes in freshly isolated Treg cells from patients and controls indicated that Treg cells in CCS patients and controls had similar levels of endogenous antioxidant enzymes in vivo. However, the significantly lower intrinsic TAC levels in PBMC from CCS patients compared with PBMC from controls pointed toward an oxidant-antioxidant imbalance in patients, highlighting the possible impact of exogenous environmental factors, such as sedentary lifestyle and unhealthy diet. The TAC assay is a copper-based assay which measures a large range of lipophilic or thiol-based antioxidants and antioxidant macromolecules but not the antioxidant enzymes discussed above [31, 32]. As a further evidence of oxidant-antioxidant imbalance, we found that the oxLDL/LDL ratios were significantly higher in the patient group indicating a higher degree of oxdation in their LDL particles. Therefore, given the high susceptibility of Treg cells to oxidative stress, it is reasonable to assume that the numbers of Treg cells may be affected by the prooxidant state in CCS patients.
Interestingly, our results indicate that Tconv cells from CCS patients were affected to a greater extent by oxidative stress than Tconv cells from controls. Tconv cells from CCS patients were more prone to undergo cell death when treated with H2O2 or STS and they also expressed significantly higher levels of TrxR1. It is well documented that the proatherogenic T cell response in atherosclerotic lesions is reflected in peripheral blood . In ACS patients, systemic T cell activation is associated with plaque instability and thrombus formation but there is also consistent evidence that the T cell activation persists after clinical stabilization [8,9,10]. T cell activation is accompanied by the release of ROS which in turn leads to an upregulation of endogenous antioxidants . Moreover, the induction of Trx and TrxR1 in T cells upon activation was recently suggested to be a critical pathway controlling T cell activation and expansion . We believe that the increased susceptibility to oxidative stress in Tconv cells from patients reflects a CD4+ T cell activation that remains in CCS patients despite clinical stability and medical treatment.
A couple of limitations should be considered in this pilot study. One limitation is the limited number of patients and controls per experimental set-up, permitting only cautious conclusions about differences between the two groups. The yield levels of Treg cells in the subjects, particularly in the CCS patients, were not high enough to allow ex vivo experiments and gene expression analyses to be carried out in the same individuals, nor to perform functional assays. Gene expression analyses were therefore performed in a separate group of subjects, 10 patients and 10 controls, though with similar characteristics as the other subjects. Another potential limitation is that the ex vivo model, where isolated fractions of T cell subsets are exposed to increasing doses of H2O2 for a relatively short period of time, may not reflect chronic inflammation.
Treg cells were highly susceptible to oxidative stress and cell death ex vivo. Treg cells also expressed and secreted high levels of antioxidants indicating a high endogenous capacity to counteract oxidative stress in both CCS patients and controls. Given the presence of oxidant-antioxidant imbalance in the patient group, we postulate that oxidative stress may be a contributor to the Treg cell deficit in vivo.
Availability of data and materials
All datasets used and analyzed throughout the study are available from the corresponding author based on sensible request.
Jones DP. Redefining oxidative stress. Antioxid Redox Signal. 2006;8:1865–79.
Kattoor AJ, Pothineni NVK, Palagiri D, Mehta JL. Oxidative stress in atherosclerosis. Curr Atheroscler Rep. 2017;19:42.
Madamanchi NR, Vendrov A, Runge MS. Oxidative stress and vascular disease. Arterioscler Thromb Vasc Biol. 2005;25:29–38.
Ho E, Karimi Galougahi K, Liu CC, Bhindi R, Figtree GA. Biological markers of oxidative stress: applications to cardiovascular research and practice. Redox Biol. 2013;1:483–91.
Patel RS, Ghasemzadeh N, Eapen DJ, Sher S, Arshad S, Ko YA, Veledar E, Samady H, Zafari AM, Sperling L, et al. Novel biomarker of oxidative stress is associated with risk of death in patients with coronary artery disease. Circulation. 2016;133:361–9.
Gisterå A, Hansson GK. The immunology of atherosclerosis. Nat Rev Nephrol. 2017;13:368–80.
Yarosz EL, Chang CH. The role of reactive oxygen species in regulating T cell-mediated immunity and disease. Immune Netw. 2018;18:e14.
Ammirati E, Moroni F, Magnoni M, Camici PG. The role of T and B cells in human atherosclerosis and atherothrombosis. Clin Exp Immunol. 2015;179:173–87.
Hasib L, Lundberg AK, Zachrisson H, Ernerudh J, Jonasson L. Functional and homeostatic defects of regulatory T cells in patients with coronary artery disease. J Intern Med. 2016;279:63–77.
Lundberg AK, Jonasson L, Hansson GK, Mailer RKW. Activation-induced FOXP3 isoform profile in peripheral CD4+ T cells is associated with coronary artery disease. Atherosclerosis. 2017;267:27–33.
Sakaguchi S, Sakaguchi N, Asano M, Itoh M, Toda M. Immunologic self-tolerance maintained by activated T cells expressing IL-2 receptor alpha-chains (CD25). Breakdown of a single mechanism of self-tolerance causes various autoimmune diseases. J Immunol. 1995;155:1151–64.
Grant CR, Liberal R, Mieli-Vergani G, Vergani D, Longhi MS. Regulatory T-cells in autoimmune diseases: challenges, controversies and–yet–unanswered questions. Autoimmun Rev. 2015;14:105–16.
John K, Hardtke-Wolenski M, Jaeckel E, Manns MP, Schulze-Osthoff K, Bantel H. Increased apoptosis of regulatory T cells in patients with active autoimmune hepatitis. Cell Death Dis. 2017;8:3219.
Veltkamp C, Anstaett M, Wahl K, Möller S, Gangl S, Bachmann O, Hardtke-Wolenski M, Länger F, Stremmel W, Manns MP, et al. Apoptosis of regulatory T lymphocytes is increased in chronic inflammatory bowel disease and reversed by anti-TNFα treatment. Gut. 2011;60:1345–53.
Emoto T, Sasaki N, Yamashita T, Kasahara K, Yodoi K, Sasaki Y, Matsumoto T, Mizoguchi T, Hirata K. Regulatory/effector T-cell ratio is reduced in coronary artery disease. Circ J. 2014;78:2935–41.
Mor A, Luboshits G, Planer D, Keren G, George J. Altered status of CD4(+)CD25(+) regulatory T cells in patients with acute coronary syndromes. Eur Heart J. 2006;27:2530–7.
Zhang WC, Wang J, Shu YW, Tang TT, Zhu ZF, Xia N, Nie SF, Liu J, Zhou SF, Li JJ, et al. Impaired thymic export and increased apoptosis account for regulatory T cell defects in patients with non-ST segment elevation acute coronary syndrome. J Biol Chem. 2012;287:34157–66.
Albany CJ, Trevelin SC, Giganti G, Lombardi G, Scottà C. Getting to the heart of the matter: the role of regulatory T-cells (Tregs) in cardiovascular disease (CVD) and atherosclerosis. Front Immunol. 2019;10:2795.
Mougiakakos D, Johansson CC, Kiessling R. Naturally occurring regulatory T cells show reduced sensitivity toward oxidative stress-induced cell death. Blood. 2009;113:3542–5.
Jönsson S, Lundberg AK, Jonasson L. Overexpression of MMP-9 and its inhibitors in blood mononuclear cells after myocardial infarction–is it associated with depressive symptomatology? PLoS ONE. 2014;9:e105572.
Mougiakakos D, Johansson CC, Jitschin R, Böttcher M, Kiessling R. Increased thioredoxin-1 production in human naturally occurring regulatory T cells confers enhanced tolerance to oxidative stress. Blood. 2011;117:857–61.
Holvoet P, Vanhaecke J, Janssens S, Van de Werf F, Collen D. Oxidized LDL and malondialdehyde-modified LDL in patients with acute coronary syndromes and stable coronary artery disease. Circulation. 1998;98:1487–94.
Itabe H. Oxidized low-density lipoprotein as a biomarker of in vivo oxidative stress: from atherosclerosis to periodontitis. J Clin Biochem Nutr. 2012;51:1–8.
Li W, Lidebjer C, Yuan XM, Szymanowski A, Backteman K, Ernerudh J, Leanderson P, Nilsson L, Swahn E, Jonasson L. NK cell apoptosis in coronary artery disease: relation to oxidative stress. Atherosclerosis. 2008;199:65–72.
Xie L, Pandey R, Xu B, Tsaprailis G, Chen QM. Genomic and proteomic profiling of oxidative stress response in human diploid fibroblasts. Biogerontology. 2009;10:125–51.
Taams LS, Smith J, Rustin MH, Salmon M, Poulter LW, Akbar AN. Human anergic/suppressive CD4(+)CD25(+) T cells: a highly differentiated and apoptosis-prone population. Eur J Immunol. 2001;31:1122–31.
Vukmanovic-Stejic M, Zhang Y, Cook JE, Fletcher JM, McQuaid A, Masters JE, Rustin MH, Taams LS, Beverley PC, Macallan DC, Akbar AN. Human CD4+ CD25hi Foxp3+ regulatory T cells are derived by rapid turnover of memory populations in vivo. J Clin Invest. 2006;116:2423–33.
Plaza-Sirvent C, Schuster M, Neumann Y, Heise U, Pils MC, Schulze-Osthoff K, Schmitz I. c-FLIP expression in Foxp3-expressing cells is essential for survival of regulatory T cells and prevention of autoimmunity. Cell Rep. 2017;18:12–22.
Zhang X, Zhang S, Liu X, Wang Y, Chang J, Zhang X, Mackintosh SG, Tackett AJ, He Y, Lv D, et al. Oxidation resistance 1 is a novel senolytic target. Aging Cell. 2018;17:e12780.
Söderberg A, Sahaf B, Rosén A. Thioredoxin reductase, a redox-active selenoprotein, is secreted by normal and neoplastic cells: presence in human plasma. Cancer Res. 2000;60:2281–9.
Apak R, Güçlü K, Ozyürek M, Karademir SE, Altun M. Total antioxidant capacity assay of human serum using copper(II)-neocuproine as chromogenic oxidant: the CUPRAC method. Free Radic Res. 2005;39:949–61.
Rubio CP, Hernández-Ruiz J, Martinez-Subiela S, Tvarijonaviciute A, Ceron JJ. Spectrophotometric assays for total antioxidant capacity (TAC) in dog serum: an update. BMC Vet Res. 2016;12:166.
Belikov AV, Schraven B, Simeoni L. T cells and reactive oxygen species. J Biomed Sci. 2015;22:85.
Muri J, Heer S, Matsushita M, Pohlmeier L, Tortola L, Fuhrer T, Conrad M, Zamboni N, Kisielow J, Kopf M. The thioredoxin-1 system is essential for fueling DNA synthesis during T-cell metabolic reprogramming and proliferation. Nat Commun. 1851;2018:9.
We would like to thank Mona Börjesson for her assistance in data collection. We are also especially grateful to all study participants for their willingness to participate in this study.
Open access funding provided by Linköping University. This study was financially supported by Heart-Lung Foundation, Sweden (20180436), Swedish Research Council (2018-03232), and Swedish Grandlodge of Freemasonry (20191209-141318).
Ethics approval and consent to participate
The study was conducted in accordance with the ethical guidelines of the Declaration of Helsinki, and the research protocol was approved by the Ethical Review Board of Linköping, Sweden (M242-08). Written informed consent was obtained from all study participants.
Consent for publication
The authors declare that they have no competing interests.
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. Representative flow cytometry images of Treg cells defined as CD4+CD127lowCD25+ (A) and Tconv cells defined as CD4+CD127+CD25− T cells (B) sorted with the EasySep Human CD4+CD127lowCD25+ Regulatory T Cell Isolation Kit. Characteristics shown are from left to right: forward and side scatter, CD4+ signal, CD25+ signal, and CD127+ signal. The expression of Foxp3 in Treg and Tconv cells sorted with the EasySep Human CD4+CD127lowCD25+ Regulatory T Cell Isolation Kit is shown in Figure C.
. Representative images for assessing sensitivity to ROS-induced cell death. The results from isolated Treg and Tconv cells are shown from the left to the right; untreated, treated with 10 µM H2O2 or treated with 30 µM H2O2. Annexin V and SYTOX signals are shown on the x and y axis, respectively. Regions include double-negative (S−−), Annexin V positive (S+−), SYTOX positive (S−+), and double-positive (S++). Since it is difficult to completely separate the transition from apoptosis to necrosis with this method, cells negative for both Annexin-V and SYTOX were considered viable.
The amount of oxidative stress, measured as mean fluorescence intensity (MFI) of CellROX Green, in (A) Treg cells from CCS patients and controls and (B) Tconv cells from CCS patients and controls following treatment with 0, 10, 30, 60 or 120 µM H2O2 for 2 h.
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Lundberg, A.K., Chung, R.W.S., Zeijlon, L. et al. Oxidative stress response in regulatory and conventional T cells: a comparison between patients with chronic coronary syndrome and healthy subjects. J Transl Med 19, 241 (2021). https://doi.org/10.1186/s12967-021-02906-2
- Coronary artery disease
- Chronic coronary syndrome
- T cell
- Regulatory T cell
- Oxidative stress