- Open Access
Decreased T helper 17 cells in tuberculosis is associated with increased percentages of programmed death ligand 1, T helper 2 and regulatory T cells
- Chin-Chung Shu†1, 2, 3,
- Ming-Fang Wu†4,
- Jann-Yuan Wang3,
- Hsin-Chih Lai5,
- Li-Na Lee3, 6,
- Bor-Luen Chiang7, 8Email author and
- Chong-Jen Yu3
© The Author(s). 2017
- Received: 10 January 2017
- Accepted: 9 May 2017
- Published: 26 June 2017
Tuberculosis (TB) is one of the most common infectious diseases worldwide. During active tuberculosis, T helper (Th) 17 cells are decreased, however the association with inhibitory immune regulation is unclear.
We enrolled 27 patients with TB and 20 age- and sex-matched controls and studies their lymphocyte status. Peripheral blood lymphocytes were isolated and programmed death-1 (PD-1) and programmed death ligand 1 (PD-L1) were measured on Th17 cells by using flow cytometry after the cells were stimulated with phorbol 12-myristate 13-acetate and ionomycin for 6 h. In addition, Th2 and regulatory T cells were measured and analyzed.
The TB group had lower levels of Th17 cells but higher levels of Th2 and Treg cells than the controls. In Th17 cells, the percentage of PD-L1 was higher in the TB group than that in the controls. In Th2 and Treg cells, the percentage of cytotoxic T-lymphocyte associated protein 4 (CTLA-4) was lower in the TB group and PD-1 was higher in Treg cells in the TB group. In the patients with extra-pulmonary TB, levels of Th1, Th2 and T17 cells were lower than those with pulmonary TB. The percentage of PD-1 on Th1 lymphocytes positively correlated with radiographic score.
Lower level of Th17 in TB patients may be associated with increased percentage of PD-L1 and increasing levels of Th2 and Treg cells which influenced by CTLA-4.
- Programmed cell death 1
- Cytotoxic T-lymphocyte-associated protein 4
- Th17 cells
- Regulatory T cells
- Th2 cells
Tuberculosis (TB) is the most important infectious disease worldwide. According to the World Health Organization, 300 million people are infected with Mycobacterium tuberculosis, and 30 million people with TB died from 2001 to 2010 [1, 2]. Timely treatment is one of the most important strategies to prevent further transmission of TB [3–5]. In addition to clinical judgment, understanding the immune process during active TB is important for clinical prediction of outcome and search of future target therapy.
In the pathogenesis of TB, adaptive immunity plays a pivotal role in primary TB and its reactivation. T helper (Th) 17 cells are an important type of lymphocyte that can establish protective immunity to TB in addition to Th1 cells, and they have been shown to have a significant pro-inflammatory effect in protecting against intracellular pathogens . Th17-related cytokines including IL-17 and IL-23 have been shown to be important for the early control of TB infection [7, 8]. However, it has recently been reported that the level of Th17 cells becomes lower in patients with TB infection , and the reason is not clear in regard to programmed cell death.
M. tuberculosis infection leads to the apoptosis of CD4+ T lymphocytes through interactions between programmed cell death ligand-1 (PD-L1) from dendritic cells and PD-1 on T cells . PD-1 is a member of the extended CD28 family of T cell regulators, and the intracellular tail contains two phosphorylation sites located in an immunoreceptor, which negatively regulate signals from T cell receptors . The percentage of PD-1 on CD4 T lymphocytes has been reported to be higher in patients with active TB, and that this may induce T cell malfunction . In Th17 cells, the roles of PD-1, PD-L1 and other suppressing cells, like Th2 and Treg cells, in active TB have yet to be elucidated. Therefore, we conducted the present study to investigate associations between the percentages of PD-1 and PD-L1 and changes in Th17 cells in patients with active TB.
This prospective study was conducted at National Taiwan University Hospital from January 2014 to August 2016. Patients aged ≥20 years who were diagnosed with active TB were recruited. Active TB was diagnosed by cultures positive for Mycobacterium tuberculosis or a typical pathology of Mycobacterium tuberculosis infection or suspicious radiographic findings plus a positive response to empirical TB treatment [4, 13]. In addition, we recruited age- and sex-matched controls with negative sputum cultures for mycobacteria. Patients with human immunodeficiency virus (HIV) infection, autoimmune diseases under regular chemotherapy, and those with a bleeding tendency that increased the risk of blood sampling were excluded.
The Research Ethics Committee of National Taiwan University Hospital approved this study (IRB No: 201312043RINB). All of the participants provided written informed consent, and the methods were carried out in accordance with the approved guidelines.
Isolation of peripheral blood mononuclear cells (PBMCs) or lymphocytes
Peripheral blood from the enrolled subjects was sampled into heparin-containing tubes. Mononuclear cells were immediately isolated using Ficoll-Paque PLUS (GE Healthcare Life Sciences, Sweden), and were then suspended in medium containing RPMI-1640 (Life Technologies; USA), 10% fetal bovine serum (FBS), and 1% penicillin-streptomycin (Life Technologies, USA). We isolated lymphocytes by negative selection using CD14-positive selection system (MACS system, Miltneyi Biotec Inc.) if PBMCs was more than 5 x 106 cell/mm3. Otherwise, we used PBMCs for further experiments for avoiding cells loss during lymphocyte selection. The intracellular cytokine responses in CD14-negative lymphocytes were similar to those in PBMCs, which were lower than those in peripheral blood leukocytes (Additional file 1: Figure S1, supplement file). All cells were immediately frozen using a CELL-BANKER system (ZENOAQ, Japan) following the manufacturer’s instructions. The cells were then stored at -80 °C and defrosted within days of the scheduled experiments. Before the experiments, viable cells were counted using a Scepter™ 2.0 Handheld Automated Cell Counter (Millipore Corporation, Billerica, MA, USA).
RNA isolation and real-time polymerase chain reaction
Total cellular RNA was extracted from peripheral blood lymphocytes after 6 h of stimulation with phorbol 12-myristate 13-acetate (50 uM) and Ionomycin (10 uM) using a Direct-zol™ RNA MiniPrep kit (Zymo Research, CA, USA) according to the manufacturer’s instructions. First-strand cDNA was synthesized using an iScriptTM cDNA Synthesis kit (Life Science Research, USA). A real-time polymerase chain reaction (PCR) with iQ SYBR Green Supermix (BIO-RAD, Singapore) was performed with 4.5 ng of cDNA using a Bio-Rad MyiQ Single-Color Real-Time PCR Detection System, and analyzed using Bio-Rad iQ5 Optical System 2.0 (Bio-Rad, CA). PCR mixtures were denatured at 95 °C for 5 min, followed by 40 cycles of 15 s at 95 °C, 30 s at 58 °C, and 30 s at 72 °C for amplification. The sense and antisense primers of IFN-γ (forward, 5’-ATT CGG TAA CTG ACT TGA ATG TCC-3’; reverse, 5’-CTC TTC GAC CTC GAA ACA GC-3’), IL-17 (forward, 5’-ATC TCC ACC GCA ATG AGG AC-3’; reverse, 5’-GTG G.AC AAT CGG GGT GACAC-3’), and GAPDH (forward, 5’-CCT CAA GAT CAT CAG CAA TG-3’; reverse, 5’-CAC GAT ACC AAA GTT GTC AT -3’) were applied. The mRNA expression level of each target gene was normalized to the respective GAPDH expression.
Flow cytometry for PBMCs or peripheral blood lymphocytes
The PBMCs or peripheral blood lymphocytes were cultivated in 96-well plates in 300 μl of RPMI 1640 medium with 10% Fetal bovine serum and 1% penicillin-streptomycin (2 x 105 cells per well). Phorbol 12-myristate 13-acetate (50 ng/ml, TOCRIS, USA), and ionomycin calcium salt (1 μM/ml, Sigma-Aldrich, USA) were added to enhance the levels of cytokines because intracellular cytokine staining yielded a very low percentage (Additional file 1: Figure S1, supplement file) at baseline without stimulation. Protein transport inhibitor (BD Bioscience, USA) was added to the co-culture. The peripheral blood lymphocytes were retrieved after 6 h of reaction and measured using flow cytometry (FACSVerse, BD Biosciences, USA). We measured the level of CD4+ T cells using anti-CD4-APC, and stained different types of T cells with anti-IFN-γ-PerCP, anti-IL-4-PerCP, anti-17A-PE, anti-CD25-FITC, anti-Foxp3-PerCP, anti-TNF-α-PerCP antibodies (BD Biosciences, CA, USA). Anti-PD-1-PEcy7.0 (used together with anti-IFN and anti-IL-17A), anti-PD-1-PE (used for other staining antibodies), anti-PD-L1-FITC, and anti-cytotoxic T-lymphocyte associated protein 4 (CTLA-4)-PEcy7.0 (eBiosciences, USA) were used to examine the percentages of PD-1, PD-L1 and CTLA-4 on T cells. Data were analyzed using BD FACSuite V software (BD, Biosciences, USA). We discriminated the lymphocyte population using forward scatter (FSC) and side scatter (SSC). Within the group, we gated the subgroups of different T lymphocyte and measured the percentage of PD-1, PD-L1 and CTLA-4 respectively.
Data collection and statistical analysis
Clinical data including age, sex, co-morbidities, radiographic findings and laboratory data at enrollment were recorded in a standardized case report form with default options. Inter-group differences were analyzed using the Student’s t-test or Mann-Whitney U test for numerical variables, where appropriate. The chi-square test was used for categorical variables. Statistical significance was set at p < 0.05. All analyses were performed using SPSS version 19.0 (Chicago, IL).
A total of 27 patients (20 [74%] males) with active TB were enrolled, with an average age of 50.1 years (standard deviation [SD]: 16.8). We also enrolled 20 controls (12 [60%] males), with an average age of 56.1 (SD: 12.5) years. There were no significant differences in age and sex between the TB and control groups (p = 0.193, and 0.317, respectively). Among the TB group, 18 (67%) patients had pulmonary TB, six (22%) had concurrent pulmonary and extra-pulmonary TB, and three (11%) had extra-pulmonary TB only. With regards to the patients with extra-pulmonary TB, five had lymphadenitis, three had pleurisy, and one had spleen involvement. With regards to the diagnosis of TB, 20 patients had culture-confirmed TB including 10 with a typical pathology for TB, six were diagnosed according to a typical pathology, and the remaining one by typical chest imaging and response to empirical TB treatment. Four patients had an underlying malignancy, and five had diabetes mellitus.
In the present study, we observed changes in T lymphocytes in patients with active TB infection, and found a lower percentage Th17 cells but higher percentages of Th2 and Treg cells in the patients with active TB infection compared to the controls. In addition, the patients with extra-pulmonary TB had lower percentages of Th1, Th2, and Th17 cells but a similar percentage of Treg cells compared to those with pulmonary TB. The radiographic score was correlated with the percentage of PD-1 in CD4 or PD-1 on Th1 lymphocytes. With regards to the inhibitory effect of T cell receptors, the percentage of PD-L1 was higher in Th1 and Th17 cells, CTLA-4 was lower in Th2 and Treg cells, and PD-1 was higher in Treg cells in the patients with TB compared to the controls.
Th17 cells are classified as a CD4 T cell subset and are distinct from Th1 and Th2 subsets. Th17 cells produce the cytokines IL-17A and IL-17 F and can lead to a significant pro-inflammatory effect , and also protect against intracellular pathogens . Recent studies have reported that Th17 cells are involved in immunity against M. tuberculosis . However, the results of Th17 responses in the patients with TB are still inconsistent . A similar IL-17 mRNA expression has been observed in CD4+ blood cells between TB patients and healthy controls , and a higher percentage of IL-17+CD4+ lymphocytes at baseline  or after M. tuberculosis antigen stimulation has been observed in TB patients , whereas a lower percentage of blood IL-17+CD4+ cells has also been reported in TB patients [9, 16], similar with the present study. These discrepancies might be due to differences in ethnicity, stimulation antigen, or underlying host immunity and require future investigation.
Because a low level of IL-17 in the blood has been associated with a high rate of mortality in TB patients  and our observations showed attenuated IL-17+CD4+ cells in TB patients, we aimed to elucidate the reason for the attenuation of Th17 in TB. A reduced expression of IL-6 receptors on T cells has been postulated , and also that the Th17 response may be regulated by signal transducer and activator of transcription 3 and PD-1 signaling . However, associations between Th17 and PD-L1, Th2 and Treg cells have rarely been reported in TB.
In the present study, the percentage of Th17 was lower in the patients with active TB. Interestingly, the percentage of PD-1 in Th17 cells was similar between the TB and control groups, but PD-L1 was higher in the TB group. Although the percentages of PD-1 and PD-L1 have both been reported to be higher in CD4 lymphocytes in patients with TB , the percentage of PD-L1 has rarely been discussed in Th17 cells. In chronic mycobacterial infection, the PD-1 pathway, including PD-1 and its ligands, is induced and negatively regulates inflammatory processes [11, 23]. The increase in PD-L1 in Th17 cells may represent self-suppression among lymphocytes in the PD-1 pathway, as previously reported .
The percentage of Th2 cells was higher in the TB patients in this study, and was significantly correlated with Th17 cells in the TB group (Pearson correlation: 0.785, p < 0.001). The anti-inflammatory effect of Th2 cells may passively increase to counteract the induction of Th1/Th17 during TB infection, and the increase in PD-L1 in Th2 cells may be associated with the suppressive ability of Th2 cells . The trend of an increased percentage of Treg cells from the controls to the patients with TB was in contrast to the Th17 cells. Although the percentage of Treg cells was not correlated with Th17 cells, the percentage of PD-1 in Treg cells was well correlated with Th17 cells. The over-percentage of PD-1 in Treg cells can lead to enhanced function and population expansion in patients with TB , and this may play a suppressive role to attenuate the percentage of Th17 cells. In contrast, the percentage of CTLA-4 was lower in the Treg cells in the TB group leading to a less negative signaling, which also induced an expansion in its population .
With regards to the extent of disease, the percentages of Th1, Th2 and Th17 cells were lower in the patients with extra-pulmonary TB compared to those with pulmonary TB (Fig. 3) and might influenced the overall results in TB patients. The lower expression of Th1 cells in extra-pulmonary TB is not consistent with previous reports [27, 28] and might be explained by that more patients with extra-pulmonary TB had cancer in this study. On the other hand, the percentage of PD-1 has been reported to be higher in CD4 lymphocytes in patients with TB , although this was not observed in the present study. Possible explanations for this include the small number of cases, differences in ethnicity, and a higher number of cases diagnosed by pathology. In addition, 80% of samples in this study were blood lymphocytes and we used stimulation of PMA plus ionomycin, the results might not be compared similarly with previous study. However, the percentage of PD-1 in CD4 or Th1 lymphocytes was still associated with a high extent of disease, as defined by a higher radiographic score. This implies that the percentage of PD-1 is induced by TB bacilli, and that it increases with disease progression.
There are several limitations to the present study. First, the number of cases was small, and making a firm conclusion and performing regression analysis were not possible. Second, patients had comorbidities of cancer and diabetes mellitus were included and the disease spectrum was heterogeneous Both factors might have influenced the immune responses [27–29]. Third, around 20% samples were PBMCs and might influence the results though there was not intergroup difference. However, the cytokine responses were higher in peripheral blood leukocytes than in PBMCs, and these results may have underestimated the cell responses. Last, the role of PD and PD-L1 on T helper cells remains unclear, and future investigations with blocking assays are required.
The percentage of Th17 cells was decreased in patients with TB, and an increased percentage of PD-L1 on Th17 cells was observed together with higher percentages of Th2 and Treg cells, which might be associated with the attenuation of Th17 cells. Further studies investigating the mechanism of PD-L1 in Th17 cells would be helpful to clarify the pathogenesis of TB. On the other hand, increasing percentage of PD-1 but decreasing CTLA-4 might be responsible for increasing Treg cells whereas lower CTLA-4 might correlate with higher Th2 cells in patients with TB. With regards to the extent of disease, the patients with extra-pulmonary TB had lower percentages of Th1, Th2, and Th17 cells and the patients with more pulmonary involvement had a higher percentage of PD-1 in Th1 lymphocytes. This suggests a complex immune response in patients with TB, and that the percentage of PD-1 in Th1 cells is important within TB process.
The authors thank the staff of the Seventh and Eighth Core Labs of the Department of Medical Research of National Taiwan University Hospital for their technical support.
This study was supported in part by grants from the Ministry of Science and Technology, Taiwan (MOST 103-2314-B-002 -152 -MY2; MOST 104-2314-B-002 -079 -MY3) and National Taiwan University Hospital (NTUH 105-S2999). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Availability of data and materials
Please contact author for data requests.
SCC, WMF, WJY, LHC, and LLN performed the experiments, data collection, data analysis and manuscript writing. CBL and YCJ were responsible for coordination. All authors read and approved the final manuscript.
All authors declare no financial, professional or other personal interest of any nature or kind in a related product, service, and/or company.
Consent for publication
Not applicable. The present study did not contain any individual person’s data in any form.
Ethics approval and consent to participate
The Research Ethics Committee of National Taiwan University Hospital approved this study (IRB No: 201312043RINB). All of the participants provided written informed consent.
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