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MTB-specific lymphocyte responses are impaired in tuberculosis patients with pulmonary cavities
European Journal of Medical Research volume 22, Article number: 4 (2017)
Tuberculosis (TB), an infectious disease caused by the bacillus Mycobacterium tuberculosis (MTB), is a global health problem. Because the failing immune response in the lung can lead to formation of a pulmonary cavity, this study was designed to clarify MTB-specific lymphocyte responses in TB patients with pulmonary cavities.
We utilized culture filtrate protein 10 (CFP-10) and early secretory antigenic target 6 (ESAT-6) as immunogenic MTB antigens following overnight stimulation of peripheral blood mononuclear cells (PBMCs). By flow cytometry, we then dissected CD4+ and CD8+ T lymphocytes secreting intracellular cytokines of IFN-γ and TNF-α to assess the local immune response of TB patients with pulmonary cavities compared with those having other radiological infiltrates.
As expected, after 16 h of ex vivo activation using both ESAT-6 and CFP-10, the proportions of CD4+IFN-γ, CD4+TNF-α, CD8+TNF-α, and CD8+IFN-γ cells were all markedly increased in 46 patients with TB when compared with 23 household contacts. However, the IFN-γ and TNF-α responses of both CD4+ and CD8+ T lymphocytes were found to be relatively lower in 18 patients who had pulmonary cavities when compared with 28 patients who had radiological infiltrates. Moreover, patients with cavities had higher absolute numbers of neutrophils than patients with infiltrates. Further analysis indicated an inverse correlation between neutrophil counts and the proportions of IFN-γ-secreting T cells.
MTB-specific lymphocyte responses are impaired in TB patients with pulmonary cavities that are likely to play an important role in the pathogenesis of cavitary TB.
Tuberculosis (TB), an infectious disease caused by the bacillus Mycobacterium tuberculosis (MTB), is a global health problem. Overall, a relatively small proportion (5–15%) of the estimated 2–3 billion people infected with MTB will develop TB disease during their lifetimes . However, the probability of developing TB is much higher among people infected with human immunodeficiency virus (HIV), indicating that the adaptive immune response plays a vital role in controlling MTB pathogenesis. The components of this protective immune response have been investigated with an emphasis on the role of T cells secreting type-1 cytokines, specifically TNF-α and IFN-γ, in the formation of granulomas in the lung [2–6].
However, a failing immune response in the lung may be involved in the formation of pulmonary cavities. With regard to the TNF-α and IFN-γ responses of cavitary TB, several investigators have produced conflicting results. Casarini noted only that IFN-γ but not TNF-α was reduced in cavities compared with areas of infiltrates as measured by ELISA , and Condos demonstrated similar results . However, Mazzarella pointed to a reduction in type-1 cytokines from both cavities and areas of infiltrates . Fan et al. also recently demonstrated that the MTB antigen-specific Th1 response was decreased when pulmonary TB (PTB) lesions developed in severe cavities .
T cells specific for multiple immunogenic antigens of MTB have recently been identified, including the Ag85 complex, culture filtrate protein 10 (CFP-10), early secretory antigenic target 6 (ESAT-6), heat shock protein 65, and TB10.4 [8–11]. In particular, ESAT-6 and CFP-10 have been utilized as antigens for the immune diagnosis of MTB infection based on the presence of IFN-secreting cells; both have been shown to be more specific and sensitive than tuberculin skin tests .
Flow cytometry (FCM) is a powerful technology for characterizing each cell in terms of both the intracellular cytokines, and also activation markers. In addition, FCM is better than enzyme-linked immunosorbent assay (ELISA) to detect cytokines in peripheral blood mononuclear cells (PBMCs) from patients with TB, because ELISA cannot reveal which specific cells are producing and secreting the measured cytokines.
To clarify MTB-specific lymphocyte responses in TB patients with pulmonary cavities, we utilized ESAT-6 and CFP-10 as immunogenic antigens and FCM to determine the blood lymphocyte responses of CD4+ and CD8+ T lymphocytes producing and secreting IFN-γ and TNF-α in order to study the local immune responses of subjects with cavitary disease as compared to individuals having pulmonary infiltrates.
Study subjects and ethics statement
Our study included 46 newly diagnosed patients with PTB and 23 household contacts from the physical examination center of our hospital with both TST and T-SPOT negative. All information on the patients was recorded in the clinical database of the Infectious Disease Hospital of Wuxi, China. PBMCs were isolated before treatment from blood samples by means of centrifugation with Ficoll-Hypaque (Sigma). PTB was diagnosed when subjects with clinical and/or imaging features compatible with TB met at least one of the following criteria: positive sputum smear for acid-fast bacilli; positive culture for MTB, biopsy suggestive of TB, and/or full response to anti-TB treatment. A radiologist reviewed the posteroanterior chest radiographs (CXRs) of all 48 newly diagnosed PTB patients for the presence or absence of cavities. A respiratory clinician reviewed all CXRs at the same time, with both agreeing on the results.
Peptides (16- to 18-mers overlapping by 10 aa) corresponding to the sequence of the MTB antigens CFP-10 and ESAT-6 were synthesized on an automated peptide synthesizer. For initial screening purposes, peptides were arranged into pools of 9 peptides each in matrix fashion, such that each peptide was uniquely represented in 2 pools .
Intracellular cytokine staining and immunophenotyping
PBMCs were isolated from heparin anticoagulant whole blood and incubated with stimulated antigens using 200 μL of per stimulation in a polypropylene tube. Each patient had four different stimulation setups: negative (medium alone), positive [Phorbol 12-myristate 13-acetate (PMA), each at 5 mg/mL], CFP-10 (10 mg/mL), and ESAT-6 (10 mg/mL). Tubes were vortexed, covered, and kept overnight (16 h) at 37 °C in a 5% CO2 incubator. In addition, 10 μg of Brefeldin A (Sigma) was added after 2 h of incubation. Following overnight stimulation, the cells were washed and stained with the following surface antibodies at room temperature for 15 min: energy-coupled dye (ECD)-conjugated anti-CD3 and fluorescein isothiocyanate (FITC)-conjugated anti-CD8. The cells were washed, fixed, and permeabilized (with Caltag reagents A and B) (Caltag Laboratories). The following intracellular antibodies were then added: phycoerythrin–Cy5.5 (PE-Cy5.5)-conjugated anti-IFN-γ and phycoerythrin (PE)-conjugated TNF-α. All antibodies were purchased from Becton–Dickinson.
The cells were incubated for 15 min and then washed and placed on an FC500 (Beckman Coulter) flow cytometer. Negative controls consisting of PBMCs incubated with medium alone were included in each assay. Responses ≥0.03% above the background value were considered to be positive. For phenotypic analysis of CD8 cells, peptide-stimulated cells were gated on CD3+/CD8+ cells and analyzed for expression of TNF-α and IFN-γ. For phenotypic analysis of CD4 cells, peptide-stimulated cells were gated on CD3+/CD8− cells and analyzed for expression of TNF-α and IFN-γ.
Statistical analyses were conducted using GraphPad Prism software version 4.0. The unpaired, nonparametric t test (Mann–Whitney test), Chi square test, and Spearman rank correlation analysis were performed. Values of P < 0.05 were considered to be statistically significant for all analyses.
Characteristics of the study population
Our subjects included 46 newly treated TB patients, including 18 patients with cavitary TB, and 28 patients who presented with chest infiltrates on CT scanning. Among the 23 household contacts, there were 11 males and 12 females whose mean age was 50.1 ± 5.6 years. The clinical characteristics of the 46 TB patients and their laboratory data are summarized in Table 1. No significant differences were found regarding age, gender, absolute number of white blood cells (WBCs), monocytes and lymphocytes, or the proportions of CD3+, CD3+/CD4, and CD3+/CD8+ lymphocytes between 18 patients with chest cavities and 28 patients with infiltrates. However, there were significant differences with regard to the absolute number of neutrophils. Patients with cavities had higher absolute neutrophil counts than patients with infiltrates.
Increased percentages of MTB antigen-specific cytokine-producing T cells in TB patients
We stained cells for identification by FCM and then tested the proportions of IFN-γ- and TNF-α-producing CD4+ and CD8+ T cells after cells were cultured and stimulated with ESAT-6 and CFP-10, respectively. Results are presented in Table 2. As expected, the percentages of IFN-γ and TNF-α produced by CD4+ and CD8+ T cells after stimulation with ESAT-6 and CFP-10 were significantly higher in TB patients than in household contacts (P values all <0.05).
Impaired MTB antigen-specific responses of CD4+ and CD8+ T lymphocytes in PTB patients with cavities
MTB-specific responses of CD4+ and CD8+ T lymphocytes from TB patients measured by intracellular TNF-α and IFN-γ staining after overnight incubation were shown as FCM dot plots (Fig. 1a, b). TB patients were divided into two groups; on computed tomography (CT) of the chest, 18 patients presented with cavities and the 28 others with infiltrates. The result showed that the TNF-α and IFN-γ produced by CD4+ and CD8+ T lymphocytes in response to ESAT-6 and CFP-10 in the patients with cavities were statistically reduced compared with the radiological infiltrates (P values all <0.05) (Fig. 1c, d). The data on the TB patients with cavities and the household contacts were equally low, with P > 0.05 (not shown).
Inverse correlation between the proportions of MTB-specific IFN-γ-secreting T cells and neutrophil counts
To further determine the impact of high absolute neutrophil counts in patients with cavities on the impaired MTB antigen-specific responses, we analyzed the relationship between the proportions of MTB antigen-specific IFN-γ- and TNF-α-secreting T cells (CD4+ and CD8+) with neutrophil counts in all TB patients and found no correlation between TNF-α-secreting T cells with neutrophil counts (Fig. 2a, c). However, both IFN-γ-producing CD4+ and CD8+ T cells had significant inverse correlations with neutrophil counts (R = −0.2809, P = 0.007; R = −0.2098, P = 0.0447, respectively) (Fig. 2b, d).
Type-1 immune dominance during TB was shown by the predominance of CD4+ and CD8+ T cells responsive to MTB antigens by rapid IFN-γ and TNF-α synthesis. These cells were found in both radiologically involved and uninvolved pulmonary sites but were conspicuously reduced in areas of cavity formation . Our results indicate that proportions of TNF-α- and IFN-γ-producing cells within both the CD4+ and CD8+ subsets were significantly reduced in TB patients with cavities compared with those with radiological infiltrates after stimulation of ESAT-6 or CFP-10, respectively, although the activities of IFN-γ and TNF-α were broad and included both beneficial and detrimental effects . IFN-γ and TNF-α may help to recruit cells to the site of infection and promote the antimicrobial activity of macrophages [16, 17]. In addition, TNF-α can lead to TNF-mediated apoptosis of infected macrophages, thus helping to eliminate the pathogen . Therefore, type-1 cytokines, IFN-γ and TNF-α, may generate protective granulomas and enhance the killing of MTB within macrophages.
However, the IFN-γ and TNF-α responses of both CD4+ and CD8+ T lymphocytes from TB patients were remarkably impaired in those individuals with pulmonary cavities. The pulmonary cavity has been the classic hallmark of TB and is the site of a very high MTB burden. MTB infection triggers the recruitment of leukocytes and the activation of intercellular networks, which then results in tissue destruction . Successful immune responses lead to the formation of granulomas and curtailment of the disease process, whereas cavitation indicates a failing immune response . Histological examination also demonstrates a predominance of acid-fast bacilli only at the internal surfaces of the cavities, at which site there are few CD4 and CD8 lymphocytes . The pulmonary cavities are the sites of high MTB burdens.
Cavitation has also been reported to be associated with local neutrophilia and relative lymphopenia . Our results show that TB patients with cavities had higher absolute numbers of neutrophils than did patients with infiltrates; moreover, further analysis indicated an inverse correlation between the proportions of MTB-specific IFN-γ-secreting T cells and neutrophil counts. The accumulation of neutrophils together with these impaired MTB-specific lymphocyte responses probably plays an important role in the pathogenesis of cavitary TB.
Our study also has limitations. The eligible patients represented a fraction of the patients diagnosed with active TB, raising a concern for a selection bias. The antigen of CD4 was endocytosed with the stimulation of PMA and also impaired by the process of permeabilization. Therefore for the phenotypic analysis of CD4 cells, peptide-stimulated cells were gated on CD3+ CD8− cells. Except for these limitations, we conclude that MTB-specific lymphocyte responses are impaired in TB patients with pulmonary cavities, which may explain the high MTB burden at the cavity site and the severity of cavitary.
MTB-specific lymphocyte responses are impaired in TB patients with pulmonary cavities that are likely to play an important role in the pathogenesis of cavitary TB.
- MTB :
culture filtrate protein 10
early secretory antigenic target 6
enzyme linked immunoabsorbant assays
peripheral blood mononuclear cells
phorbol myfismte acetate
white blood cell
World Health Organization. Global tuberculosis report 2015. Geneva: World Health Organization; 2015.
Newport MJ, Huxley CM, Huston S, Hawrylowicz CM, Oostra BA, Williamson R, et al. A mutation in the interferon-gamma-receptor gene and susceptibility to mycobacterial infection. N Engl J Med. 1996;335(26):1941–9.
Chackerian AA, Perera TV, Behar SM. Gamma interferon-producing CD4+ T lymphocytes in the lung correlate with resistance to infection with Mycobacterium tuberculosis. Infect Immun. 2001;69(4):2666–74.
Casarini M, Ameglio F, Alemanno L, Zangrilli P, Mattia P, Paone G, et al. Cytokine levels correlate with a radiologic score in active pulmonary tuberculosis. Am J Respir Crit Care Med. 1999;159(1):143–8.
Condos R, Rom WN, Liu YM, Schluger NW. Local immune responses correlate with presentation and outcome in tuberculosis. Am J Respir Crit Care Med. 1998;157(3 Pt 1):729–35.
Mazzarella G, Bianco A, Perna F, D’Auria D, Grella E, Moscariello E, et al. T lymphocyte phenotypic profile in lung segments affected by cavitary and non-cavitary tuberculosis. Clin Exp Immunol. 2003;132(2):283–8.
Fan Lin, Xiao Heping, Mai Guangliang, Bo Su, Ernst Joel, Zhongyi Hu. Impaired M. tuberculosis antigen-specific IFN-γ response without IL-17 enhancement in patients with severe cavitary pulmonary tuberculosis. PLoS ONE. 2015;10(5):e0127087.
Valle MT, Megiovanni AM, Merlo A, Pira GL, Bottone L, Angelini G, et al. Epitope focus, clonal composition and Th1 phenotype of the human CD4 response to the secretory mycobacterial antigen Ag85. Clin Exp Immunol. 2001;123(2):226–32.
Pathan AA, Wilkinson KA, Klenerman P, McShane H, Davidson RN, Pasvol G, et al. Direct ex vivo analysis of antigen-specific IFN-γ-secreting CD4 T cells in Mycobacterium tuberculosis-infected individuals: associations with clinical disease state and effect of treatment. J Immunol. 2001;167(9):5217–25.
Pathan AA, Wilkinson KA, Wilkinson RJ, Latif M, McShane H, Pasvol G, et al. High frequencies of circulating IFN-γ-secreting CD8 cytotoxic T cells specific for a novel MHC class I-restricted Mycobacterium tuberculosis epitope in M. tuberculosis infected subjects without disease. Eur J Immunol. 2000;30(9):2713–21.
Ravn P, Demissie A, Eguale T, Wondwosson H, Lein D, Amoudy HA, et al. Human T cell responses to the ESAT-6 antigen from Mycobacterium tuberculosis. J Infect Dis. 1999;179(3):637–45.
Pai M, Riley LW, Colford JM Jr. Interferon-assays in the immunodiagnosis of tuberculosis: a systematic review. Lancet Infect Dis. 2004;4(12):761–6.
Addo MM, Yu XG, Rathod A, Cohen D, Eldridge RL, Strick D, et al. Comprehensive epitope analysis of human immunodeficiency virus type 1 (HIV-1)-specific T-cell responses directed against the entire expressed HIV-1 genome demonstrate broadly directed responses, but no correlation to viral load. J Virol. 2003;77(3):2081–92.
Barry S, Breen R, Lipman M, Johnson M, Janossy G. Impaired antigen-specific CD4+ T lymphocyte responses in cavitary tuberculosis. Tuberculosis. 2009;89(1):48–53.
Pfeffer K. Biological functions of tumor necrosis factor cytokines and their receptors. Cytokine Growth Factor Rev. 2003;14(3/4):185–91.
Flynn JL, Goldstein MM, Chan J, Triebold KJ, Pfeffer K, Lowenstein CJ, Schreiber R, et al. Tumor necrosis factor-alpha is required in the protective immune response against Mycobacterium tuberculosis in mice. Immunity. 1995;2(6):561–72.
Chakravarty SD, Zhu G, Tsai MC, Mohan VP, Marino S, Kirschner DE, Huang L, et al. Tumor necrosis factor blockade in chronic murine tuberculosis enhances granulomatous inflammation and disorganizes granulomas in the lungs. Infect Immun. 2008;76(3):916–26.
Ong CW, Elkington PT, Friedland JS. Tuberculosis, pulmonary cavitation, and matrix metalloproteinases. Am J Respir Crit Care Med. 2014;190(1):9–18.
Kaplan G, Post FA, Moreira AL, Wainwright H, Kreiswirth BN, Tanverdi M, et al. Mycobacterium tuberculosis growth at the cavity surface: a microenvironment with failed immunity. Infect Immun. 2003;71(12):7099–108.
HP and JW conceived and designed the experiments. JW, JL and YD performed the experiments. JW analyzed the data. All authors read and approved the final manuscript.
We thank the all patients for their support in this research and colleagues of The Fifth People’s Hospital of Wuxi for their assistance in collection of research data.
The authors declare that they have no competing interests.
Availability of data and materials
The datasets analyzed during the current study available from the corresponding author on reasonable request.
Consent for publication
Written patient consents were obtained for publication in European Journal of Medical Research.
Ethics approval and consent to participate
This study was approved by the Institutional Ethics Committee of Infectious Hospital of Wuxi, Affiliated to Jiangnan University (No: WXIH2015-012), and was in compliance with the national legislation and the Declaration of Helsinki guidelines. Written patient consents were obtained according to the institutional guidelines.
This work was supported by Health Bureau of Wuxi, China (Nos. Z201405 and Q201506), Science and Technology Bureau of Wuxi, China (No. CSEOIN1226), Hospital management center of Wuxi, China (No. YGZXM1523).
Jun Wang, Yaping Dai and Jun Liu contributed equally to this work
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Wang, J., Dai, Y., Liu, J. et al. MTB-specific lymphocyte responses are impaired in tuberculosis patients with pulmonary cavities. Eur J Med Res 22, 4 (2017). https://doi.org/10.1186/s40001-016-0242-9